Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
17	g.7669589_7676614del	CA2499224945	TP53	c.-19_21del c.-21-1377_21del c.-19_310del c.-19_222del c.-253_21del c.-136_222del c.-136_21del c.-136_310del c.-136_983+1021del	ClinVar
17	g.7669609_7676594del	CA2581463470	TP53	c.1_1182del c.-21-1358_786del c.1_903del c.1_1161del c.1_994-3365del c.1_782+4572del c.1_289del c.1_201del c.-234_1065del c.-117_201del c.1_1149del c.-117_1065del c.-117_289del c.-117_983+1000del
17	g.7673592_7673702del	CA645587377	TP53	c.919+1_938del c.523+1_542del c.640+1_659del c.898+1_917del c.782+481_782+591del (n.782+481_782+591del) c.802+1_821del c.442+1_461del c.886+1_905del	COSMIC
17	g.7673598_7673702del	CA645587380	TP53	c.919_931del c.523_535del c.640_652del c.898_910del c.782+480_782+584del (n.782+480_782+584del) c.802_814del c.442_454del c.886_898del	COSMIC
17	g.7673611_7673702del	CA2556749014	TP53	c.919+1_920-1del c.523+1_524-1del c.640+1_641-1del c.898+1_899-1del c.782+481_782+572del (n.782+481_782+572del) c.802+1_803-1del c.442+1_443-1del c.886+1_887-1del
17	g.7673611_7673649del	CA645587393	TP53	c.920-41_920-3del (n.920-41_920-3del) c.524-41_524-3del (n.524-41_524-3del) c.641-41_641-3del (n.641-41_641-3del) c.899-41_899-3del (n.899-41_899-3del) c.782+532_782+570del (n.782+532_782+570del) c.803-41_803-3del (n.803-41_803-3del) c.443-41_443-3del (n.443-41_443-3del) c.887-41_887-3del (n.887-41_887-3del)	COSMIC COSMIC COSMIC
17	g.7673635_7673845del	CA645587395	TP53	c.783-8_920-27del c.387-8_524-27del c.504-8_641-27del c.762-8_899-27del c.782+336_782+546del (n.782+336_782+546del) c.666-8_803-27del c.306-8_443-27del c.750-8_887-27del	COSMIC
17	g.7673645C>A	CA2733129864	TP53	c.920-37G>T (n.920-37G>T) c.524-37G>T (n.524-37G>T) c.641-37G>T (n.641-37G>T) c.899-37G>T (n.899-37G>T) c.782+536G>T (n.782+536G>T) c.803-37G>T (n.803-37G>T) c.443-37G>T (n.443-37G>T) c.887-37G>T (n.887-37G>T)	dbSNP
17	g.7673645C>G	CA2733129867	TP53	c.920-37G>C (n.920-37G>C) c.524-37G>C (n.524-37G>C) c.641-37G>C (n.641-37G>C) c.899-37G>C (n.899-37G>C) c.782+536G>C (n.782+536G>C) c.803-37G>C (n.803-37G>C) c.443-37G>C (n.443-37G>C) c.887-37G>C (n.887-37G>C)	dbSNP
17	g.7673645C>T	CA2733129861	TP53	c.920-37G>A (n.920-37G>A) c.524-37G>A (n.524-37G>A) c.641-37G>A (n.641-37G>A) c.899-37G>A (n.899-37G>A) c.782+536G>A (n.782+536G>A) c.803-37G>A (n.803-37G>A) c.443-37G>A (n.443-37G>A) c.887-37G>A (n.887-37G>A)	dbSNP
17	g.7673646T>A	CA2732931321	TP53	c.920-38A>T (n.920-38A>T) c.524-38A>T (n.524-38A>T) c.641-38A>T (n.641-38A>T) c.899-38A>T (n.899-38A>T) c.782+535A>T (n.782+535A>T) c.803-38A>T (n.803-38A>T) c.443-38A>T (n.443-38A>T) c.887-38A>T (n.887-38A>T)	dbSNP
17	g.7673646T>C	CA001271	TP53	c.920-38A>G (n.920-38A>G) c.524-38A>G (n.524-38A>G) c.641-38A>G (n.641-38A>G) c.899-38A>G (n.899-38A>G) c.782+535A>G (n.782+535A>G) c.803-38A>G (n.803-38A>G) c.443-38A>G (n.443-38A>G) c.887-38A>G (n.887-38A>G)	dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673646T=	CA2245948176	TP53	c.920-38A= (n.920-38A=) c.524-38A= (n.524-38A=) c.641-38A= (n.641-38A=) c.899-38A= (n.899-38A=) c.782+535A= (n.782+535A=) c.803-38A= (n.803-38A=) c.443-38A= (n.443-38A=) c.887-38A= (n.887-38A=)
17	g.7673647G>A	CA001278	TP53	c.920-39C>T (n.920-39C>T) c.524-39C>T (n.524-39C>T) c.641-39C>T (n.641-39C>T) c.899-39C>T (n.899-39C>T) c.782+534C>T (n.782+534C>T) c.803-39C>T (n.803-39C>T) c.443-39C>T (n.443-39C>T) c.887-39C>T (n.887-39C>T)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673647G>C	CA2732929148	TP53	c.920-39C>G (n.920-39C>G) c.524-39C>G (n.524-39C>G) c.641-39C>G (n.641-39C>G) c.899-39C>G (n.899-39C>G) c.782+534C>G (n.782+534C>G) c.803-39C>G (n.803-39C>G) c.443-39C>G (n.443-39C>G) c.887-39C>G (n.887-39C>G)	dbSNP
17	g.7673647G=	CA2245948178	TP53	c.920-39C= (n.920-39C=) c.524-39C= (n.524-39C=) c.641-39C= (n.641-39C=) c.899-39C= (n.899-39C=) c.782+534C= (n.782+534C=) c.803-39C= (n.803-39C=) c.443-39C= (n.443-39C=) c.887-39C= (n.887-39C=)
17	g.7673647G>T	CA2732929151	TP53	c.920-39C>A (n.920-39C>A) c.524-39C>A (n.524-39C>A) c.641-39C>A (n.641-39C>A) c.899-39C>A (n.899-39C>A) c.782+534C>A (n.782+534C>A) c.803-39C>A (n.803-39C>A) c.443-39C>A (n.443-39C>A) c.887-39C>A (n.887-39C>A)	dbSNP
17	g.7673648A>C	CA656753439	TP53	c.920-40T>G (n.920-40T>G) c.524-40T>G (n.524-40T>G) c.641-40T>G (n.641-40T>G) c.899-40T>G (n.899-40T>G) c.782+533T>G (n.782+533T>G) c.803-40T>G (n.803-40T>G) c.443-40T>G (n.443-40T>G) c.887-40T>G (n.887-40T>G)	COSMIC
17	g.7673648A>G	CA2733129876	TP53	c.920-40T>C (n.920-40T>C) c.524-40T>C (n.524-40T>C) c.641-40T>C (n.641-40T>C) c.899-40T>C (n.899-40T>C) c.782+533T>C (n.782+533T>C) c.803-40T>C (n.803-40T>C) c.443-40T>C (n.443-40T>C) c.887-40T>C (n.887-40T>C)	dbSNP
17	g.7673648_7673717del	CA645587396	TP53	c.903_920-40del c.507_524-40del c.624_641-40del c.882_899-40del c.782+464_782+533del (n.782+464_782+533del) c.786_803-40del c.426_443-40del c.870_887-40del	COSMIC
17	g.7673649G>A	CA2635874467	TP53	c.920-41C>T (n.920-41C>T) c.524-41C>T (n.524-41C>T) c.641-41C>T (n.641-41C>T) c.899-41C>T (n.899-41C>T) c.782+532C>T (n.782+532C>T) c.803-41C>T (n.803-41C>T) c.443-41C>T (n.443-41C>T) c.887-41C>T (n.887-41C>T)	dbSNP gnomAD v4
17	g.7673649G>C	CA2733129880	TP53	c.920-41C>G (n.920-41C>G) c.524-41C>G (n.524-41C>G) c.641-41C>G (n.641-41C>G) c.899-41C>G (n.899-41C>G) c.782+532C>G (n.782+532C>G) c.803-41C>G (n.803-41C>G) c.443-41C>G (n.443-41C>G) c.887-41C>G (n.887-41C>G)	dbSNP
17	g.7673649G>T	CA656753442	TP53	c.920-41C>A (n.920-41C>A) c.524-41C>A (n.524-41C>A) c.641-41C>A (n.641-41C>A) c.899-41C>A (n.899-41C>A) c.782+532C>A (n.782+532C>A) c.803-41C>A (n.803-41C>A) c.443-41C>A (n.443-41C>A) c.887-41C>A (n.887-41C>A)	dbSNP COSMIC
17	g.7673650G>A	CA2733129884	TP53	c.920-42C>T (n.920-42C>T) c.524-42C>T (n.524-42C>T) c.641-42C>T (n.641-42C>T) c.899-42C>T (n.899-42C>T) c.782+531C>T (n.782+531C>T) c.803-42C>T (n.803-42C>T) c.443-42C>T (n.443-42C>T) c.887-42C>T (n.887-42C>T)	dbSNP
17	g.7673650G>C	CA2733129891	TP53	c.920-42C>G (n.920-42C>G) c.524-42C>G (n.524-42C>G) c.641-42C>G (n.641-42C>G) c.899-42C>G (n.899-42C>G) c.782+531C>G (n.782+531C>G) c.803-42C>G (n.803-42C>G) c.443-42C>G (n.443-42C>G) c.887-42C>G (n.887-42C>G)	dbSNP
17	g.7673650G>T	CA2733129892	TP53	c.920-42C>A (n.920-42C>A) c.524-42C>A (n.524-42C>A) c.641-42C>A (n.641-42C>A) c.899-42C>A (n.899-42C>A) c.782+531C>A (n.782+531C>A) c.803-42C>A (n.803-42C>A) c.443-42C>A (n.443-42C>A) c.887-42C>A (n.887-42C>A)	dbSNP
17	g.7673651C>A	CA2733129897	TP53	c.920-43G>T (n.920-43G>T) c.524-43G>T (n.524-43G>T) c.641-43G>T (n.641-43G>T) c.899-43G>T (n.899-43G>T) c.782+530G>T (n.782+530G>T) c.803-43G>T (n.803-43G>T) c.443-43G>T (n.443-43G>T) c.887-43G>T (n.887-43G>T)	dbSNP
17	g.7673651C>G	CA2733129896	TP53	c.920-43G>C (n.920-43G>C) c.524-43G>C (n.524-43G>C) c.641-43G>C (n.641-43G>C) c.899-43G>C (n.899-43G>C) c.782+530G>C (n.782+530G>C) c.803-43G>C (n.803-43G>C) c.443-43G>C (n.443-43G>C) c.887-43G>C (n.887-43G>C)	dbSNP
17	g.7673651C>T	CA2733129895	TP53	c.920-43G>A (n.920-43G>A) c.524-43G>A (n.524-43G>A) c.641-43G>A (n.641-43G>A) c.899-43G>A (n.899-43G>A) c.782+530G>A (n.782+530G>A) c.803-43G>A (n.803-43G>A) c.443-43G>A (n.443-43G>A) c.887-43G>A (n.887-43G>A)	dbSNP
17	g.7673652A=	CA2245948181	TP53	c.920-44T= (n.920-44T=) c.524-44T= (n.524-44T=) c.641-44T= (n.641-44T=) c.899-44T= (n.899-44T=) c.782+529T= (n.782+529T=) c.803-44T= (n.803-44T=) c.443-44T= (n.443-44T=) c.887-44T= (n.887-44T=)
17	g.7673652A>C	CA2732985615	TP53	c.920-44T>G (n.920-44T>G) c.524-44T>G (n.524-44T>G) c.641-44T>G (n.641-44T>G) c.899-44T>G (n.899-44T>G) c.782+529T>G (n.782+529T>G) c.803-44T>G (n.803-44T>G) c.443-44T>G (n.443-44T>G) c.887-44T>G (n.887-44T>G)	dbSNP
17	g.7673652A>G	CA2245948184	TP53	c.920-44T>C (n.920-44T>C) c.524-44T>C (n.524-44T>C) c.641-44T>C (n.641-44T>C) c.899-44T>C (n.899-44T>C) c.782+529T>C (n.782+529T>C) c.803-44T>C (n.803-44T>C) c.443-44T>C (n.443-44T>C) c.887-44T>C (n.887-44T>C)	dbSNP gnomAD v4
17	g.7673652A>T	CA2732985616	TP53	c.920-44T>A (n.920-44T>A) c.524-44T>A (n.524-44T>A) c.641-44T>A (n.641-44T>A) c.899-44T>A (n.899-44T>A) c.782+529T>A (n.782+529T>A) c.803-44T>A (n.803-44T>A) c.443-44T>A (n.443-44T>A) c.887-44T>A (n.887-44T>A)	dbSNP
17	g.7673654A>C	CA2635874468	TP53	c.920-46T>G (n.920-46T>G) c.524-46T>G (n.524-46T>G) c.641-46T>G (n.641-46T>G) c.899-46T>G (n.899-46T>G) c.782+527T>G (n.782+527T>G) c.803-46T>G (n.803-46T>G) c.443-46T>G (n.443-46T>G) c.887-46T>G (n.887-46T>G)	gnomAD v4
17	g.7673654A>G	CA2733129899	TP53	c.920-46T>C (n.920-46T>C) c.524-46T>C (n.524-46T>C) c.641-46T>C (n.641-46T>C) c.899-46T>C (n.899-46T>C) c.782+527T>C (n.782+527T>C) c.803-46T>C (n.803-46T>C) c.443-46T>C (n.443-46T>C) c.887-46T>C (n.887-46T>C)	dbSNP
17	g.7673654A>T	CA2733129898	TP53	c.920-46T>A (n.920-46T>A) c.524-46T>A (n.524-46T>A) c.641-46T>A (n.641-46T>A) c.899-46T>A (n.899-46T>A) c.782+527T>A (n.782+527T>A) c.803-46T>A (n.803-46T>A) c.443-46T>A (n.443-46T>A) c.887-46T>A (n.887-46T>A)	dbSNP
17	g.7673655A=	CA2245948192	TP53	c.920-47T= (n.920-47T=) c.524-47T= (n.524-47T=) c.641-47T= (n.641-47T=) c.899-47T= (n.899-47T=) c.782+526T= (n.782+526T=) c.803-47T= (n.803-47T=) c.443-47T= (n.443-47T=) c.887-47T= (n.887-47T=)
17	g.7673655A>C	CA2732985618	TP53	c.920-47T>G (n.920-47T>G) c.524-47T>G (n.524-47T>G) c.641-47T>G (n.641-47T>G) c.899-47T>G (n.899-47T>G) c.782+526T>G (n.782+526T>G) c.803-47T>G (n.803-47T>G) c.443-47T>G (n.443-47T>G) c.887-47T>G (n.887-47T>G)	dbSNP
17	g.7673655A>G	CA2245948193	TP53	c.920-47T>C (n.920-47T>C) c.524-47T>C (n.524-47T>C) c.641-47T>C (n.641-47T>C) c.899-47T>C (n.899-47T>C) c.782+526T>C (n.782+526T>C) c.803-47T>C (n.803-47T>C) c.443-47T>C (n.443-47T>C) c.887-47T>C (n.887-47T>C)	dbSNP
17	g.7673655A>T	CA2732985617	TP53	c.920-47T>A (n.920-47T>A) c.524-47T>A (n.524-47T>A) c.641-47T>A (n.641-47T>A) c.899-47T>A (n.899-47T>A) c.782+526T>A (n.782+526T>A) c.803-47T>A (n.803-47T>A) c.443-47T>A (n.443-47T>A) c.887-47T>A (n.887-47T>A)	dbSNP
17	g.7673656C>G	CA2635874469	TP53	c.919+45G>C (n.919+45G>C) c.523+45G>C (n.523+45G>C) c.640+45G>C (n.640+45G>C) c.898+45G>C (n.898+45G>C) c.782+525G>C (n.782+525G>C) c.802+45G>C (n.802+45G>C) c.442+45G>C (n.442+45G>C) c.886+45G>C (n.886+45G>C)	dbSNP gnomAD v4
17	g.7673656C>T	CA2635874470	TP53	c.919+45G>A (n.919+45G>A) c.523+45G>A (n.523+45G>A) c.640+45G>A (n.640+45G>A) c.898+45G>A (n.898+45G>A) c.782+525G>A (n.782+525G>A) c.802+45G>A (n.802+45G>A) c.442+45G>A (n.442+45G>A) c.886+45G>A (n.886+45G>A)	dbSNP gnomAD v4
17	g.7673657T>A	CA001284	TP53	c.919+44A>T (n.919+44A>T) c.523+44A>T (n.523+44A>T) c.640+44A>T (n.640+44A>T) c.898+44A>T (n.898+44A>T) c.782+524A>T (n.782+524A>T) c.802+44A>T (n.802+44A>T) c.442+44A>T (n.442+44A>T) c.886+44A>T (n.886+44A>T)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673657T>C	CA001286	TP53	c.919+44A>G (n.919+44A>G) c.523+44A>G (n.523+44A>G) c.640+44A>G (n.640+44A>G) c.898+44A>G (n.898+44A>G) c.782+524A>G (n.782+524A>G) c.802+44A>G (n.802+44A>G) c.442+44A>G (n.442+44A>G) c.886+44A>G (n.886+44A>G)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673657T=	CA2245948196	TP53	c.919+44A= (n.919+44A=) c.523+44A= (n.523+44A=) c.640+44A= (n.640+44A=) c.898+44A= (n.898+44A=) c.782+524A= (n.782+524A=) c.802+44A= (n.802+44A=) c.442+44A= (n.442+44A=) c.886+44A= (n.886+44A=)
17	g.7673658G>A	CA287486547	TP53	c.919+43C>T (n.919+43C>T) c.523+43C>T (n.523+43C>T) c.640+43C>T (n.640+43C>T) c.898+43C>T (n.898+43C>T) c.782+523C>T (n.782+523C>T) c.802+43C>T (n.802+43C>T) c.442+43C>T (n.442+43C>T) c.886+43C>T (n.886+43C>T)	dbSNP
17	g.7673658G>C	CA981209283	TP53	c.919+43C>G (n.919+43C>G) c.523+43C>G (n.523+43C>G) c.640+43C>G (n.640+43C>G) c.898+43C>G (n.898+43C>G) c.782+523C>G (n.782+523C>G) c.802+43C>G (n.802+43C>G) c.442+43C>G (n.442+43C>G) c.886+43C>G (n.886+43C>G)	dbSNP gnomAD v3 gnomAD v4
17	g.7673658G=	CA2245948202	TP53	c.919+43C= (n.919+43C=) c.523+43C= (n.523+43C=) c.640+43C= (n.640+43C=) c.898+43C= (n.898+43C=) c.782+523C= (n.782+523C=) c.802+43C= (n.802+43C=) c.442+43C= (n.442+43C=) c.886+43C= (n.886+43C=)
17	g.7673658G>T	CA2635874473	TP53	c.919+43C>A (n.919+43C>A) c.523+43C>A (n.523+43C>A) c.640+43C>A (n.640+43C>A) c.898+43C>A (n.898+43C>A) c.782+523C>A (n.782+523C>A) c.802+43C>A (n.802+43C>A) c.442+43C>A (n.442+43C>A) c.886+43C>A (n.886+43C>A)	gnomAD v4
17	g.7673659C>A	CA2733129902	TP53	c.919+42G>T (n.919+42G>T) c.523+42G>T (n.523+42G>T) c.640+42G>T (n.640+42G>T) c.898+42G>T (n.898+42G>T) c.782+522G>T (n.782+522G>T) c.802+42G>T (n.802+42G>T) c.442+42G>T (n.442+42G>T) c.886+42G>T (n.886+42G>T)	dbSNP
17	g.7673659C>G	CA2733130211	TP53	c.919+42G>C (n.919+42G>C) c.523+42G>C (n.523+42G>C) c.640+42G>C (n.640+42G>C) c.898+42G>C (n.898+42G>C) c.782+522G>C (n.782+522G>C) c.802+42G>C (n.802+42G>C) c.442+42G>C (n.442+42G>C) c.886+42G>C (n.886+42G>C)	dbSNP
17	g.7673659C>T	CA2635874476	TP53	c.919+42G>A (n.919+42G>A) c.523+42G>A (n.523+42G>A) c.640+42G>A (n.640+42G>A) c.898+42G>A (n.898+42G>A) c.782+522G>A (n.782+522G>A) c.802+42G>A (n.802+42G>A) c.442+42G>A (n.442+42G>A) c.886+42G>A (n.886+42G>A)	dbSNP gnomAD v4
17	g.7673660A>C	CA2576230618	TP53	c.919+41T>G (n.919+41T>G) c.523+41T>G (n.523+41T>G) c.640+41T>G (n.640+41T>G) c.898+41T>G (n.898+41T>G) c.782+521T>G (n.782+521T>G) c.802+41T>G (n.802+41T>G) c.442+41T>G (n.442+41T>G) c.886+41T>G (n.886+41T>G)	dbSNP
17	g.7673660A>G	CA2733130367	TP53	c.919+41T>C (n.919+41T>C) c.523+41T>C (n.523+41T>C) c.640+41T>C (n.640+41T>C) c.898+41T>C (n.898+41T>C) c.782+521T>C (n.782+521T>C) c.802+41T>C (n.802+41T>C) c.442+41T>C (n.442+41T>C) c.886+41T>C (n.886+41T>C)	dbSNP
17	g.7673660A>T	CA2733130214	TP53	c.919+41T>A (n.919+41T>A) c.523+41T>A (n.523+41T>A) c.640+41T>A (n.640+41T>A) c.898+41T>A (n.898+41T>A) c.782+521T>A (n.782+521T>A) c.802+41T>A (n.802+41T>A) c.442+41T>A (n.442+41T>A) c.886+41T>A (n.886+41T>A)	dbSNP
17	g.7673661C>A	CA2733130785	TP53	c.919+40G>T (n.919+40G>T) c.523+40G>T (n.523+40G>T) c.640+40G>T (n.640+40G>T) c.898+40G>T (n.898+40G>T) c.782+520G>T (n.782+520G>T) c.802+40G>T (n.802+40G>T) c.442+40G>T (n.442+40G>T) c.886+40G>T (n.886+40G>T)	dbSNP
17	g.7673661C>G	CA2733130786	TP53	c.919+40G>C (n.919+40G>C) c.523+40G>C (n.523+40G>C) c.640+40G>C (n.640+40G>C) c.898+40G>C (n.898+40G>C) c.782+520G>C (n.782+520G>C) c.802+40G>C (n.802+40G>C) c.442+40G>C (n.442+40G>C) c.886+40G>C (n.886+40G>C)	dbSNP
17	g.7673661C>T	CA2733130784	TP53	c.919+40G>A (n.919+40G>A) c.523+40G>A (n.523+40G>A) c.640+40G>A (n.640+40G>A) c.898+40G>A (n.898+40G>A) c.782+520G>A (n.782+520G>A) c.802+40G>A (n.802+40G>A) c.442+40G>A (n.442+40G>A) c.886+40G>A (n.886+40G>A)	dbSNP
17	g.7673662_7673663dup	CA2576230619	TP53	c.919+39_919+40dup (n.919+39_919+40dup) c.523+39_523+40dup (n.523+39_523+40dup) c.640+39_640+40dup (n.640+39_640+40dup) c.898+39_898+40dup (n.898+39_898+40dup) c.782+519_782+520dup (n.782+519_782+520dup) c.802+39_802+40dup (n.802+39_802+40dup) c.442+39_442+40dup (n.442+39_442+40dup) c.886+39_886+40dup (n.886+39_886+40dup)
17	g.7673663del	CA645587397	TP53	c.919+40del (n.919+40del) c.523+40del (n.523+40del) c.640+40del (n.640+40del) c.898+40del (n.898+40del) c.782+520del (n.782+520del) c.802+40del (n.802+40del) c.442+40del (n.442+40del) c.886+40del (n.886+40del)	COSMIC
17	g.7673662C>A	CA2733130787	TP53	c.919+39G>T (n.919+39G>T) c.523+39G>T (n.523+39G>T) c.640+39G>T (n.640+39G>T) c.898+39G>T (n.898+39G>T) c.782+519G>T (n.782+519G>T) c.802+39G>T (n.802+39G>T) c.442+39G>T (n.442+39G>T) c.886+39G>T (n.886+39G>T)	dbSNP
17	g.7673662C>G	CA2635874478	TP53	c.919+39G>C (n.919+39G>C) c.523+39G>C (n.523+39G>C) c.640+39G>C (n.640+39G>C) c.898+39G>C (n.898+39G>C) c.782+519G>C (n.782+519G>C) c.802+39G>C (n.802+39G>C) c.442+39G>C (n.442+39G>C) c.886+39G>C (n.886+39G>C)	dbSNP gnomAD v4
17	g.7673662C>T	CA2733130788	TP53	c.919+39G>A (n.919+39G>A) c.523+39G>A (n.523+39G>A) c.640+39G>A (n.640+39G>A) c.898+39G>A (n.898+39G>A) c.782+519G>A (n.782+519G>A) c.802+39G>A (n.802+39G>A) c.442+39G>A (n.442+39G>A) c.886+39G>A (n.886+39G>A)	dbSNP
17	g.7673663C>A	CA2732929153	TP53	c.919+38G>T (n.919+38G>T) c.523+38G>T (n.523+38G>T) c.640+38G>T (n.640+38G>T) c.898+38G>T (n.898+38G>T) c.782+518G>T (n.782+518G>T) c.802+38G>T (n.802+38G>T) c.442+38G>T (n.442+38G>T) c.886+38G>T (n.886+38G>T)	dbSNP
17	g.7673663C=	CA2245948205	TP53	c.919+38G= (n.919+38G=) c.523+38G= (n.523+38G=) c.640+38G= (n.640+38G=) c.898+38G= (n.898+38G=) c.782+518G= (n.782+518G=) c.802+38G= (n.802+38G=) c.442+38G= (n.442+38G=) c.886+38G= (n.886+38G=)
17	g.7673663C>G	CA001297	TP53	c.919+38G>C (n.919+38G>C) c.523+38G>C (n.523+38G>C) c.640+38G>C (n.640+38G>C) c.898+38G>C (n.898+38G>C) c.782+518G>C (n.782+518G>C) c.802+38G>C (n.802+38G>C) c.442+38G>C (n.442+38G>C) c.886+38G>C (n.886+38G>C)	dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673663C>T	CA2635874484	TP53	c.919+38G>A (n.919+38G>A) c.523+38G>A (n.523+38G>A) c.640+38G>A (n.640+38G>A) c.898+38G>A (n.898+38G>A) c.782+518G>A (n.782+518G>A) c.802+38G>A (n.802+38G>A) c.442+38G>A (n.442+38G>A) c.886+38G>A (n.886+38G>A)	dbSNP gnomAD v4
17	g.7673664T>C	CA2576230620	TP53	c.919+37A>G (n.919+37A>G) c.523+37A>G (n.523+37A>G) c.640+37A>G (n.640+37A>G) c.898+37A>G (n.898+37A>G) c.782+517A>G (n.782+517A>G) c.802+37A>G (n.802+37A>G) c.442+37A>G (n.442+37A>G) c.886+37A>G (n.886+37A>G)
17	g.7673665T>C	CA624865106	TP53	c.919+36A>G (n.919+36A>G) c.523+36A>G (n.523+36A>G) c.640+36A>G (n.640+36A>G) c.898+36A>G (n.898+36A>G) c.782+516A>G (n.782+516A>G) c.802+36A>G (n.802+36A>G) c.442+36A>G (n.442+36A>G) c.886+36A>G (n.886+36A>G)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673665T=	CA2245948211	TP53	c.919+36A= (n.919+36A=) c.523+36A= (n.523+36A=) c.640+36A= (n.640+36A=) c.898+36A= (n.898+36A=) c.782+516A= (n.782+516A=) c.802+36A= (n.802+36A=) c.442+36A= (n.442+36A=) c.886+36A= (n.886+36A=)
17	g.7673666G>A	CA2733130794	TP53	c.919+35C>T (n.919+35C>T) c.523+35C>T (n.523+35C>T) c.640+35C>T (n.640+35C>T) c.898+35C>T (n.898+35C>T) c.782+515C>T (n.782+515C>T) c.802+35C>T (n.802+35C>T) c.442+35C>T (n.442+35C>T) c.886+35C>T (n.886+35C>T)	dbSNP
17	g.7673666G>C	CA2733130793	TP53	c.919+35C>G (n.919+35C>G) c.523+35C>G (n.523+35C>G) c.640+35C>G (n.640+35C>G) c.898+35C>G (n.898+35C>G) c.782+515C>G (n.782+515C>G) c.802+35C>G (n.802+35C>G) c.442+35C>G (n.442+35C>G) c.886+35C>G (n.886+35C>G)	dbSNP
17	g.7673666G>T	CA2733130790	TP53	c.919+35C>A (n.919+35C>A) c.523+35C>A (n.523+35C>A) c.640+35C>A (n.640+35C>A) c.898+35C>A (n.898+35C>A) c.782+515C>A (n.782+515C>A) c.802+35C>A (n.802+35C>A) c.442+35C>A (n.442+35C>A) c.886+35C>A (n.886+35C>A)	dbSNP
17	g.7673667dup	CA2635874489	TP53	c.919+35dup (n.919+35dup) c.523+35dup (n.523+35dup) c.640+35dup (n.640+35dup) c.898+35dup (n.898+35dup) c.782+515dup (n.782+515dup) c.802+35dup (n.802+35dup) c.442+35dup (n.442+35dup) c.886+35dup (n.886+35dup)	gnomAD v4
17	g.7673667G>A	CA624865107	TP53	c.919+34C>T (n.919+34C>T) c.523+34C>T (n.523+34C>T) c.640+34C>T (n.640+34C>T) c.898+34C>T (n.898+34C>T) c.782+514C>T (n.782+514C>T) c.802+34C>T (n.802+34C>T) c.442+34C>T (n.442+34C>T) c.886+34C>T (n.886+34C>T)	dbSNP gnomAD v2 gnomAD v4 COSMIC
17	g.7673667G>C	CA2635874499	TP53	c.919+34C>G (n.919+34C>G) c.523+34C>G (n.523+34C>G) c.640+34C>G (n.640+34C>G) c.898+34C>G (n.898+34C>G) c.782+514C>G (n.782+514C>G) c.802+34C>G (n.802+34C>G) c.442+34C>G (n.442+34C>G) c.886+34C>G (n.886+34C>G)	dbSNP gnomAD v4
17	g.7673667G=	CA2245948216	TP53	c.919+34C= (n.919+34C=) c.523+34C= (n.523+34C=) c.640+34C= (n.640+34C=) c.898+34C= (n.898+34C=) c.782+514C= (n.782+514C=) c.802+34C= (n.802+34C=) c.442+34C= (n.442+34C=) c.886+34C= (n.886+34C=)
17	g.7673667G>T	CA2635874500	TP53	c.919+34C>A (n.919+34C>A) c.523+34C>A (n.523+34C>A) c.640+34C>A (n.640+34C>A) c.898+34C>A (n.898+34C>A) c.782+514C>A (n.782+514C>A) c.802+34C>A (n.802+34C>A) c.442+34C>A (n.442+34C>A) c.886+34C>A (n.886+34C>A)	dbSNP gnomAD v4
17	g.7673668T>A	CA2733130961	TP53	c.919+33A>T (n.919+33A>T) c.523+33A>T (n.523+33A>T) c.640+33A>T (n.640+33A>T) c.898+33A>T (n.898+33A>T) c.782+513A>T (n.782+513A>T) c.802+33A>T (n.802+33A>T) c.442+33A>T (n.442+33A>T) c.886+33A>T (n.886+33A>T)	dbSNP
17	g.7673668T>C	CA2733130970	TP53	c.919+33A>G (n.919+33A>G) c.523+33A>G (n.523+33A>G) c.640+33A>G (n.640+33A>G) c.898+33A>G (n.898+33A>G) c.782+513A>G (n.782+513A>G) c.802+33A>G (n.802+33A>G) c.442+33A>G (n.442+33A>G) c.886+33A>G (n.886+33A>G)	dbSNP
17	g.7673669C>A	CA645587398	TP53	c.919+32G>T (n.919+32G>T) c.523+32G>T (n.523+32G>T) c.640+32G>T (n.640+32G>T) c.898+32G>T (n.898+32G>T) c.782+512G>T (n.782+512G>T) c.802+32G>T (n.802+32G>T) c.442+32G>T (n.442+32G>T) c.886+32G>T (n.886+32G>T)	COSMIC
17	g.7673669C=	CA2245948221	TP53	c.919+32G= (n.919+32G=) c.523+32G= (n.523+32G=) c.640+32G= (n.640+32G=) c.898+32G= (n.898+32G=) c.782+512G= (n.782+512G=) c.802+32G= (n.802+32G=) c.442+32G= (n.442+32G=) c.886+32G= (n.886+32G=)
17	g.7673669C>G	CA2732952098	TP53	c.919+32G>C (n.919+32G>C) c.523+32G>C (n.523+32G>C) c.640+32G>C (n.640+32G>C) c.898+32G>C (n.898+32G>C) c.782+512G>C (n.782+512G>C) c.802+32G>C (n.802+32G>C) c.442+32G>C (n.442+32G>C) c.886+32G>C (n.886+32G>C)	dbSNP
17	g.7673669C>T	CA624865108	TP53	c.919+32G>A (n.919+32G>A) c.523+32G>A (n.523+32G>A) c.640+32G>A (n.640+32G>A) c.898+32G>A (n.898+32G>A) c.782+512G>A (n.782+512G>A) c.802+32G>A (n.802+32G>A) c.442+32G>A (n.442+32G>A) c.886+32G>A (n.886+32G>A)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673673_7673675del	CA2635874502	TP53	c.919+30_919+32del (n.919+30_919+32del) c.523+30_523+32del (n.523+30_523+32del) c.640+30_640+32del (n.640+30_640+32del) c.898+30_898+32del (n.898+30_898+32del) c.782+510_782+512del (n.782+510_782+512del) c.802+30_802+32del (n.802+30_802+32del) c.442+30_442+32del (n.442+30_442+32del) c.886+30_886+32del (n.886+30_886+32del)	gnomAD v4
17	g.7673670T>A	CA2732929847	TP53	c.919+31A>T (n.919+31A>T) c.523+31A>T (n.523+31A>T) c.640+31A>T (n.640+31A>T) c.898+31A>T (n.898+31A>T) c.782+511A>T (n.782+511A>T) c.802+31A>T (n.802+31A>T) c.442+31A>T (n.442+31A>T) c.886+31A>T (n.886+31A>T)	dbSNP
17	g.7673670T>C	CA287486550	TP53	c.919+31A>G (n.919+31A>G) c.523+31A>G (n.523+31A>G) c.640+31A>G (n.640+31A>G) c.898+31A>G (n.898+31A>G) c.782+511A>G (n.782+511A>G) c.802+31A>G (n.802+31A>G) c.442+31A>G (n.442+31A>G) c.886+31A>G (n.886+31A>G)	dbSNP
17	g.7673670T=	CA2245948228	TP53	c.919+31A= (n.919+31A=) c.523+31A= (n.523+31A=) c.640+31A= (n.640+31A=) c.898+31A= (n.898+31A=) c.782+511A= (n.782+511A=) c.802+31A= (n.802+31A=) c.442+31A= (n.442+31A=) c.886+31A= (n.886+31A=)
17	g.7673671_7673672dup	CA8354860	TP53	c.919+29_919+30dup (n.919+29_919+30dup) c.523+29_523+30dup (n.523+29_523+30dup) c.640+29_640+30dup (n.640+29_640+30dup) c.898+29_898+30dup (n.898+29_898+30dup) c.782+509_782+510dup (n.782+509_782+510dup) c.802+29_802+30dup (n.802+29_802+30dup) c.442+29_442+30dup (n.442+29_442+30dup) c.886+29_886+30dup (n.886+29_886+30dup)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673672C>A	CA2732985620	TP53	c.919+29G>T (n.919+29G>T) c.523+29G>T (n.523+29G>T) c.640+29G>T (n.640+29G>T) c.898+29G>T (n.898+29G>T) c.782+509G>T (n.782+509G>T) c.802+29G>T (n.802+29G>T) c.442+29G>T (n.442+29G>T) c.886+29G>T (n.886+29G>T)	dbSNP
17	g.7673672C=	CA2245948234	TP53	c.919+29G= (n.919+29G=) c.523+29G= (n.523+29G=) c.640+29G= (n.640+29G=) c.898+29G= (n.898+29G=) c.782+509G= (n.782+509G=) c.802+29G= (n.802+29G=) c.442+29G= (n.442+29G=) c.886+29G= (n.886+29G=)
17	g.7673672C>G	CA2732985619	TP53	c.919+29G>C (n.919+29G>C) c.523+29G>C (n.523+29G>C) c.640+29G>C (n.640+29G>C) c.898+29G>C (n.898+29G>C) c.782+509G>C (n.782+509G>C) c.802+29G>C (n.802+29G>C) c.442+29G>C (n.442+29G>C) c.886+29G>C (n.886+29G>C)	dbSNP
17	g.7673672C>T	CA2245948237	TP53	c.919+29G>A (n.919+29G>A) c.523+29G>A (n.523+29G>A) c.640+29G>A (n.640+29G>A) c.898+29G>A (n.898+29G>A) c.782+509G>A (n.782+509G>A) c.802+29G>A (n.802+29G>A) c.442+29G>A (n.442+29G>A) c.886+29G>A (n.886+29G>A)	dbSNP gnomAD v4
17	g.7673674C>G	CA645587399	TP53	c.919+27G>C (n.919+27G>C) c.523+27G>C (n.523+27G>C) c.640+27G>C (n.640+27G>C) c.898+27G>C (n.898+27G>C) c.782+507G>C (n.782+507G>C) c.802+27G>C (n.802+27G>C) c.442+27G>C (n.442+27G>C) c.886+27G>C (n.886+27G>C)	COSMIC
17	g.7673675del	CA2635874503	TP53	c.919+27del (n.919+27del) c.523+27del (n.523+27del) c.640+27del (n.640+27del) c.898+27del (n.898+27del) c.782+507del (n.782+507del) c.802+27del (n.802+27del) c.442+27del (n.442+27del) c.886+27del (n.886+27del)	gnomAD v4
17	g.7673675C=	CA2245948243	TP53	c.919+26G= (n.919+26G=) c.523+26G= (n.523+26G=) c.640+26G= (n.640+26G=) c.898+26G= (n.898+26G=) c.782+506G= (n.782+506G=) c.802+26G= (n.802+26G=) c.442+26G= (n.442+26G=) c.886+26G= (n.886+26G=)
17	g.7673675C>G	CA2732930575	TP53	c.919+26G>C (n.919+26G>C) c.523+26G>C (n.523+26G>C) c.640+26G>C (n.640+26G>C) c.898+26G>C (n.898+26G>C) c.782+506G>C (n.782+506G>C) c.802+26G>C (n.802+26G>C) c.442+26G>C (n.442+26G>C) c.886+26G>C (n.886+26G>C)	dbSNP
17	g.7673675C>T	CA001305	TP53	c.919+26G>A (n.919+26G>A) c.523+26G>A (n.523+26G>A) c.640+26G>A (n.640+26G>A) c.898+26G>A (n.898+26G>A) c.782+506G>A (n.782+506G>A) c.802+26G>A (n.802+26G>A) c.442+26G>A (n.442+26G>A) c.886+26G>A (n.886+26G>A)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673675delinsAT	CA645587400	TP53	c.919+26delinsAT (n.919+26delinsAT) c.523+26delinsAT (n.523+26delinsAT) c.640+26delinsAT (n.640+26delinsAT) c.898+26delinsAT (n.898+26delinsAT) c.782+506delinsAT (n.782+506delinsAT) c.802+26delinsAT (n.802+26delinsAT) c.442+26delinsAT (n.442+26delinsAT) c.886+26delinsAT (n.886+26delinsAT)	COSMIC
17	g.7673676A>C	CA2733131258	TP53	c.919+25T>G (n.919+25T>G) c.523+25T>G (n.523+25T>G) c.640+25T>G (n.640+25T>G) c.898+25T>G (n.898+25T>G) c.782+505T>G (n.782+505T>G) c.802+25T>G (n.802+25T>G) c.442+25T>G (n.442+25T>G) c.886+25T>G (n.886+25T>G)	dbSNP
17	g.7673676A>G	CA2733131228	TP53	c.919+25T>C (n.919+25T>C) c.523+25T>C (n.523+25T>C) c.640+25T>C (n.640+25T>C) c.898+25T>C (n.898+25T>C) c.782+505T>C (n.782+505T>C) c.802+25T>C (n.802+25T>C) c.442+25T>C (n.442+25T>C) c.886+25T>C (n.886+25T>C)	dbSNP
17	g.7673676A>T	CA2733131215	TP53	c.919+25T>A (n.919+25T>A) c.523+25T>A (n.523+25T>A) c.640+25T>A (n.640+25T>A) c.898+25T>A (n.898+25T>A) c.782+505T>A (n.782+505T>A) c.802+25T>A (n.802+25T>A) c.442+25T>A (n.442+25T>A) c.886+25T>A (n.886+25T>A)	dbSNP
17	g.7673677C>A	CA2635874507	TP53	c.919+24G>T (n.919+24G>T) c.523+24G>T (n.523+24G>T) c.640+24G>T (n.640+24G>T) c.898+24G>T (n.898+24G>T) c.782+504G>T (n.782+504G>T) c.802+24G>T (n.802+24G>T) c.442+24G>T (n.442+24G>T) c.886+24G>T (n.886+24G>T)	gnomAD v4
17	g.7673677C>G	CA2733131262	TP53	c.919+24G>C (n.919+24G>C) c.523+24G>C (n.523+24G>C) c.640+24G>C (n.640+24G>C) c.898+24G>C (n.898+24G>C) c.782+504G>C (n.782+504G>C) c.802+24G>C (n.802+24G>C) c.442+24G>C (n.442+24G>C) c.886+24G>C (n.886+24G>C)	dbSNP
17	g.7673677C>T	CA645587401	TP53	c.919+24G>A (n.919+24G>A) c.523+24G>A (n.523+24G>A) c.640+24G>A (n.640+24G>A) c.898+24G>A (n.898+24G>A) c.782+504G>A (n.782+504G>A) c.802+24G>A (n.802+24G>A) c.442+24G>A (n.442+24G>A) c.886+24G>A (n.886+24G>A)	dbSNP COSMIC
17	g.7673678C>A	CA2635874509	TP53	c.919+23G>T (n.919+23G>T) c.523+23G>T (n.523+23G>T) c.640+23G>T (n.640+23G>T) c.898+23G>T (n.898+23G>T) c.782+503G>T (n.782+503G>T) c.802+23G>T (n.802+23G>T) c.442+23G>T (n.442+23G>T) c.886+23G>T (n.886+23G>T)	dbSNP gnomAD v4
17	g.7673678C=	CA2245948246	TP53	c.919+23G= (n.919+23G=) c.523+23G= (n.523+23G=) c.640+23G= (n.640+23G=) c.898+23G= (n.898+23G=) c.782+503G= (n.782+503G=) c.802+23G= (n.802+23G=) c.442+23G= (n.442+23G=) c.886+23G= (n.886+23G=)
17	g.7673678C>G	CA2635874510	TP53	c.919+23G>C (n.919+23G>C) c.523+23G>C (n.523+23G>C) c.640+23G>C (n.640+23G>C) c.898+23G>C (n.898+23G>C) c.782+503G>C (n.782+503G>C) c.802+23G>C (n.802+23G>C) c.442+23G>C (n.442+23G>C) c.886+23G>C (n.886+23G>C)	dbSNP gnomAD v4
17	g.7673678C>T	CA001310	TP53	c.919+23G>A (n.919+23G>A) c.523+23G>A (n.523+23G>A) c.640+23G>A (n.640+23G>A) c.898+23G>A (n.898+23G>A) c.782+503G>A (n.782+503G>A) c.802+23G>A (n.802+23G>A) c.442+23G>A (n.442+23G>A) c.886+23G>A (n.886+23G>A)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673679G>A	CA001316	TP53	c.919+22C>T (n.919+22C>T) c.523+22C>T (n.523+22C>T) c.640+22C>T (n.640+22C>T) c.898+22C>T (n.898+22C>T) c.782+502C>T (n.782+502C>T) c.802+22C>T (n.802+22C>T) c.442+22C>T (n.442+22C>T) c.886+22C>T (n.886+22C>T)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673679G>C	CA2732927444	TP53	c.919+22C>G (n.919+22C>G) c.523+22C>G (n.523+22C>G) c.640+22C>G (n.640+22C>G) c.898+22C>G (n.898+22C>G) c.782+502C>G (n.782+502C>G) c.802+22C>G (n.802+22C>G) c.442+22C>G (n.442+22C>G) c.886+22C>G (n.886+22C>G)	dbSNP
17	g.7673679G=	CA2245948250	TP53	c.919+22C= (n.919+22C=) c.523+22C= (n.523+22C=) c.640+22C= (n.640+22C=) c.898+22C= (n.898+22C=) c.782+502C= (n.782+502C=) c.802+22C= (n.802+22C=) c.442+22C= (n.442+22C=) c.886+22C= (n.886+22C=)
17	g.7673679G>T	CA2732927443	TP53	c.919+22C>A (n.919+22C>A) c.523+22C>A (n.523+22C>A) c.640+22C>A (n.640+22C>A) c.898+22C>A (n.898+22C>A) c.782+502C>A (n.782+502C>A) c.802+22C>A (n.802+22C>A) c.442+22C>A (n.442+22C>A) c.886+22C>A (n.886+22C>A)	dbSNP
17	g.7673679_7673682delinsGCTT	CA2245948253	TP53	c.919+19_919+22delinsAAGC (n.919+19_919+22delinsAAGC) c.523+19_523+22delinsAAGC (n.523+19_523+22delinsAAGC) c.640+19_640+22delinsAAGC (n.640+19_640+22delinsAAGC) c.898+19_898+22delinsAAGC (n.898+19_898+22delinsAAGC) c.782+499_782+502delinsAAGC (n.782+499_782+502delinsAAGC) c.802+19_802+22delinsAAGC (n.802+19_802+22delinsAAGC) c.442+19_442+22delinsAAGC (n.442+19_442+22delinsAAGC) c.886+19_886+22delinsAAGC (n.886+19_886+22delinsAAGC)
17	g.7673683_7673694del	CA2739265582	TP53	c.919+11_919+22del (n.919+11_919+22del) c.523+11_523+22del (n.523+11_523+22del) c.640+11_640+22del (n.640+11_640+22del) c.898+11_898+22del (n.898+11_898+22del) c.782+491_782+502del (n.782+491_782+502del) c.802+11_802+22del (n.802+11_802+22del) c.442+11_442+22del (n.442+11_442+22del) c.886+11_886+22del (n.886+11_886+22del)	ClinVar
17	g.7673680C>A	CA2733131410	TP53	c.919+21G>T (n.919+21G>T) c.523+21G>T (n.523+21G>T) c.640+21G>T (n.640+21G>T) c.898+21G>T (n.898+21G>T) c.782+501G>T (n.782+501G>T) c.802+21G>T (n.802+21G>T) c.442+21G>T (n.442+21G>T) c.886+21G>T (n.886+21G>T)	dbSNP
17	g.7673680C>G	CA2733131355	TP53	c.919+21G>C (n.919+21G>C) c.523+21G>C (n.523+21G>C) c.640+21G>C (n.640+21G>C) c.898+21G>C (n.898+21G>C) c.782+501G>C (n.782+501G>C) c.802+21G>C (n.802+21G>C) c.442+21G>C (n.442+21G>C) c.886+21G>C (n.886+21G>C)	dbSNP
17	g.7673680C>T	CA2733131354	TP53	c.919+21G>A (n.919+21G>A) c.523+21G>A (n.523+21G>A) c.640+21G>A (n.640+21G>A) c.898+21G>A (n.898+21G>A) c.782+501G>A (n.782+501G>A) c.802+21G>A (n.802+21G>A) c.442+21G>A (n.442+21G>A) c.886+21G>A (n.886+21G>A)	dbSNP
17	g.7673683_7673685del	CA16620614	TP53	c.919+19_919+21del (n.919+19_919+21del) c.523+19_523+21del (n.523+19_523+21del) c.640+19_640+21del (n.640+19_640+21del) c.898+19_898+21del (n.898+19_898+21del) c.782+499_782+501del (n.782+499_782+501del) c.802+19_802+21del (n.802+19_802+21del) c.442+19_442+21del (n.442+19_442+21del) c.886+19_886+21del (n.886+19_886+21del)	ClinVar dbSNP gnomAD v4
17	g.7673681T>A	CA2245948260	TP53	c.919+20A>T (n.919+20A>T) c.523+20A>T (n.523+20A>T) c.640+20A>T (n.640+20A>T) c.898+20A>T (n.898+20A>T) c.782+500A>T (n.782+500A>T) c.802+20A>T (n.802+20A>T) c.442+20A>T (n.442+20A>T) c.886+20A>T (n.886+20A>T)	dbSNP
17	g.7673681T>C	CA2573154632	TP53	c.919+20A>G (n.919+20A>G) c.523+20A>G (n.523+20A>G) c.640+20A>G (n.640+20A>G) c.898+20A>G (n.898+20A>G) c.782+500A>G (n.782+500A>G) c.802+20A>G (n.802+20A>G) c.442+20A>G (n.442+20A>G) c.886+20A>G (n.886+20A>G)	ClinVar dbSNP
17	g.7673681T>G	CA2635874518	TP53	c.919+20A>C (n.919+20A>C) c.523+20A>C (n.523+20A>C) c.640+20A>C (n.640+20A>C) c.898+20A>C (n.898+20A>C) c.782+500A>C (n.782+500A>C) c.802+20A>C (n.802+20A>C) c.442+20A>C (n.442+20A>C) c.886+20A>C (n.886+20A>C)	gnomAD v4
17	g.7673681T=	CA2245948259	TP53	c.919+20A= (n.919+20A=) c.523+20A= (n.523+20A=) c.640+20A= (n.640+20A=) c.898+20A= (n.898+20A=) c.782+500A= (n.782+500A=) c.802+20A= (n.802+20A=) c.442+20A= (n.442+20A=) c.886+20A= (n.886+20A=)
17	g.7673682T>A	CA2733131742	TP53	c.919+19A>T (n.919+19A>T) c.523+19A>T (n.523+19A>T) c.640+19A>T (n.640+19A>T) c.898+19A>T (n.898+19A>T) c.782+499A>T (n.782+499A>T) c.802+19A>T (n.802+19A>T) c.442+19A>T (n.442+19A>T) c.886+19A>T (n.886+19A>T)	dbSNP
17	g.7673682T>C	CA2576230621	TP53	c.919+19A>G (n.919+19A>G) c.523+19A>G (n.523+19A>G) c.640+19A>G (n.640+19A>G) c.898+19A>G (n.898+19A>G) c.782+499A>G (n.782+499A>G) c.802+19A>G (n.802+19A>G) c.442+19A>G (n.442+19A>G) c.886+19A>G (n.886+19A>G)	dbSNP
17	g.7673682T>G	CA2733131674	TP53	c.919+19A>C (n.919+19A>C) c.523+19A>C (n.523+19A>C) c.640+19A>C (n.640+19A>C) c.898+19A>C (n.898+19A>C) c.782+499A>C (n.782+499A>C) c.802+19A>C (n.802+19A>C) c.442+19A>C (n.442+19A>C) c.886+19A>C (n.886+19A>C)	dbSNP
17	g.7673683C>A	CA2733131770	TP53	c.919+18G>T (n.919+18G>T) c.523+18G>T (n.523+18G>T) c.640+18G>T (n.640+18G>T) c.898+18G>T (n.898+18G>T) c.782+498G>T (n.782+498G>T) c.802+18G>T (n.802+18G>T) c.442+18G>T (n.442+18G>T) c.886+18G>T (n.886+18G>T)	dbSNP
17	g.7673683C>G	CA645587402	TP53	c.919+18G>C (n.919+18G>C) c.523+18G>C (n.523+18G>C) c.640+18G>C (n.640+18G>C) c.898+18G>C (n.898+18G>C) c.782+498G>C (n.782+498G>C) c.802+18G>C (n.802+18G>C) c.442+18G>C (n.442+18G>C) c.886+18G>C (n.886+18G>C)	dbSNP COSMIC
17	g.7673683C>T	CA2733131823	TP53	c.919+18G>A (n.919+18G>A) c.523+18G>A (n.523+18G>A) c.640+18G>A (n.640+18G>A) c.898+18G>A (n.898+18G>A) c.782+498G>A (n.782+498G>A) c.802+18G>A (n.802+18G>A) c.442+18G>A (n.442+18G>A) c.886+18G>A (n.886+18G>A)	dbSNP
17	g.7673684T>C	CA16608661	TP53	c.919+17A>G (n.919+17A>G) c.523+17A>G (n.523+17A>G) c.640+17A>G (n.640+17A>G) c.898+17A>G (n.898+17A>G) c.782+497A>G (n.782+497A>G) c.802+17A>G (n.802+17A>G) c.442+17A>G (n.442+17A>G) c.886+17A>G (n.886+17A>G)	ClinVar dbSNP gnomAD v4
17	g.7673684T=	CA2245948265	TP53	c.919+17A= (n.919+17A=) c.523+17A= (n.523+17A=) c.640+17A= (n.640+17A=) c.898+17A= (n.898+17A=) c.782+497A= (n.782+497A=) c.802+17A= (n.802+17A=) c.442+17A= (n.442+17A=) c.886+17A= (n.886+17A=)
17	g.7673684_7673686delinsGATGATTCTCTTCGATTCCATTCGATAATTCCGTTTGATTCCGTTAGATGTTGATTCCATTCGAGTCAATTCGATGATAATTCCATTCAATTCTATGCGATGATTCCATTCCATTCCATTTGAAGATGATTCCATTCGAGACCATTCGATGATTGCATTCAATTCATTCGATGACGATTCCATTCAATTCCGTTCAATGTTTCCATTAGATTCCATCTGATGATGATTCCATTCGATTCCATTTGATGATGATTCCATGCGATTCCATTAGATGATGACTCCTTTCATTTCCATTCGATGATGATTCCATTCGTTTCCA	CA2825002633	TP53	c.919+15_919+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.919+15_919+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.523+15_523+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.523+15_523+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.640+15_640+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.640+15_640+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.898+15_898+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.898+15_898+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.782+495_782+497delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.782+495_782+497delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.802+15_802+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.802+15_802+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.442+15_442+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.442+15_442+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.886+15_886+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.886+15_886+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCATGGAATCATCATCAAATGGAATCGAATGGAATCATCATCAGATGGAATCTAATGGAAACATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGAATGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATTGAATGGAATTATCATCGAATTGACTCGAATGGAATCAACATCTAACGGAATCAAACGGAATTATCGAATGGAATCGAAGAGAATCATC)	ClinVar
17	g.7673684_7673686delinsGATGATTCTCTTCGATTCCATTCGATAATTCCGTTTTTTTCCGTTTGATGTTGATTCCATTCGATTCCATTCGATGATAATTCCATTCGATTCTATGCGATGATTCCATTCCATTCCATTTGAAGATGATTCCATTCGAGACCATTCGATGATTGCAGTCAATTCATTCGATGACGATTCCATTCAATTCCGTTCAATGATTCCATTTGATTCCATTTGATGTTGATTCCATTCGATTCCATTTTATGATGATTCCATGCAATTCCATTAGATGATGACTCCTTTCATTTCCATTCGATGATGATTCCATTCGTTTCCA	CA2580094908	TP53	c.919+15_919+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.919+15_919+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.523+15_523+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.523+15_523+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.640+15_640+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.640+15_640+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.898+15_898+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.898+15_898+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.782+495_782+497delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.782+495_782+497delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.802+15_802+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.802+15_802+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.442+15_442+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.442+15_442+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC) c.886+15_886+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC (n.886+15_886+17delinsTGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATTGCATGGAATCATCATAAAATGGAATCGAATGGAATCAACATCAAATGGAATCAAATGGAATCATTGAACGGAATTGAATGGAATCGTCATCGAATGAATTGACTGCAATCATCGAATGGTCTCGAATGGAATCATCTTCAAATGGAATGGAATGGAATCATCGCATAGAATCGAATGGAATTATCATCGAATGGAATCGAATGGAATCAACATCAAACGGAAAAAAACGGAATTATCGAATGGAATCGAAGAGAATCATC)	ClinVar
17	g.7673685T>A	CA2733131832	TP53	c.919+16A>T (n.919+16A>T) c.523+16A>T (n.523+16A>T) c.640+16A>T (n.640+16A>T) c.898+16A>T (n.898+16A>T) c.782+496A>T (n.782+496A>T) c.802+16A>T (n.802+16A>T) c.442+16A>T (n.442+16A>T) c.886+16A>T (n.886+16A>T)	dbSNP
17	g.7673685T>C	CA2580094909	TP53	c.919+16A>G (n.919+16A>G) c.523+16A>G (n.523+16A>G) c.640+16A>G (n.640+16A>G) c.898+16A>G (n.898+16A>G) c.782+496A>G (n.782+496A>G) c.802+16A>G (n.802+16A>G) c.442+16A>G (n.442+16A>G) c.886+16A>G (n.886+16A>G)	ClinVar dbSNP
17	g.7673685_7673703delinsTGTCCTGCTTGCTTACCTC	CA2245948268	TP53	c.917_919+16delinsGAGGTAAGCAAGCAGGACA c.521_523+16delinsGAGGTAAGCAAGCAGGACA c.638_640+16delinsGAGGTAAGCAAGCAGGACA c.896_898+16delinsGAGGTAAGCAAGCAGGACA c.782+478_782+496delinsGAGGTAAGCAAGCAGGACA (n.782+478_782+496delinsGAGGTAAGCAAGCAGGACA) c.800_802+16delinsGAGGTAAGCAAGCAGGACA c.440_442+16delinsGAGGTAAGCAAGCAGGACA c.884_886+16delinsGAGGTAAGCAAGCAGGACA
17	g.7673686G>A	CA645587403	TP53	c.919+15C>T (n.919+15C>T) c.523+15C>T (n.523+15C>T) c.640+15C>T (n.640+15C>T) c.898+15C>T (n.898+15C>T) c.782+495C>T (n.782+495C>T) c.802+15C>T (n.802+15C>T) c.442+15C>T (n.442+15C>T) c.886+15C>T (n.886+15C>T)	ClinVar dbSNP COSMIC
17	g.7673686G>C	CA16608662	TP53	c.919+15C>G (n.919+15C>G) c.523+15C>G (n.523+15C>G) c.640+15C>G (n.640+15C>G) c.898+15C>G (n.898+15C>G) c.782+495C>G (n.782+495C>G) c.802+15C>G (n.802+15C>G) c.442+15C>G (n.442+15C>G) c.886+15C>G (n.886+15C>G)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673686G=	CA2245948275	TP53	c.919+15C= (n.919+15C=) c.523+15C= (n.523+15C=) c.640+15C= (n.640+15C=) c.898+15C= (n.898+15C=) c.782+495C= (n.782+495C=) c.802+15C= (n.802+15C=) c.442+15C= (n.442+15C=) c.886+15C= (n.886+15C=)
17	g.7673686G>T	CA2732943611	TP53	c.919+15C>A (n.919+15C>A) c.523+15C>A (n.523+15C>A) c.640+15C>A (n.640+15C>A) c.898+15C>A (n.898+15C>A) c.782+495C>A (n.782+495C>A) c.802+15C>A (n.802+15C>A) c.442+15C>A (n.442+15C>A) c.886+15C>A (n.886+15C>A)	dbSNP
17	g.7673687_7673704del	CA915949519	TP53	c.917_919+15del c.521_523+15del c.638_640+15del c.896_898+15del c.782+478_782+495del (n.782+478_782+495del) c.800_802+15del c.440_442+15del c.884_886+15del	ClinVar dbSNP
17	g.7673687T>G	CA2733131949	TP53	c.919+14A>C (n.919+14A>C) c.523+14A>C (n.523+14A>C) c.640+14A>C (n.640+14A>C) c.898+14A>C (n.898+14A>C) c.782+494A>C (n.782+494A>C) c.802+14A>C (n.802+14A>C) c.442+14A>C (n.442+14A>C) c.886+14A>C (n.886+14A>C)	dbSNP
17	g.7673687_7673688delinsTC	CA2245948281	TP53	c.919+13_919+14delinsGA (n.919+13_919+14delinsGA) c.523+13_523+14delinsGA (n.523+13_523+14delinsGA) c.640+13_640+14delinsGA (n.640+13_640+14delinsGA) c.898+13_898+14delinsGA (n.898+13_898+14delinsGA) c.782+493_782+494delinsGA (n.782+493_782+494delinsGA) c.802+13_802+14delinsGA (n.802+13_802+14delinsGA) c.442+13_442+14delinsGA (n.442+13_442+14delinsGA) c.886+13_886+14delinsGA (n.886+13_886+14delinsGA)
17	g.7673688C>A	CA001323	TP53	c.919+13G>T (n.919+13G>T) c.523+13G>T (n.523+13G>T) c.640+13G>T (n.640+13G>T) c.898+13G>T (n.898+13G>T) c.782+493G>T (n.782+493G>T) c.802+13G>T (n.802+13G>T) c.442+13G>T (n.442+13G>T) c.886+13G>T (n.886+13G>T)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673688C=	CA2245948283	TP53	c.919+13G= (n.919+13G=) c.523+13G= (n.523+13G=) c.640+13G= (n.640+13G=) c.898+13G= (n.898+13G=) c.782+493G= (n.782+493G=) c.802+13G= (n.802+13G=) c.442+13G= (n.442+13G=) c.886+13G= (n.886+13G=)
17	g.7673688C>G	CA2732930576	TP53	c.919+13G>C (n.919+13G>C) c.523+13G>C (n.523+13G>C) c.640+13G>C (n.640+13G>C) c.898+13G>C (n.898+13G>C) c.782+493G>C (n.782+493G>C) c.802+13G>C (n.802+13G>C) c.442+13G>C (n.442+13G>C) c.886+13G>C (n.886+13G>C)	dbSNP
17	g.7673688C>T	CA2573154633	TP53	c.919+13G>A (n.919+13G>A) c.523+13G>A (n.523+13G>A) c.640+13G>A (n.640+13G>A) c.898+13G>A (n.898+13G>A) c.782+493G>A (n.782+493G>A) c.802+13G>A (n.802+13G>A) c.442+13G>A (n.442+13G>A) c.886+13G>A (n.886+13G>A)	ClinVar dbSNP
17	g.7673689del	CA287486558	TP53	c.919+13del (n.919+13del) c.523+13del (n.523+13del) c.640+13del (n.640+13del) c.898+13del (n.898+13del) c.782+493del (n.782+493del) c.802+13del (n.802+13del) c.442+13del (n.442+13del) c.886+13del (n.886+13del)	ClinVar dbSNP
17	g.7673691_7673702del	CA645587404	TP53	c.919+2_919+13del c.523+2_523+13del c.640+2_640+13del c.898+2_898+13del c.782+482_782+493del (n.782+482_782+493del) c.802+2_802+13del c.442+2_442+13del c.886+2_886+13del	COSMIC COSMIC COSMIC COSMIC
17	g.7673689C>G	CA2733131997	TP53	c.919+12G>C (n.919+12G>C) c.523+12G>C (n.523+12G>C) c.640+12G>C (n.640+12G>C) c.898+12G>C (n.898+12G>C) c.782+492G>C (n.782+492G>C) c.802+12G>C (n.802+12G>C) c.442+12G>C (n.442+12G>C) c.886+12G>C (n.886+12G>C)	dbSNP
17	g.7673689C>T	CA2733132014	TP53	c.919+12G>A (n.919+12G>A) c.523+12G>A (n.523+12G>A) c.640+12G>A (n.640+12G>A) c.898+12G>A (n.898+12G>A) c.782+492G>A (n.782+492G>A) c.802+12G>A (n.802+12G>A) c.442+12G>A (n.442+12G>A) c.886+12G>A (n.886+12G>A)	dbSNP
17	g.7673690T>A	CA2733132023	TP53	c.919+11A>T (n.919+11A>T) c.523+11A>T (n.523+11A>T) c.640+11A>T (n.640+11A>T) c.898+11A>T (n.898+11A>T) c.782+491A>T (n.782+491A>T) c.802+11A>T (n.802+11A>T) c.442+11A>T (n.442+11A>T) c.886+11A>T (n.886+11A>T)	dbSNP
17	g.7673690T>C	CA2733132021	TP53	c.919+11A>G (n.919+11A>G) c.523+11A>G (n.523+11A>G) c.640+11A>G (n.640+11A>G) c.898+11A>G (n.898+11A>G) c.782+491A>G (n.782+491A>G) c.802+11A>G (n.802+11A>G) c.442+11A>G (n.442+11A>G) c.886+11A>G (n.886+11A>G)	dbSNP
17	g.7673690_7673703delinsTGCTTGCTTACCTC	CA2245948289	TP53	c.917_919+11delinsGAGGTAAGCAAGCA c.521_523+11delinsGAGGTAAGCAAGCA c.638_640+11delinsGAGGTAAGCAAGCA c.896_898+11delinsGAGGTAAGCAAGCA c.782+478_782+491delinsGAGGTAAGCAAGCA (n.782+478_782+491delinsGAGGTAAGCAAGCA) c.800_802+11delinsGAGGTAAGCAAGCA c.440_442+11delinsGAGGTAAGCAAGCA c.884_886+11delinsGAGGTAAGCAAGCA
17	g.7673691G>A	CA497714508	TP53	c.919+10C>T (n.919+10C>T) c.523+10C>T (n.523+10C>T) c.640+10C>T (n.640+10C>T) c.898+10C>T (n.898+10C>T) c.782+490C>T (n.782+490C>T) c.802+10C>T (n.802+10C>T) c.442+10C>T (n.442+10C>T) c.886+10C>T (n.886+10C>T)	dbSNP COSMIC
17	g.7673691G>C	CA2580094910	TP53	c.919+10C>G (n.919+10C>G) c.523+10C>G (n.523+10C>G) c.640+10C>G (n.640+10C>G) c.898+10C>G (n.898+10C>G) c.782+490C>G (n.782+490C>G) c.802+10C>G (n.802+10C>G) c.442+10C>G (n.442+10C>G) c.886+10C>G (n.886+10C>G)	ClinVar dbSNP
17	g.7673691G>T	CA2733132028	TP53	c.919+10C>A (n.919+10C>A) c.523+10C>A (n.523+10C>A) c.640+10C>A (n.640+10C>A) c.898+10C>A (n.898+10C>A) c.782+490C>A (n.782+490C>A) c.802+10C>A (n.802+10C>A) c.442+10C>A (n.442+10C>A) c.886+10C>A (n.886+10C>A)	dbSNP
17	g.7673691_7673696dup	CA2499306846	TP53	c.919+5_919+10dup (n.919+5_919+10dup) c.523+5_523+10dup (n.523+5_523+10dup) c.640+5_640+10dup (n.640+5_640+10dup) c.898+5_898+10dup (n.898+5_898+10dup) c.782+485_782+490dup (n.782+485_782+490dup) c.802+5_802+10dup (n.802+5_802+10dup) c.442+5_442+10dup (n.442+5_442+10dup) c.886+5_886+10dup (n.886+5_886+10dup)
17	g.7673695_7673707del	CA658798699	TP53	c.917_919+10del c.521_523+10del c.638_640+10del c.896_898+10del c.782+478_782+490del (n.782+478_782+490del) c.800_802+10del c.440_442+10del c.884_886+10del	ClinVar dbSNP
17	g.7673692C=	CA2245948296	TP53	c.919+9G= (n.919+9G=) c.523+9G= (n.523+9G=) c.640+9G= (n.640+9G=) c.898+9G= (n.898+9G=) c.782+489G= (n.782+489G=) c.802+9G= (n.802+9G=) c.442+9G= (n.442+9G=) c.886+9G= (n.886+9G=)
17	g.7673692C>G	CA2697559396	TP53	c.919+9G>C (n.919+9G>C) c.523+9G>C (n.523+9G>C) c.640+9G>C (n.640+9G>C) c.898+9G>C (n.898+9G>C) c.782+489G>C (n.782+489G>C) c.802+9G>C (n.802+9G>C) c.442+9G>C (n.442+9G>C) c.886+9G>C (n.886+9G>C)	ClinVar dbSNP
17	g.7673692C>T	CA001329	TP53	c.919+9G>A (n.919+9G>A) c.523+9G>A (n.523+9G>A) c.640+9G>A (n.640+9G>A) c.898+9G>A (n.898+9G>A) c.782+489G>A (n.782+489G>A) c.802+9G>A (n.802+9G>A) c.442+9G>A (n.442+9G>A) c.886+9G>A (n.886+9G>A)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673693T>A	CA2732963326	TP53	c.919+8A>T (n.919+8A>T) c.523+8A>T (n.523+8A>T) c.640+8A>T (n.640+8A>T) c.898+8A>T (n.898+8A>T) c.782+488A>T (n.782+488A>T) c.802+8A>T (n.802+8A>T) c.442+8A>T (n.442+8A>T) c.886+8A>T (n.886+8A>T)	dbSNP
17	g.7673693T>C	CA2732963325	TP53	c.919+8A>G (n.919+8A>G) c.523+8A>G (n.523+8A>G) c.640+8A>G (n.640+8A>G) c.898+8A>G (n.898+8A>G) c.782+488A>G (n.782+488A>G) c.802+8A>G (n.802+8A>G) c.442+8A>G (n.442+8A>G) c.886+8A>G (n.886+8A>G)	dbSNP
17	g.7673693T>G	CA658798700	TP53	c.919+8A>C (n.919+8A>C) c.523+8A>C (n.523+8A>C) c.640+8A>C (n.640+8A>C) c.898+8A>C (n.898+8A>C) c.782+488A>C (n.782+488A>C) c.802+8A>C (n.802+8A>C) c.442+8A>C (n.442+8A>C) c.886+8A>C (n.886+8A>C)	ClinVar dbSNP
17	g.7673693T=	CA2245948306	TP53	c.919+8A= (n.919+8A=) c.523+8A= (n.523+8A=) c.640+8A= (n.640+8A=) c.898+8A= (n.898+8A=) c.782+488A= (n.782+488A=) c.802+8A= (n.802+8A=) c.442+8A= (n.442+8A=) c.886+8A= (n.886+8A=)
17	g.7673694T>C	CA2732925636	TP53	c.919+7A>G (n.919+7A>G) c.523+7A>G (n.523+7A>G) c.640+7A>G (n.640+7A>G) c.898+7A>G (n.898+7A>G) c.782+487A>G (n.782+487A>G) c.802+7A>G (n.802+7A>G) c.442+7A>G (n.442+7A>G) c.886+7A>G (n.886+7A>G)	dbSNP
17	g.7673694T>G	CA001336	TP53	c.919+7A>C (n.919+7A>C) c.523+7A>C (n.523+7A>C) c.640+7A>C (n.640+7A>C) c.898+7A>C (n.898+7A>C) c.782+487A>C (n.782+487A>C) c.802+7A>C (n.802+7A>C) c.442+7A>C (n.442+7A>C) c.886+7A>C (n.886+7A>C)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673694T=	CA2245948313	TP53	c.919+7A= (n.919+7A=) c.523+7A= (n.523+7A=) c.640+7A= (n.640+7A=) c.898+7A= (n.898+7A=) c.782+487A= (n.782+487A=) c.802+7A= (n.802+7A=) c.442+7A= (n.442+7A=) c.886+7A= (n.886+7A=)
17	g.7673694_7673703delinsTGCTTACCTC	CA2245948319	TP53	c.917_919+7delinsGAGGTAAGCA c.521_523+7delinsGAGGTAAGCA c.638_640+7delinsGAGGTAAGCA c.896_898+7delinsGAGGTAAGCA c.782+478_782+487delinsGAGGTAAGCA (n.782+478_782+487delinsGAGGTAAGCA) c.800_802+7delinsGAGGTAAGCA c.440_442+7delinsGAGGTAAGCA c.884_886+7delinsGAGGTAAGCA
17	g.7673695G>A	CA497715301	TP53	c.919+6C>T (n.919+6C>T) c.523+6C>T (n.523+6C>T) c.640+6C>T (n.640+6C>T) c.898+6C>T (n.898+6C>T) c.782+486C>T (n.782+486C>T) c.802+6C>T (n.802+6C>T) c.442+6C>T (n.442+6C>T) c.886+6C>T (n.886+6C>T)	dbSNP COSMIC
17	g.7673695G>C	CA2635874555	TP53	c.919+6C>G (n.919+6C>G) c.523+6C>G (n.523+6C>G) c.640+6C>G (n.640+6C>G) c.898+6C>G (n.898+6C>G) c.782+486C>G (n.782+486C>G) c.802+6C>G (n.802+6C>G) c.442+6C>G (n.442+6C>G) c.886+6C>G (n.886+6C>G)	dbSNP gnomAD v4
17	g.7673695G>T	CA2733132314	TP53	c.919+6C>A (n.919+6C>A) c.523+6C>A (n.523+6C>A) c.640+6C>A (n.640+6C>A) c.898+6C>A (n.898+6C>A) c.782+486C>A (n.782+486C>A) c.802+6C>A (n.802+6C>A) c.442+6C>A (n.442+6C>A) c.886+6C>A (n.886+6C>A)	dbSNP
17	g.7673695dup	CA2635874554	TP53	c.919+6dup (n.919+6dup) c.523+6dup (n.523+6dup) c.640+6dup (n.640+6dup) c.898+6dup (n.898+6dup) c.782+486dup (n.782+486dup) c.802+6dup (n.802+6dup) c.442+6dup (n.442+6dup) c.886+6dup (n.886+6dup)	gnomAD v4
17	g.7673700_7673708del	CA891844040	TP53	c.917_919+6del c.521_523+6del c.638_640+6del c.896_898+6del c.782+478_782+486del (n.782+478_782+486del) c.800_802+6del c.440_442+6del c.884_886+6del	ClinVar dbSNP
17	g.7673696C>A	CA913190578	TP53	c.919+5G>T (n.919+5G>T) c.523+5G>T (n.523+5G>T) c.640+5G>T (n.640+5G>T) c.898+5G>T (n.898+5G>T) c.782+485G>T (n.782+485G>T) c.802+5G>T (n.802+5G>T) c.442+5G>T (n.442+5G>T) c.886+5G>T (n.886+5G>T)	ClinVar dbSNP
17	g.7673696C=	CA2245948333	TP53	c.919+5G= (n.919+5G=) c.523+5G= (n.523+5G=) c.640+5G= (n.640+5G=) c.898+5G= (n.898+5G=) c.782+485G= (n.782+485G=) c.802+5G= (n.802+5G=) c.442+5G= (n.442+5G=) c.886+5G= (n.886+5G=)
17	g.7673696C>G	CA338258	TP53	c.919+5G>C (n.919+5G>C) c.523+5G>C (n.523+5G>C) c.640+5G>C (n.640+5G>C) c.898+5G>C (n.898+5G>C) c.782+485G>C (n.782+485G>C) c.802+5G>C (n.802+5G>C) c.442+5G>C (n.442+5G>C) c.886+5G>C (n.886+5G>C)	ClinVar dbSNP gnomAD v4
17	g.7673696C>T	CA001342	TP53	c.919+5G>A (n.919+5G>A) c.523+5G>A (n.523+5G>A) c.640+5G>A (n.640+5G>A) c.898+5G>A (n.898+5G>A) c.782+485G>A (n.782+485G>A) c.802+5G>A (n.802+5G>A) c.442+5G>A (n.442+5G>A) c.886+5G>A (n.886+5G>A)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673696_7673703delinsTCCT	CA2831039394	TP53	c.917_919+5delinsAGGA c.521_523+5delinsAGGA c.638_640+5delinsAGGA c.896_898+5delinsAGGA c.782+478_782+485delinsAGGA (n.782+478_782+485delinsAGGA) c.800_802+5delinsAGGA c.440_442+5delinsAGGA c.884_886+5delinsAGGA
17	g.7673697T>A	CA2635874567	TP53	c.919+4A>T (n.919+4A>T) c.523+4A>T (n.523+4A>T) c.640+4A>T (n.640+4A>T) c.898+4A>T (n.898+4A>T) c.782+484A>T (n.782+484A>T) c.802+4A>T (n.802+4A>T) c.442+4A>T (n.442+4A>T) c.886+4A>T (n.886+4A>T)	dbSNP gnomAD v4
17	g.7673697T>C	CA2733132356	TP53	c.919+4A>G (n.919+4A>G) c.523+4A>G (n.523+4A>G) c.640+4A>G (n.640+4A>G) c.898+4A>G (n.898+4A>G) c.782+484A>G (n.782+484A>G) c.802+4A>G (n.802+4A>G) c.442+4A>G (n.442+4A>G) c.886+4A>G (n.886+4A>G)	dbSNP
17	g.7673698dup	CA2635874565	TP53	c.919+4dup (n.919+4dup) c.523+4dup (n.523+4dup) c.640+4dup (n.640+4dup) c.898+4dup (n.898+4dup) c.782+484dup (n.782+484dup) c.802+4dup (n.802+4dup) c.442+4dup (n.442+4dup) c.886+4dup (n.886+4dup)	gnomAD v4
17	g.7673698T>A	CA2635874568	TP53	c.919+3A>T (n.919+3A>T) c.523+3A>T (n.523+3A>T) c.640+3A>T (n.640+3A>T) c.898+3A>T (n.898+3A>T) c.782+483A>T (n.782+483A>T) c.802+3A>T (n.802+3A>T) c.442+3A>T (n.442+3A>T) c.886+3A>T (n.886+3A>T)	gnomAD v4
17	g.7673698T>C	CA10580911	TP53	c.919+3A>G (n.919+3A>G) c.523+3A>G (n.523+3A>G) c.640+3A>G (n.640+3A>G) c.898+3A>G (n.898+3A>G) c.782+483A>G (n.782+483A>G) c.802+3A>G (n.802+3A>G) c.442+3A>G (n.442+3A>G) c.886+3A>G (n.886+3A>G)	ClinVar dbSNP gnomAD v4
17	g.7673698T=	CA2245948340	TP53	c.919+3A= (n.919+3A=) c.523+3A= (n.523+3A=) c.640+3A= (n.640+3A=) c.898+3A= (n.898+3A=) c.782+483A= (n.782+483A=) c.802+3A= (n.802+3A=) c.442+3A= (n.442+3A=) c.886+3A= (n.886+3A=)
17	g.7673699del	CA497715315	TP53	c.919+2del (n.919+2del) c.523+2del (n.523+2del) c.640+2del (n.640+2del) c.898+2del (n.898+2del) c.782+482del (n.782+482del) c.802+2del (n.802+2del) c.442+2del (n.442+2del) c.886+2del (n.886+2del)	COSMIC
17	g.7673699A=	CA2245948351	TP53	c.919+2T= (n.919+2T=) c.523+2T= (n.523+2T=) c.640+2T= (n.640+2T=) c.898+2T= (n.898+2T=) c.782+482T= (n.782+482T=) c.802+2T= (n.802+2T=) c.442+2T= (n.442+2T=) c.886+2T= (n.886+2T=)
17	g.7673699A>C	CA397836235	TP53	c.919+2T>G (n.919+2T>G) c.523+2T>G (n.523+2T>G) c.640+2T>G (n.640+2T>G) c.898+2T>G (n.898+2T>G) c.782+482T>G (n.782+482T>G) c.802+2T>G (n.802+2T>G) c.442+2T>G (n.442+2T>G) c.886+2T>G (n.886+2T>G)	ClinVar dbSNP
17	g.7673699A>G	CA397836238	TP53	c.919+2T>C (n.919+2T>C) c.523+2T>C (n.523+2T>C) c.640+2T>C (n.640+2T>C) c.898+2T>C (n.898+2T>C) c.782+482T>C (n.782+482T>C) c.802+2T>C (n.802+2T>C) c.442+2T>C (n.442+2T>C) c.886+2T>C (n.886+2T>C)	dbSNP
17	g.7673699A>T	CA397836240	TP53	c.919+2T>A (n.919+2T>A) c.523+2T>A (n.523+2T>A) c.640+2T>A (n.640+2T>A) c.898+2T>A (n.898+2T>A) c.782+482T>A (n.782+482T>A) c.802+2T>A (n.802+2T>A) c.442+2T>A (n.442+2T>A) c.886+2T>A (n.886+2T>A)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673700C>A	CA397836242	TP53	c.919+1G>T (n.919+1G>T) c.523+1G>T (n.523+1G>T) c.640+1G>T (n.640+1G>T) c.898+1G>T (n.898+1G>T) c.782+481G>T (n.782+481G>T) c.802+1G>T (n.802+1G>T) c.442+1G>T (n.442+1G>T) c.886+1G>T (n.886+1G>T)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673700C=	CA2245948372	TP53	c.919+1G= (n.919+1G=) c.523+1G= (n.523+1G=) c.640+1G= (n.640+1G=) c.898+1G= (n.898+1G=) c.782+481G= (n.782+481G=) c.802+1G= (n.802+1G=) c.442+1G= (n.442+1G=) c.886+1G= (n.886+1G=)
17	g.7673700C>G	CA397836244	TP53	c.919+1G>C (n.919+1G>C) c.523+1G>C (n.523+1G>C) c.640+1G>C (n.640+1G>C) c.898+1G>C (n.898+1G>C) c.782+481G>C (n.782+481G>C) c.802+1G>C (n.802+1G>C) c.442+1G>C (n.442+1G>C) c.886+1G>C (n.886+1G>C)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673700C>T	CA397836247	TP53	c.919+1G>A (n.919+1G>A) c.523+1G>A (n.523+1G>A) c.640+1G>A (n.640+1G>A) c.898+1G>A (n.898+1G>A) c.782+481G>A (n.782+481G>A) c.802+1G>A (n.802+1G>A) c.442+1G>A (n.442+1G>A) c.886+1G>A (n.886+1G>A)	ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17	g.7673701del	CA497715326	TP53	c.919+1del c.523+1del c.640+1del c.898+1del c.782+481del (n.782+481del) c.802+1del c.442+1del c.886+1del	ClinVar dbSNP COSMIC
17	g.7673701C>A	CA397836255	TP53	c.919G>T (p.Ala307Ser) c.523G>T (p.Ala175Ser) c.640G>T (p.Ala214Ser) c.898G>T (p.Ala300Ser) c.782+480G>T (n.782+480G>T) c.802G>T (p.Ala268Ser) c.442G>T (p.Ala148Ser) c.886G>T (p.Ala296Ser)	dbSNP COSMIC
17	g.7673701C>G	CA397836258	TP53	c.919G>C (p.Ala307Pro) c.523G>C (p.Ala175Pro) c.640G>C (p.Ala214Pro) c.898G>C (p.Ala300Pro) c.782+480G>C (n.782+480G>C) c.802G>C (p.Ala268Pro) c.442G>C (p.Ala148Pro) c.886G>C (p.Ala296Pro)	ClinVar dbSNP
17	g.7673701C>T	CA397836252	TP53	c.919G>A (p.Ala307Thr) c.523G>A (p.Ala175Thr) c.640G>A (p.Ala214Thr) c.898G>A (p.Ala300Thr) c.782+480G>A (n.782+480G>A) c.802G>A (p.Ala268Thr) c.442G>A (p.Ala148Thr) c.886G>A (p.Ala296Thr)	ClinVar dbSNP COSMIC
17	g.7673702_7673703del	CA645587409	TP53	c.918_919del (p.Ala307ThrfsTer29) c.522_523del (p.Ala175ThrfsTer29) c.639_640del (p.Ala214ThrfsTer29) c.897_898del (p.Ala300ThrfsTer29) c.918_919del (p.Ala307ThrfsTer?) c.782+479_782+480del (n.782+479_782+480del) c.918_919del (p.Ala307ThrfsTer28) c.522_523del (p.Ala175ThrfsTer28) c.522_523del (p.Ala175ThrfsTer?) c.801_802del (p.Ala268ThrfsTer29) c.801_802del (p.Ala268ThrfsTer28) c.441_442del (p.Ala148ThrfsTer28) c.885_886del (p.Ala296ThrfsTer29) c.441_442del (p.Ala148ThrfsTer?) c.441_442del (p.Ala148ThrfsTer29) c.801_802del (p.Ala268ThrfsTer?)	COSMIC COSMIC
17	g.7673705_7673729dup	CA916081896	TP53	c.895_919dup (p.Leu308AlafsTer6) c.499_523dup (p.Leu176AlafsTer6) c.616_640dup (p.Leu215AlafsTer6) c.874_898dup (p.Leu301AlafsTer6) c.782+456_782+480dup (n.782+456_782+480dup) c.778_802dup (p.Leu269AlafsTer6) c.418_442dup (p.Leu149AlafsTer6) c.862_886dup (p.Leu297AlafsTer6)	ClinVar dbSNP
17	g.7673701_7673702insCG	CA645587413	TP53	c.918_919insCG (p.Ala307ArgfsTer?) c.522_523insCG (p.Ala175ArgfsTer?) c.639_640insCG (p.Ala214ArgfsTer?) c.897_898insCG (p.Ala300ArgfsTer?) c.782+479_782+480insCG (n.782+479_782+480insCG) c.801_802insCG (p.Ala268ArgfsTer?) c.441_442insCG (p.Ala148ArgfsTer?) c.885_886insCG (p.Ala296ArgfsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673702T>A	CA497715338	TP53	c.918A>T (p.Arg306=) c.522A>T (p.Arg174=) c.639A>T (p.Arg213=) c.897A>T (p.Arg299=) c.782+479A>T (n.782+479A>T) c.801A>T (p.Arg267=) c.441A>T (p.Arg147=) c.885A>T (p.Arg295=)	ClinVar dbSNP COSMIC
17	g.7673702T>C	CA497715340	TP53	c.918A>G (p.Arg306=) c.522A>G (p.Arg174=) c.639A>G (p.Arg213=) c.897A>G (p.Arg299=) c.782+479A>G (n.782+479A>G) c.801A>G (p.Arg267=) c.441A>G (p.Arg147=) c.885A>G (p.Arg295=)	dbSNP gnomAD v4
17	g.7673702T>G	CA497715341	TP53	c.918A>C (p.Arg306=) c.522A>C (p.Arg174=) c.639A>C (p.Arg213=) c.897A>C (p.Arg299=) c.782+479A>C (n.782+479A>C) c.801A>C (p.Arg267=) c.441A>C (p.Arg147=) c.885A>C (p.Arg295=)
17	g.7673702_7673703insAAGGAGT	CA645587410	TP53	c.918_919insCTCCTTA (p.Ala307LeufsTer32) c.522_523insCTCCTTA (p.Ala175LeufsTer32) c.639_640insCTCCTTA (p.Ala214LeufsTer32) c.897_898insCTCCTTA (p.Ala300LeufsTer32) c.918_919insCTCCTTA (p.Ala307LeufsTer?) c.782+479_782+480insCTCCTTA (n.782+479_782+480insCTCCTTA) c.918_919insCTCCTTA (p.Ala307LeufsTer31) c.522_523insCTCCTTA (p.Ala175LeufsTer31) c.522_523insCTCCTTA (p.Ala175LeufsTer?) c.801_802insCTCCTTA (p.Ala268LeufsTer32) c.801_802insCTCCTTA (p.Ala268LeufsTer31) c.441_442insCTCCTTA (p.Ala148LeufsTer31) c.885_886insCTCCTTA (p.Ala296LeufsTer32) c.441_442insCTCCTTA (p.Ala148LeufsTer?) c.441_442insCTCCTTA (p.Ala148LeufsTer32) c.801_802insCTCCTTA (p.Ala268LeufsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673702dup	CA645587411	TP53	c.918dup (p.Ala307SerfsTer30) c.522dup (p.Ala175SerfsTer30) c.639dup (p.Ala214SerfsTer30) c.897dup (p.Ala300SerfsTer30) c.918dup (p.Ala307SerfsTer?) c.782+479dup (n.782+479dup) c.918dup (p.Ala307SerfsTer29) c.522dup (p.Ala175SerfsTer29) c.522dup (p.Ala175SerfsTer?) c.801dup (p.Ala268SerfsTer30) c.801dup (p.Ala268SerfsTer29) c.441dup (p.Ala148SerfsTer29) c.885dup (p.Ala296SerfsTer30) c.441dup (p.Ala148SerfsTer?) c.441dup (p.Ala148SerfsTer30) c.801dup (p.Ala268SerfsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673703C>A	CA397836260	TP53	c.917G>T (p.Arg306Leu) c.521G>T (p.Arg174Leu) c.638G>T (p.Arg213Leu) c.896G>T (p.Arg299Leu) c.782+478G>T (n.782+478G>T) c.800G>T (p.Arg267Leu) c.440G>T (p.Arg147Leu) c.884G>T (p.Arg295Leu)	dbSNP
17	g.7673703C=	CA2245948393	TP53	c.917G= (p.Arg306=) c.521G= (p.Arg174=) c.638G= (p.Arg213=) c.896G= (p.Arg299=) c.782+478G= (n.782+478G=) c.800G= (p.Arg267=) c.440G= (p.Arg147=) c.884G= (p.Arg295=)
17	g.7673703C>G	CA397836262	TP53	c.917G>C (p.Arg306Pro) c.521G>C (p.Arg174Pro) c.638G>C (p.Arg213Pro) c.896G>C (p.Arg299Pro) c.782+478G>C (n.782+478G>C) c.800G>C (p.Arg267Pro) c.440G>C (p.Arg147Pro) c.884G>C (p.Arg295Pro)	dbSNP
17	g.7673703C>T	CA287486566	TP53	c.917G>A (p.Arg306Gln) c.521G>A (p.Arg174Gln) c.638G>A (p.Arg213Gln) c.896G>A (p.Arg299Gln) c.782+478G>A (n.782+478G>A) c.800G>A (p.Arg267Gln) c.440G>A (p.Arg147Gln) c.884G>A (p.Arg295Gln)	ClinVar dbSNP gnomAD v2 gnomAD v4
17	g.7673704_7673716dup	CA2739265584	TP53	c.905_917dup (p.Ala307GlufsTer3) c.509_521dup (p.Ala175GlufsTer3) c.626_638dup (p.Ala214GlufsTer3) c.884_896dup (p.Ala300GlufsTer3) c.782+466_782+478dup (n.782+466_782+478dup) c.788_800dup (p.Ala268GlufsTer3) c.428_440dup (p.Ala148GlufsTer3) c.872_884dup (p.Ala296GlufsTer3)	ClinVar
17	g.7673703_7673704insCTTA	CA645587415	TP53	c.916_917insTAAG (p.Arg306LeufsTer?) c.520_521insTAAG (p.Arg174LeufsTer?) c.637_638insTAAG (p.Arg213LeufsTer?) c.895_896insTAAG (p.Arg299LeufsTer?) c.782+477_782+478insTAAG (n.782+477_782+478insTAAG) c.916_917insTAAG (p.Arg306LeufsTer31) c.520_521insTAAG (p.Arg174LeufsTer31) c.799_800insTAAG (p.Arg267LeufsTer?) c.799_800insTAAG (p.Arg267LeufsTer31) c.439_440insTAAG (p.Arg147LeufsTer31) c.883_884insTAAG (p.Arg295LeufsTer?) c.439_440insTAAG (p.Arg147LeufsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673704del	CA497715354	TP53	c.916del (p.Arg306GlufsTer?) c.520del (p.Arg174GlufsTer?) c.637del (p.Arg213GlufsTer?) c.895del (p.Arg299GlufsTer?) c.782+477del (n.782+477del) c.799del (p.Arg267GlufsTer?) c.439del (p.Arg147GlufsTer?) c.883del (p.Arg295GlufsTer?)	COSMIC
17	g.7673704G>A	CA000495	TP53	c.916C>T (p.Arg306Ter) c.520C>T (p.Arg174Ter) c.637C>T (p.Arg213Ter) c.895C>T (p.Arg299Ter) c.782+477C>T (n.782+477C>T) c.799C>T (p.Arg267Ter) c.439C>T (p.Arg147Ter) c.883C>T (p.Arg295Ter)	ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17	g.7673704G>C	CA397836267	TP53	c.916C>G (p.Arg306Gly) c.520C>G (p.Arg174Gly) c.637C>G (p.Arg213Gly) c.895C>G (p.Arg299Gly) c.782+477C>G (n.782+477C>G) c.799C>G (p.Arg267Gly) c.439C>G (p.Arg147Gly) c.883C>G (p.Arg295Gly)	dbSNP
17	g.7673704G=	CA2245948417	TP53	c.916C= (p.Arg306=) c.520C= (p.Arg174=) c.637C= (p.Arg213=) c.895C= (p.Arg299=) c.782+477C= (n.782+477C=) c.799C= (p.Arg267=) c.439C= (p.Arg147=) c.883C= (p.Arg295=)
17	g.7673704G>T	CA497715351	TP53	c.916C>A (p.Arg306=) c.520C>A (p.Arg174=) c.637C>A (p.Arg213=) c.895C>A (p.Arg299=) c.782+477C>A (n.782+477C>A) c.799C>A (p.Arg267=) c.439C>A (p.Arg147=) c.883C>A (p.Arg295=)	ClinVar dbSNP
17	g.7673704_7673707del	CA2695224217	TP53	c.913_916del (p.Lys305GlufsTer?) c.517_520del (p.Lys173GlufsTer?) c.634_637del (p.Lys212GlufsTer?) c.892_895del (p.Lys298GlufsTer?) c.782+474_782+477del (n.782+474_782+477del) c.796_799del (p.Lys266GlufsTer?) c.436_439del (p.Lys146GlufsTer?) c.880_883del (p.Lys294GlufsTer?)
17	g.7673704_7673707dup	CA2695224218	TP53	c.913_916dup (p.Arg306GlnfsTer?) c.517_520dup (p.Arg174GlnfsTer?) c.634_637dup (p.Arg213GlnfsTer?) c.892_895dup (p.Arg299GlnfsTer?) c.782+474_782+477dup (n.782+474_782+477dup) c.913_916dup (p.Arg306GlnfsTer31) c.517_520dup (p.Arg174GlnfsTer31) c.796_799dup (p.Arg267GlnfsTer?) c.796_799dup (p.Arg267GlnfsTer31) c.436_439dup (p.Arg147GlnfsTer31) c.880_883dup (p.Arg295GlnfsTer?) c.436_439dup (p.Arg147GlnfsTer?)
17	g.7673704_7673711dup	CA915949520	TP53	c.909_916dup (p.Arg306ProfsTer?) c.513_520dup (p.Arg174ProfsTer?) c.630_637dup (p.Arg213ProfsTer?) c.888_895dup (p.Arg299ProfsTer?) c.782+470_782+477dup (n.782+470_782+477dup) c.792_799dup (p.Arg267ProfsTer?) c.432_439dup (p.Arg147ProfsTer?) c.876_883dup (p.Arg295ProfsTer?)	ClinVar dbSNP
17	g.7673705_7673721dup	CA2825002634	TP53	c.900_916dup (p.Arg306ProfsTer?) c.504_520dup (p.Arg174ProfsTer?) c.621_637dup (p.Arg213ProfsTer?) c.879_895dup (p.Arg299ProfsTer?) c.782+461_782+477dup (n.782+461_782+477dup) c.783_799dup (p.Arg267ProfsTer?) c.423_439dup (p.Arg147ProfsTer?) c.867_883dup (p.Arg295ProfsTer?)	ClinVar
17	g.7673705_7673827del	CA645587414	TP53	c.794_916del (p.Leu265_Lys305del) c.398_520del (p.Leu133_Lys173del) c.515_637del (p.Leu172_Lys212del) c.773_895del (p.Leu258_Lys298del) c.782+355_782+477del (n.782+355_782+477del) c.677_799del (p.Leu226_Lys266del) c.317_439del (p.Leu106_Lys146del) c.761_883del (p.Leu254_Lys294del)	COSMIC
17	g.7673705C>A	CA397836273	TP53	c.915G>T (p.Lys305Asn) c.519G>T (p.Lys173Asn) c.636G>T (p.Lys212Asn) c.894G>T (p.Lys298Asn) c.782+476G>T (n.782+476G>T) c.798G>T (p.Lys266Asn) c.438G>T (p.Lys146Asn) c.882G>T (p.Lys294Asn)	COSMIC
17	g.7673705C>G	CA397836270	TP53	c.915G>C (p.Lys305Asn) c.519G>C (p.Lys173Asn) c.636G>C (p.Lys212Asn) c.894G>C (p.Lys298Asn) c.782+476G>C (n.782+476G>C) c.798G>C (p.Lys266Asn) c.438G>C (p.Lys146Asn) c.882G>C (p.Lys294Asn)	COSMIC
17	g.7673705C>T	CA497715358	TP53	c.915G>A (p.Lys305=) c.519G>A (p.Lys173=) c.636G>A (p.Lys212=) c.894G>A (p.Lys298=) c.782+476G>A (n.782+476G>A) c.798G>A (p.Lys266=) c.438G>A (p.Lys146=) c.882G>A (p.Lys294=)	ClinVar dbSNP COSMIC
17	g.7673705_7673707delinsTTA	CA645587416	TP53	c.913_915delinsTAA (p.Lys305Ter) c.517_519delinsTAA (p.Lys173Ter) c.634_636delinsTAA (p.Lys212Ter) c.892_894delinsTAA (p.Lys298Ter) c.782+474_782+476delinsTAA (n.782+474_782+476delinsTAA) c.796_798delinsTAA (p.Lys266Ter) c.436_438delinsTAA (p.Lys146Ter) c.880_882delinsTAA (p.Lys294Ter)	COSMIC
17	g.7673706T>A	CA397836276	TP53	c.914A>T (p.Lys305Met) c.518A>T (p.Lys173Met) c.635A>T (p.Lys212Met) c.893A>T (p.Lys298Met) c.782+475A>T (n.782+475A>T) c.797A>T (p.Lys266Met) c.437A>T (p.Lys146Met) c.881A>T (p.Lys294Met)	dbSNP
17	g.7673706T>C	CA397836278	TP53	c.914A>G (p.Lys305Arg) c.518A>G (p.Lys173Arg) c.635A>G (p.Lys212Arg) c.893A>G (p.Lys298Arg) c.782+475A>G (n.782+475A>G) c.797A>G (p.Lys266Arg) c.437A>G (p.Lys146Arg) c.881A>G (p.Lys294Arg)	dbSNP gnomAD v4 COSMIC
17	g.7673706T>G	CA397836279	TP53	c.914A>C (p.Lys305Thr) c.518A>C (p.Lys173Thr) c.635A>C (p.Lys212Thr) c.893A>C (p.Lys298Thr) c.782+475A>C (n.782+475A>C) c.797A>C (p.Lys266Thr) c.437A>C (p.Lys146Thr) c.881A>C (p.Lys294Thr)	COSMIC
17	g.7673707del	CA891842225	TP53	c.914del (p.Lys305SerfsTer?) c.518del (p.Lys173SerfsTer?) c.635del (p.Lys212SerfsTer?) c.893del (p.Lys298SerfsTer?) c.782+475del (n.782+475del) c.797del (p.Lys266SerfsTer?) c.437del (p.Lys146SerfsTer?) c.881del (p.Lys294SerfsTer?)
17	g.7673707T>A	CA397836281	TP53	c.913A>T (p.Lys305Ter) c.517A>T (p.Lys173Ter) c.634A>T (p.Lys212Ter) c.892A>T (p.Lys298Ter) c.782+474A>T (n.782+474A>T) c.796A>T (p.Lys266Ter) c.436A>T (p.Lys146Ter) c.880A>T (p.Lys294Ter)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673707T>C	CA397836283	TP53	c.913A>G (p.Lys305Glu) c.517A>G (p.Lys173Glu) c.634A>G (p.Lys212Glu) c.892A>G (p.Lys298Glu) c.782+474A>G (n.782+474A>G) c.796A>G (p.Lys266Glu) c.436A>G (p.Lys146Glu) c.880A>G (p.Lys294Glu)	dbSNP COSMIC
17	g.7673707T>G	CA397836286	TP53	c.913A>C (p.Lys305Gln) c.517A>C (p.Lys173Gln) c.634A>C (p.Lys212Gln) c.892A>C (p.Lys298Gln) c.782+474A>C (n.782+474A>C) c.796A>C (p.Lys266Gln) c.436A>C (p.Lys146Gln) c.880A>C (p.Lys294Gln)	dbSNP
17	g.7673707T=	CA2245948423	TP53	c.913A= (p.Lys305=) c.517A= (p.Lys173=) c.634A= (p.Lys212=) c.892A= (p.Lys298=) c.782+474A= (n.782+474A=) c.796A= (p.Lys266=) c.436A= (p.Lys146=) c.880A= (p.Lys294=)
17	g.7673708A=	CA2245948439	TP53	c.912T= (p.Thr304=) c.516T= (p.Thr172=) c.633T= (p.Thr211=) c.891T= (p.Thr297=) c.782+473T= (n.782+473T=) c.795T= (p.Thr265=) c.435T= (p.Thr145=) c.879T= (p.Thr293=)
17	g.7673708A>C	CA497715374	TP53	c.912T>G (p.Thr304=) c.516T>G (p.Thr172=) c.633T>G (p.Thr211=) c.891T>G (p.Thr297=) c.782+473T>G (n.782+473T>G) c.795T>G (p.Thr265=) c.435T>G (p.Thr145=) c.879T>G (p.Thr293=)	COSMIC
17	g.7673708A>G	CA497715375	TP53	c.912T>C (p.Thr304=) c.516T>C (p.Thr172=) c.633T>C (p.Thr211=) c.891T>C (p.Thr297=) c.782+473T>C (n.782+473T>C) c.795T>C (p.Thr265=) c.435T>C (p.Thr145=) c.879T>C (p.Thr293=)	ClinVar dbSNP
17	g.7673708A>T	CA497715376	TP53	c.912T>A (p.Thr304=) c.516T>A (p.Thr172=) c.633T>A (p.Thr211=) c.891T>A (p.Thr297=) c.782+473T>A (n.782+473T>A) c.795T>A (p.Thr265=) c.435T>A (p.Thr145=) c.879T>A (p.Thr293=)	dbSNP
17	g.7673708dup	CA913188786	TP53	c.912dup (p.Lys305Ter) c.516dup (p.Lys173Ter) c.633dup (p.Lys212Ter) c.891dup (p.Lys298Ter) c.782+473dup (n.782+473dup) c.795dup (p.Lys266Ter) c.435dup (p.Lys146Ter) c.879dup (p.Lys294Ter)	ClinVar dbSNP
17	g.7673708_7673710delinsAGT	CA2245948435	TP53	c.910_912delinsACT (p.Thr304=) c.514_516delinsACT (p.Thr172=) c.631_633delinsACT (p.Thr211=) c.889_891delinsACT (p.Thr297=) c.782+471_782+473delinsACT (n.782+471_782+473delinsACT) c.793_795delinsACT (p.Thr265=) c.433_435delinsACT (p.Thr145=) c.877_879delinsACT (p.Thr293=)
17	g.7673708_7673742dup	CA2582342142	TP53	c.878_912dup (p.Lys305GlyfsTer?) c.482_516dup (p.Lys173GlyfsTer?) c.599_633dup (p.Lys212GlyfsTer?) c.857_891dup (p.Lys298GlyfsTer?) c.782+439_782+473dup (n.782+439_782+473dup) c.761_795dup (p.Lys266GlyfsTer?) c.401_435dup (p.Lys146GlyfsTer?) c.845_879dup (p.Lys294GlyfsTer?)	ClinVar
17	g.7673709del	CA645587418	TP53	c.911del (p.Thr304IlefsTer?) c.515del (p.Thr172IlefsTer?) c.632del (p.Thr211IlefsTer?) c.890del (p.Thr297IlefsTer?) c.782+472del (n.782+472del) c.794del (p.Thr265IlefsTer?) c.434del (p.Thr145IlefsTer?) c.878del (p.Thr293IlefsTer?)	dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673709G>A	CA397836290	TP53	c.911C>T (p.Thr304Ile) c.515C>T (p.Thr172Ile) c.632C>T (p.Thr211Ile) c.890C>T (p.Thr297Ile) c.782+472C>T (n.782+472C>T) c.794C>T (p.Thr265Ile) c.434C>T (p.Thr145Ile) c.878C>T (p.Thr293Ile)	ClinVar dbSNP COSMIC
17	g.7673709G>C	CA397836295	TP53	c.911C>G (p.Thr304Ser) c.515C>G (p.Thr172Ser) c.632C>G (p.Thr211Ser) c.890C>G (p.Thr297Ser) c.782+472C>G (n.782+472C>G) c.794C>G (p.Thr265Ser) c.434C>G (p.Thr145Ser) c.878C>G (p.Thr293Ser)	dbSNP
17	g.7673709G=	CA2245948452	TP53	c.911C= (p.Thr304=) c.515C= (p.Thr172=) c.632C= (p.Thr211=) c.890C= (p.Thr297=) c.782+472C= (n.782+472C=) c.794C= (p.Thr265=) c.434C= (p.Thr145=) c.878C= (p.Thr293=)
17	g.7673709G>T	CA397836292	TP53	c.911C>A (p.Thr304Asn) c.515C>A (p.Thr172Asn) c.632C>A (p.Thr211Asn) c.890C>A (p.Thr297Asn) c.782+472C>A (n.782+472C>A) c.794C>A (p.Thr265Asn) c.434C>A (p.Thr145Asn) c.878C>A (p.Thr293Asn)	COSMIC
17	g.7673709_7673710delinsCCTTGCTTACCTC	CA1139665114	TP53	c.910_911delinsGAGGTAAGCAAGG (p.Thr304GlufsTer?) c.514_515delinsGAGGTAAGCAAGG (p.Thr172GlufsTer?) c.631_632delinsGAGGTAAGCAAGG (p.Thr211GlufsTer?) c.889_890delinsGAGGTAAGCAAGG (p.Thr297GlufsTer?) c.782+471_782+472delinsGAGGTAAGCAAGG (n.782+471_782+472delinsGAGGTAAGCAAGG) c.793_794delinsGAGGTAAGCAAGG (p.Thr265GlufsTer?) c.433_434delinsGAGGTAAGCAAGG (p.Thr145GlufsTer?) c.877_878delinsGAGGTAAGCAAGG (p.Thr293GlufsTer?)	ClinVar dbSNP
17	g.7673709_7673743del	CA645587417	TP53	c.877_911del (p.Gly293Ter) c.481_515del (p.Gly161Ter) c.598_632del (p.Gly200Ter) c.856_890del (p.Gly286Ter) c.782+438_782+472del (n.782+438_782+472del) c.760_794del (p.Gly254Ter) c.400_434del (p.Gly134Ter) c.844_878del (p.Gly282Ter)	COSMIC
17	g.7673710del	CA497715392	TP53	c.910del (p.Thr304LeufsTer?) c.514del (p.Thr172LeufsTer?) c.631del (p.Thr211LeufsTer?) c.889del (p.Thr297LeufsTer?) c.782+471del (n.782+471del) c.793del (p.Thr265LeufsTer?) c.433del (p.Thr145LeufsTer?) c.877del (p.Thr293LeufsTer?)	COSMIC
17	g.7673710T>A	CA397836298	TP53	c.910A>T (p.Thr304Ser) c.514A>T (p.Thr172Ser) c.631A>T (p.Thr211Ser) c.889A>T (p.Thr297Ser) c.782+471A>T (n.782+471A>T) c.793A>T (p.Thr265Ser) c.433A>T (p.Thr145Ser) c.877A>T (p.Thr293Ser)
17	g.7673710T>C	CA000493	TP53	c.910A>G (p.Thr304Ala) c.514A>G (p.Thr172Ala) c.631A>G (p.Thr211Ala) c.889A>G (p.Thr297Ala) c.782+471A>G (n.782+471A>G) c.793A>G (p.Thr265Ala) c.433A>G (p.Thr145Ala) c.877A>G (p.Thr293Ala)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17	g.7673710T>G	CA397836301	TP53	c.910A>C (p.Thr304Pro) c.514A>C (p.Thr172Pro) c.631A>C (p.Thr211Pro) c.889A>C (p.Thr297Pro) c.782+471A>C (n.782+471A>C) c.793A>C (p.Thr265Pro) c.433A>C (p.Thr145Pro) c.877A>C (p.Thr293Pro)
17	g.7673710T=	CA2245948462	TP53	c.910A= (p.Thr304=) c.514A= (p.Thr172=) c.631A= (p.Thr211=) c.889A= (p.Thr297=) c.782+471A= (n.782+471A=) c.793A= (p.Thr265=) c.433A= (p.Thr145=) c.877A= (p.Thr293=)
17	g.7673710_7673713dup	CA1139771733	TP53	c.907_910dup (p.Thr304LysfsTer3) c.511_514dup (p.Thr172LysfsTer3) c.628_631dup (p.Thr211LysfsTer3) c.886_889dup (p.Thr297LysfsTer3) c.782+468_782+471dup (n.782+468_782+471dup) c.790_793dup (p.Thr265LysfsTer3) c.430_433dup (p.Thr145LysfsTer3) c.874_877dup (p.Thr293LysfsTer3)	ClinVar
17	g.7673710_7673724delinsTGCTCCCTGGGGGCA	CA2245948463	TP53	c.896_910delinsTGCCCCCAGGGAGCA (p.Leu299=) c.500_514delinsTGCCCCCAGGGAGCA (p.Leu167=) c.617_631delinsTGCCCCCAGGGAGCA (p.Leu206=) c.875_889delinsTGCCCCCAGGGAGCA (p.Leu292=) c.782+457_782+471delinsTGCCCCCAGGGAGCA (n.782+457_782+471delinsTGCCCCCAGGGAGCA) c.779_793delinsTGCCCCCAGGGAGCA (p.Leu260=) c.419_433delinsTGCCCCCAGGGAGCA (p.Leu140=) c.863_877delinsTGCCCCCAGGGAGCA (p.Leu288=)
17	g.7673711G>A	CA497715400	TP53	c.909C>T (p.Ser303=) c.513C>T (p.Ser171=) c.630C>T (p.Ser210=) c.888C>T (p.Ser296=) c.782+470C>T (n.782+470C>T) c.792C>T (p.Ser264=) c.432C>T (p.Ser144=) c.876C>T (p.Ser292=)	ClinVar dbSNP gnomAD v3 gnomAD v4
17	g.7673711G>C	CA397836305	TP53	c.909C>G (p.Ser303Arg) c.513C>G (p.Ser171Arg) c.630C>G (p.Ser210Arg) c.888C>G (p.Ser296Arg) c.782+470C>G (n.782+470C>G) c.792C>G (p.Ser264Arg) c.432C>G (p.Ser144Arg) c.876C>G (p.Ser292Arg)	ClinVar dbSNP gnomAD v4
17	g.7673711G=	CA2245948472	TP53	c.909C= (p.Ser303=) c.513C= (p.Ser171=) c.630C= (p.Ser210=) c.888C= (p.Ser296=) c.782+470C= (n.782+470C=) c.792C= (p.Ser264=) c.432C= (p.Ser144=) c.876C= (p.Ser292=)
17	g.7673711G>T	CA397836307	TP53	c.909C>A (p.Ser303Arg) c.513C>A (p.Ser171Arg) c.630C>A (p.Ser210Arg) c.888C>A (p.Ser296Arg) c.782+470C>A (n.782+470C>A) c.792C>A (p.Ser264Arg) c.432C>A (p.Ser144Arg) c.876C>A (p.Ser292Arg)	dbSNP
17	g.7673712_7673720del	CA645587420	TP53	c.901_909del (p.Pro301_Ser303del) c.505_513del (p.Pro169_Ser171del) c.622_630del (p.Pro208_Ser210del) c.880_888del (p.Pro294_Ser296del) c.782+462_782+470del (n.782+462_782+470del) c.784_792del (p.Pro262_Ser264del) c.424_432del (p.Pro142_Ser144del) c.868_876del (p.Pro290_Ser292del)	COSMIC
17	g.7673715_7673728del	CA645587421	TP53	c.896_909del (p.Leu299HisfsTer2) c.500_513del (p.Leu167HisfsTer2) c.617_630del (p.Leu206HisfsTer2) c.875_888del (p.Leu292HisfsTer2) c.782+457_782+470del (n.782+457_782+470del) c.779_792del (p.Leu260HisfsTer2) c.419_432del (p.Leu140HisfsTer2) c.863_876del (p.Leu288HisfsTer2)	ClinVar dbSNP COSMIC
17	g.7673711_7673734del	CA645587419	TP53	c.886_909del (p.His296_Ser303del) c.490_513del (p.His164_Ser171del) c.607_630del (p.His203_Ser210del) c.865_888del (p.His289_Ser296del) c.782+447_782+470del (n.782+447_782+470del) c.769_792del (p.His257_Ser264del) c.409_432del (p.His137_Ser144del) c.853_876del (p.His285_Ser292del)	COSMIC
17	g.7673712C>A	CA397836310	TP53	c.908G>T (p.Ser303Ile) c.512G>T (p.Ser171Ile) c.629G>T (p.Ser210Ile) c.887G>T (p.Ser296Ile) c.782+469G>T (n.782+469G>T) c.791G>T (p.Ser264Ile) c.431G>T (p.Ser144Ile) c.875G>T (p.Ser292Ile)	dbSNP
17	g.7673712C=	CA2245948500	TP53	c.908G= (p.Ser303=) c.512G= (p.Ser171=) c.629G= (p.Ser210=) c.887G= (p.Ser296=) c.782+469G= (n.782+469G=) c.791G= (p.Ser264=) c.431G= (p.Ser144=) c.875G= (p.Ser292=)
17	g.7673712C>G	CA397836312	TP53	c.908G>C (p.Ser303Thr) c.512G>C (p.Ser171Thr) c.629G>C (p.Ser210Thr) c.887G>C (p.Ser296Thr) c.782+469G>C (n.782+469G>C) c.791G>C (p.Ser264Thr) c.431G>C (p.Ser144Thr) c.875G>C (p.Ser292Thr)	dbSNP COSMIC
17	g.7673712C>T	CA10580912	TP53	c.908G>A (p.Ser303Asn) c.512G>A (p.Ser171Asn) c.629G>A (p.Ser210Asn) c.887G>A (p.Ser296Asn) c.782+469G>A (n.782+469G>A) c.791G>A (p.Ser264Asn) c.431G>A (p.Ser144Asn) c.875G>A (p.Ser292Asn)	ClinVar dbSNP COSMIC
17	g.7673712_7673713insCCCC	CA913190579	TP53	c.908_909insGGGG (p.Ser303ArgfsTer4) c.512_513insGGGG (p.Ser171ArgfsTer4) c.629_630insGGGG (p.Ser210ArgfsTer4) c.887_888insGGGG (p.Ser296ArgfsTer4) c.782+469_782+470insGGGG (n.782+469_782+470insGGGG) c.791_792insGGGG (p.Ser264ArgfsTer4) c.431_432insGGGG (p.Ser144ArgfsTer4) c.875_876insGGGG (p.Ser292ArgfsTer4)	ClinVar dbSNP
17	g.7673712_7673716del	CA645587423	TP53	c.904_908del (p.Gly302HisfsTer2) c.508_512del (p.Gly170HisfsTer2) c.625_629del (p.Gly209HisfsTer2) c.883_887del (p.Gly295HisfsTer2) c.782+465_782+469del (n.782+465_782+469del) c.787_791del (p.Gly263HisfsTer2) c.427_431del (p.Gly143HisfsTer2) c.871_875del (p.Gly291HisfsTer2)	COSMIC
17	g.7673714_7673717dup	CA2825002635	TP53	c.905_908dup (p.Ser303ArgfsTer4) c.509_512dup (p.Ser171ArgfsTer4) c.626_629dup (p.Ser210ArgfsTer4) c.884_887dup (p.Ser296ArgfsTer4) c.782+466_782+469dup (n.782+466_782+469dup) c.788_791dup (p.Ser264ArgfsTer4) c.428_431dup (p.Ser144ArgfsTer4) c.872_875dup (p.Ser292ArgfsTer4)	ClinVar
17	g.7673714_7673717del	CA645587422	TP53	c.905_908del (p.Gly302AlafsTer?) c.509_512del (p.Gly170AlafsTer?) c.626_629del (p.Gly209AlafsTer?) c.884_887del (p.Gly295AlafsTer?) c.782+466_782+469del (n.782+466_782+469del) c.788_791del (p.Gly263AlafsTer?) c.428_431del (p.Gly143AlafsTer?) c.872_875del (p.Gly291AlafsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673713del	CA497715423	TP53	c.907del (p.Ser303AlafsTer?) c.511del (p.Ser171AlafsTer?) c.628del (p.Ser210AlafsTer?) c.886del (p.Ser296AlafsTer?) c.782+468del (n.782+468del) c.790del (p.Ser264AlafsTer?) c.430del (p.Ser144AlafsTer?) c.874del (p.Ser292AlafsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673713T>A	CA397836317	TP53	c.907A>T (p.Ser303Cys) c.511A>T (p.Ser171Cys) c.628A>T (p.Ser210Cys) c.886A>T (p.Ser296Cys) c.782+468A>T (n.782+468A>T) c.790A>T (p.Ser264Cys) c.430A>T (p.Ser144Cys) c.874A>T (p.Ser292Cys)	COSMIC
17	g.7673713T>C	CA000491	TP53	c.907A>G (p.Ser303Gly) c.511A>G (p.Ser171Gly) c.628A>G (p.Ser210Gly) c.886A>G (p.Ser296Gly) c.782+468A>G (n.782+468A>G) c.790A>G (p.Ser264Gly) c.430A>G (p.Ser144Gly) c.874A>G (p.Ser292Gly)	ClinVar dbSNP gnomAD v3 gnomAD v4
17	g.7673713T>G	CA397836320	TP53	c.907A>C (p.Ser303Arg) c.511A>C (p.Ser171Arg) c.628A>C (p.Ser210Arg) c.886A>C (p.Ser296Arg) c.782+468A>C (n.782+468A>C) c.790A>C (p.Ser264Arg) c.430A>C (p.Ser144Arg) c.874A>C (p.Ser292Arg)
17	g.7673713T=	CA2245948516	TP53	c.907A= (p.Ser303=) c.511A= (p.Ser171=) c.628A= (p.Ser210=) c.886A= (p.Ser296=) c.782+468A= (n.782+468A=) c.790A= (p.Ser264=) c.430A= (p.Ser144=) c.874A= (p.Ser292=)
17	g.7673713_7673714delinsTC	CA2245948519	TP53	c.906_907delinsGA (p.Gly302=) c.510_511delinsGA (p.Gly170=) c.627_628delinsGA (p.Gly209=) c.885_886delinsGA (p.Gly295=) c.782+467_782+468delinsGA (n.782+467_782+468delinsGA) c.789_790delinsGA (p.Gly263=) c.429_430delinsGA (p.Gly143=) c.873_874delinsGA (p.Gly291=)
17	g.7673714C>A	CA497715428	TP53	c.906G>T (p.Gly302=) c.510G>T (p.Gly170=) c.627G>T (p.Gly209=) c.885G>T (p.Gly295=) c.782+467G>T (n.782+467G>T) c.789G>T (p.Gly263=) c.429G>T (p.Gly143=) c.873G>T (p.Gly291=)	dbSNP COSMIC
17	g.7673714C>G	CA497715430	TP53	c.906G>C (p.Gly302=) c.510G>C (p.Gly170=) c.627G>C (p.Gly209=) c.885G>C (p.Gly295=) c.782+467G>C (n.782+467G>C) c.789G>C (p.Gly263=) c.429G>C (p.Gly143=) c.873G>C (p.Gly291=)	dbSNP COSMIC
17	g.7673714C>T	CA497715432	TP53	c.906G>A (p.Gly302=) c.510G>A (p.Gly170=) c.627G>A (p.Gly209=) c.885G>A (p.Gly295=) c.782+467G>A (n.782+467G>A) c.789G>A (p.Gly263=) c.429G>A (p.Gly143=) c.873G>A (p.Gly291=)	ClinVar dbSNP
17	g.7673716del	CA000489	TP53	c.906del (p.Ser303AlafsTer?) c.510del (p.Ser171AlafsTer?) c.627del (p.Ser210AlafsTer?) c.885del (p.Ser296AlafsTer?) c.782+467del (n.782+467del) c.789del (p.Ser264AlafsTer?) c.429del (p.Ser144AlafsTer?) c.873del (p.Ser292AlafsTer?)	ClinVar dbSNP COSMIC COSMIC
17	g.7673715C>A	CA397836328	TP53	c.905G>T (p.Gly302Val) c.509G>T (p.Gly170Val) c.626G>T (p.Gly209Val) c.884G>T (p.Gly295Val) c.782+466G>T (n.782+466G>T) c.788G>T (p.Gly263Val) c.428G>T (p.Gly143Val) c.872G>T (p.Gly291Val)	dbSNP
17	g.7673715C=	CA2245948530	TP53	c.905G= (p.Gly302=) c.509G= (p.Gly170=) c.626G= (p.Gly209=) c.884G= (p.Gly295=) c.782+466G= (n.782+466G=) c.788G= (p.Gly263=) c.428G= (p.Gly143=) c.872G= (p.Gly291=)
17	g.7673715C>G	CA397836331	TP53	c.905G>C (p.Gly302Ala) c.509G>C (p.Gly170Ala) c.626G>C (p.Gly209Ala) c.884G>C (p.Gly295Ala) c.782+466G>C (n.782+466G>C) c.788G>C (p.Gly263Ala) c.428G>C (p.Gly143Ala) c.872G>C (p.Gly291Ala)	dbSNP
17	g.7673715C>T	CA16615695	TP53	c.905G>A (p.Gly302Glu) c.509G>A (p.Gly170Glu) c.626G>A (p.Gly209Glu) c.884G>A (p.Gly295Glu) c.782+466G>A (n.782+466G>A) c.788G>A (p.Gly263Glu) c.428G>A (p.Gly143Glu) c.872G>A (p.Gly291Glu)	ClinVar dbSNP COSMIC
17	g.7673716_7673728del	CA645587424	TP53	c.893_905del (p.Glu298GlyfsTer?) c.497_509del (p.Glu166GlyfsTer?) c.614_626del (p.Glu205GlyfsTer?) c.872_884del (p.Glu291GlyfsTer?) c.782+454_782+466del (n.782+454_782+466del) c.776_788del (p.Glu259GlyfsTer?) c.416_428del (p.Glu139GlyfsTer?) c.860_872del (p.Glu287GlyfsTer?)	COSMIC
17	g.7673716C>A	CA397836339	TP53	c.904G>T (p.Gly302Trp) c.508G>T (p.Gly170Trp) c.625G>T (p.Gly209Trp) c.883G>T (p.Gly295Trp) c.782+465G>T (n.782+465G>T) c.787G>T (p.Gly263Trp) c.427G>T (p.Gly143Trp) c.871G>T (p.Gly291Trp)	dbSNP
17	g.7673716C=	CA2245948543	TP53	c.904G= (p.Gly302=) c.508G= (p.Gly170=) c.625G= (p.Gly209=) c.883G= (p.Gly295=) c.782+465G= (n.782+465G=) c.787G= (p.Gly263=) c.427G= (p.Gly143=) c.871G= (p.Gly291=)
17	g.7673716C>G	CA336894	TP53	c.904G>C (p.Gly302Arg) c.508G>C (p.Gly170Arg) c.625G>C (p.Gly209Arg) c.883G>C (p.Gly295Arg) c.782+465G>C (n.782+465G>C) c.787G>C (p.Gly263Arg) c.427G>C (p.Gly143Arg) c.871G>C (p.Gly291Arg)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673716C>T	CA397836336	TP53	c.904G>A (p.Gly302Arg) c.508G>A (p.Gly170Arg) c.625G>A (p.Gly209Arg) c.883G>A (p.Gly295Arg) c.782+465G>A (n.782+465G>A) c.787G>A (p.Gly263Arg) c.427G>A (p.Gly143Arg) c.871G>A (p.Gly291Arg)	ClinVar dbSNP gnomAD v4
17	g.7673716_7673717insAC	CA645587426	TP53	c.904_905insTG (p.Gly302ValfsTer?) c.508_509insTG (p.Gly170ValfsTer?) c.625_626insTG (p.Gly209ValfsTer?) c.883_884insTG (p.Gly295ValfsTer?) c.782+465_782+466insTG (n.782+465_782+466insTG) c.787_788insTG (p.Gly263ValfsTer?) c.427_428insTG (p.Gly143ValfsTer?) c.871_872insTG (p.Gly291ValfsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673717_7673728del	CA645587425	TP53	c.893_904del (p.Glu298_Pro301del) c.497_508del (p.Glu166_Pro169del) c.614_625del (p.Glu205_Pro208del) c.872_883del (p.Glu291_Pro294del) c.782+454_782+465del (n.782+454_782+465del) c.776_787del (p.Glu259_Pro262del) c.416_427del (p.Glu139_Pro142del) c.860_871del (p.Glu287_Pro290del)	COSMIC
17	g.7673718_7673739del	CA2695224219	TP53	c.883_904del (p.Pro295GlyfsTer?) c.487_508del (p.Pro163GlyfsTer?) c.604_625del (p.Pro202GlyfsTer?) c.862_883del (p.Pro288GlyfsTer?) c.782+444_782+465del (n.782+444_782+465del) c.766_787del (p.Pro256GlyfsTer?) c.406_427del (p.Pro136GlyfsTer?) c.850_871del (p.Pro284GlyfsTer?)
17	g.7673717del	CA645587427	TP53	c.903del (p.Ser303AlafsTer?) c.507del (p.Ser171AlafsTer?) c.624del (p.Ser210AlafsTer?) c.882del (p.Ser296AlafsTer?) c.782+464del (n.782+464del) c.786del (p.Ser264AlafsTer?) c.426del (p.Ser144AlafsTer?) c.870del (p.Ser292AlafsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673717T>A	CA497715457	TP53	c.903A>T (p.Pro301=) c.507A>T (p.Pro169=) c.624A>T (p.Pro208=) c.882A>T (p.Pro294=) c.782+464A>T (n.782+464A>T) c.786A>T (p.Pro262=) c.426A>T (p.Pro142=) c.870A>T (p.Pro290=)
17	g.7673717T>C	CA000488	TP53	c.903A>G (p.Pro301=) c.507A>G (p.Pro169=) c.624A>G (p.Pro208=) c.882A>G (p.Pro294=) c.782+464A>G (n.782+464A>G) c.786A>G (p.Pro262=) c.426A>G (p.Pro142=) c.870A>G (p.Pro290=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673717T>G	CA497715458	TP53	c.903A>C (p.Pro301=) c.507A>C (p.Pro169=) c.624A>C (p.Pro208=) c.882A>C (p.Pro294=) c.782+464A>C (n.782+464A>C) c.786A>C (p.Pro262=) c.426A>C (p.Pro142=) c.870A>C (p.Pro290=)
17	g.7673717T=	CA2245948548	TP53	c.903A= (p.Pro301=) c.507A= (p.Pro169=) c.624A= (p.Pro208=) c.882A= (p.Pro294=) c.782+464A= (n.782+464A=) c.786A= (p.Pro262=) c.426A= (p.Pro142=) c.870A= (p.Pro290=)
17	g.7673717_7673718delinsTG	CA2245948550	TP53	c.902_903delinsCA (p.Pro301=) c.506_507delinsCA (p.Pro169=) c.623_624delinsCA (p.Pro208=) c.881_882delinsCA (p.Pro294=) c.782+463_782+464delinsCA (n.782+463_782+464delinsCA) c.785_786delinsCA (p.Pro262=) c.425_426delinsCA (p.Pro142=) c.869_870delinsCA (p.Pro290=)
17	g.7673717_7673718insC	CA645587430	TP53	c.902_903insG (p.Gly302ArgfsTer4) c.506_507insG (p.Gly170ArgfsTer4) c.623_624insG (p.Gly209ArgfsTer4) c.881_882insG (p.Gly295ArgfsTer4) c.782+463_782+464insG (n.782+463_782+464insG) c.785_786insG (p.Gly263ArgfsTer4) c.425_426insG (p.Gly143ArgfsTer4) c.869_870insG (p.Gly291ArgfsTer4)	COSMIC
17	g.7673718G>A	CA397836344	TP53	c.902C>T (p.Pro301Leu) c.506C>T (p.Pro169Leu) c.623C>T (p.Pro208Leu) c.881C>T (p.Pro294Leu) c.782+463C>T (n.782+463C>T) c.785C>T (p.Pro262Leu) c.425C>T (p.Pro142Leu) c.869C>T (p.Pro290Leu)	ClinVar dbSNP COSMIC
17	g.7673718G>C	CA397836347	TP53	c.902C>G (p.Pro301Arg) c.506C>G (p.Pro169Arg) c.623C>G (p.Pro208Arg) c.881C>G (p.Pro294Arg) c.782+463C>G (n.782+463C>G) c.785C>G (p.Pro262Arg) c.425C>G (p.Pro142Arg) c.869C>G (p.Pro290Arg)
17	g.7673718G=	CA2245948580	TP53	c.902C= (p.Pro301=) c.506C= (p.Pro169=) c.623C= (p.Pro208=) c.881C= (p.Pro294=) c.782+463C= (n.782+463C=) c.785C= (p.Pro262=) c.425C= (p.Pro142=) c.869C= (p.Pro290=)
17	g.7673718G>T	CA397836350	TP53	c.902C>A (p.Pro301Gln) c.506C>A (p.Pro169Gln) c.623C>A (p.Pro208Gln) c.881C>A (p.Pro294Gln) c.782+463C>A (n.782+463C>A) c.785C>A (p.Pro262Gln) c.425C>A (p.Pro142Gln) c.869C>A (p.Pro290Gln)	dbSNP COSMIC
17	g.7673722dup	CA497715472	TP53	c.902dup (p.Gly302ArgfsTer4) c.506dup (p.Gly170ArgfsTer4) c.623dup (p.Gly209ArgfsTer4) c.881dup (p.Gly295ArgfsTer4) c.782+463dup (n.782+463dup) c.785dup (p.Gly263ArgfsTer4) c.425dup (p.Gly143ArgfsTer4) c.869dup (p.Gly291ArgfsTer4)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673721_7673722dup	CA915949521	TP53	c.901_902dup (p.Gly302GlnfsTer?) c.505_506dup (p.Gly170GlnfsTer?) c.622_623dup (p.Gly209GlnfsTer?) c.880_881dup (p.Gly295GlnfsTer?) c.782+462_782+463dup (n.782+462_782+463dup) c.784_785dup (p.Gly263GlnfsTer?) c.424_425dup (p.Gly143GlnfsTer?) c.868_869dup (p.Gly291GlnfsTer?)	ClinVar dbSNP
17	g.7673722del	CA10580913	TP53	c.902del (p.Pro301GlnfsTer?) c.506del (p.Pro169GlnfsTer?) c.623del (p.Pro208GlnfsTer?) c.881del (p.Pro294GlnfsTer?) c.782+463del (n.782+463del) c.785del (p.Pro262GlnfsTer?) c.425del (p.Pro142GlnfsTer?) c.869del (p.Pro290GlnfsTer?)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673721_7673722del	CA645587429	TP53	c.901_902del (p.Pro301ArgfsTer4) c.505_506del (p.Pro169ArgfsTer4) c.622_623del (p.Pro208ArgfsTer4) c.880_881del (p.Pro294ArgfsTer4) c.782+462_782+463del (n.782+462_782+463del) c.784_785del (p.Pro262ArgfsTer4) c.424_425del (p.Pro142ArgfsTer4) c.868_869del (p.Pro290ArgfsTer4)	COSMIC
17	g.7673719_7673722del	CA645587428	TP53	c.899_902del (p.Pro300GlnfsTer?) c.503_506del (p.Pro168GlnfsTer?) c.620_623del (p.Pro207GlnfsTer?) c.878_881del (p.Pro293GlnfsTer?) c.782+460_782+463del (n.782+460_782+463del) c.782_785del (p.Pro261GlnfsTer?) c.422_425del (p.Pro141GlnfsTer?) c.866_869del (p.Pro289GlnfsTer?)	COSMIC
17	g.7673719G>A	CA397836354	TP53	c.901C>T (p.Pro301Ser) c.505C>T (p.Pro169Ser) c.622C>T (p.Pro208Ser) c.880C>T (p.Pro294Ser) c.782+462C>T (n.782+462C>T) c.784C>T (p.Pro262Ser) c.424C>T (p.Pro142Ser) c.868C>T (p.Pro290Ser)	ClinVar dbSNP COSMIC
17	g.7673719G>C	CA397836355	TP53	c.901C>G (p.Pro301Ala) c.505C>G (p.Pro169Ala) c.622C>G (p.Pro208Ala) c.880C>G (p.Pro294Ala) c.782+462C>G (n.782+462C>G) c.784C>G (p.Pro262Ala) c.424C>G (p.Pro142Ala) c.868C>G (p.Pro290Ala)	ClinVar dbSNP COSMIC
17	g.7673719G>T	CA397836363	TP53	c.901C>A (p.Pro301Thr) c.505C>A (p.Pro169Thr) c.622C>A (p.Pro208Thr) c.880C>A (p.Pro294Thr) c.782+462C>A (n.782+462C>A) c.784C>A (p.Pro262Thr) c.424C>A (p.Pro142Thr) c.868C>A (p.Pro290Thr)	dbSNP COSMIC
17	g.7673720G>A	CA001360	TP53	c.900C>T (p.Pro300=) c.504C>T (p.Pro168=) c.621C>T (p.Pro207=) c.879C>T (p.Pro293=) c.782+461C>T (n.782+461C>T) c.783C>T (p.Pro261=) c.423C>T (p.Pro141=) c.867C>T (p.Pro289=)	ClinVar dbSNP ExAC gnomAD v2
17	g.7673720G>C	CA16608663	TP53	c.900C>G (p.Pro300=) c.504C>G (p.Pro168=) c.621C>G (p.Pro207=) c.879C>G (p.Pro293=) c.782+461C>G (n.782+461C>G) c.783C>G (p.Pro261=) c.423C>G (p.Pro141=) c.867C>G (p.Pro289=)	ClinVar dbSNP
17	g.7673720G=	CA2245948592	TP53	c.900C= (p.Pro300=) c.504C= (p.Pro168=) c.621C= (p.Pro207=) c.879C= (p.Pro293=) c.782+461C= (n.782+461C=) c.783C= (p.Pro261=) c.423C= (p.Pro141=) c.867C= (p.Pro289=)
17	g.7673720G>T	CA497715485	TP53	c.900C>A (p.Pro300=) c.504C>A (p.Pro168=) c.621C>A (p.Pro207=) c.879C>A (p.Pro293=) c.782+461C>A (n.782+461C>A) c.783C>A (p.Pro261=) c.423C>A (p.Pro141=) c.867C>A (p.Pro289=)	dbSNP COSMIC
17	g.7673721G>A	CA287486577	TP53	c.899C>T (p.Pro300Leu) c.503C>T (p.Pro168Leu) c.620C>T (p.Pro207Leu) c.878C>T (p.Pro293Leu) c.782+460C>T (n.782+460C>T) c.782C>T (p.Pro261Leu) c.422C>T (p.Pro141Leu) c.866C>T (p.Pro289Leu)	ClinVar dbSNP COSMIC
17	g.7673721G>C	CA397836373	TP53	c.899C>G (p.Pro300Arg) c.503C>G (p.Pro168Arg) c.620C>G (p.Pro207Arg) c.878C>G (p.Pro293Arg) c.782+460C>G (n.782+460C>G) c.782C>G (p.Pro261Arg) c.422C>G (p.Pro141Arg) c.866C>G (p.Pro289Arg)	dbSNP COSMIC
17	g.7673721G=	CA2245948607	TP53	c.899C= (p.Pro300=) c.503C= (p.Pro168=) c.620C= (p.Pro207=) c.878C= (p.Pro293=) c.782+460C= (n.782+460C=) c.782C= (p.Pro261=) c.422C= (p.Pro141=) c.866C= (p.Pro289=)
17	g.7673721G>T	CA397836370	TP53	c.899C>A (p.Pro300His) c.503C>A (p.Pro168His) c.620C>A (p.Pro207His) c.878C>A (p.Pro293His) c.782+460C>A (n.782+460C>A) c.782C>A (p.Pro261His) c.422C>A (p.Pro141His) c.866C>A (p.Pro289His)	dbSNP
17	g.7673722_7673725dup	CA913184716	TP53	c.896_899dup (p.Pro301AlafsTer6) c.500_503dup (p.Pro169AlafsTer6) c.617_620dup (p.Pro208AlafsTer6) c.875_878dup (p.Pro294AlafsTer6) c.782+457_782+460dup (n.782+457_782+460dup) c.779_782dup (p.Pro262AlafsTer6) c.419_422dup (p.Pro142AlafsTer6) c.863_866dup (p.Pro290AlafsTer6)
17	g.7673722_7673725del	CA2825002636	TP53	c.896_899del (p.Leu299ProfsTer?) c.500_503del (p.Leu167ProfsTer?) c.617_620del (p.Leu206ProfsTer?) c.875_878del (p.Leu292ProfsTer?) c.782+457_782+460del (n.782+457_782+460del) c.779_782del (p.Leu260ProfsTer?) c.419_422del (p.Leu140ProfsTer?) c.863_866del (p.Leu288ProfsTer?)	ClinVar
17	g.7673722G>A	CA397836387	TP53	c.898C>T (p.Pro300Ser) c.502C>T (p.Pro168Ser) c.619C>T (p.Pro207Ser) c.877C>T (p.Pro293Ser) c.782+459C>T (n.782+459C>T) c.781C>T (p.Pro261Ser) c.421C>T (p.Pro141Ser) c.865C>T (p.Pro289Ser)	dbSNP COSMIC
17	g.7673722G>C	CA397836389	TP53	c.898C>G (p.Pro300Ala) c.502C>G (p.Pro168Ala) c.619C>G (p.Pro207Ala) c.877C>G (p.Pro293Ala) c.782+459C>G (n.782+459C>G) c.781C>G (p.Pro261Ala) c.421C>G (p.Pro141Ala) c.865C>G (p.Pro289Ala)	dbSNP COSMIC
17	g.7673722G>T	CA397836392	TP53	c.898C>A (p.Pro300Thr) c.502C>A (p.Pro168Thr) c.619C>A (p.Pro207Thr) c.877C>A (p.Pro293Thr) c.782+459C>A (n.782+459C>A) c.781C>A (p.Pro261Thr) c.421C>A (p.Pro141Thr) c.865C>A (p.Pro289Thr)	dbSNP
17	g.7673722_7673723insT	CA2825002637	TP53	c.897_898insA (p.Pro300ThrfsTer6) c.501_502insA (p.Pro168ThrfsTer6) c.618_619insA (p.Pro207ThrfsTer6) c.876_877insA (p.Pro293ThrfsTer6) c.782+458_782+459insA (n.782+458_782+459insA) c.780_781insA (p.Pro261ThrfsTer6) c.420_421insA (p.Pro141ThrfsTer6) c.864_865insA (p.Pro289ThrfsTer6)	ClinVar
17	g.7673723C>A	CA497715515	TP53	c.897G>T (p.Leu299=) c.501G>T (p.Leu167=) c.618G>T (p.Leu206=) c.876G>T (p.Leu292=) c.782+458G>T (n.782+458G>T) c.780G>T (p.Leu260=) c.420G>T (p.Leu140=) c.864G>T (p.Leu288=)	ClinVar dbSNP gnomAD v4 COSMIC
17	g.7673723C>G	CA497715510	TP53	c.897G>C (p.Leu299=) c.501G>C (p.Leu167=) c.618G>C (p.Leu206=) c.876G>C (p.Leu292=) c.782+458G>C (n.782+458G>C) c.780G>C (p.Leu260=) c.420G>C (p.Leu140=) c.864G>C (p.Leu288=)	dbSNP
17	g.7673723C>T	CA497715514	TP53	c.897G>A (p.Leu299=) c.501G>A (p.Leu167=) c.618G>A (p.Leu206=) c.876G>A (p.Leu292=) c.782+458G>A (n.782+458G>A) c.780G>A (p.Leu260=) c.420G>A (p.Leu140=) c.864G>A (p.Leu288=)	ClinVar dbSNP
17	g.7673724A>C	CA397836395	TP53	c.896T>G (p.Leu299Arg) c.500T>G (p.Leu167Arg) c.617T>G (p.Leu206Arg) c.875T>G (p.Leu292Arg) c.782+457T>G (n.782+457T>G) c.779T>G (p.Leu260Arg) c.419T>G (p.Leu140Arg) c.863T>G (p.Leu288Arg)
17	g.7673724A>G	CA397836397	TP53	c.896T>C (p.Leu299Pro) c.500T>C (p.Leu167Pro) c.617T>C (p.Leu206Pro) c.875T>C (p.Leu292Pro) c.782+457T>C (n.782+457T>C) c.779T>C (p.Leu260Pro) c.419T>C (p.Leu140Pro) c.863T>C (p.Leu288Pro)	ClinVar dbSNP COSMIC
17	g.7673724A>T	CA397836400	TP53	c.896T>A (p.Leu299Gln) c.500T>A (p.Leu167Gln) c.617T>A (p.Leu206Gln) c.875T>A (p.Leu292Gln) c.782+457T>A (n.782+457T>A) c.779T>A (p.Leu260Gln) c.419T>A (p.Leu140Gln) c.863T>A (p.Leu288Gln)
17	g.7673725del	CA497715527	TP53	c.895del (p.Leu299CysfsTer?) c.499del (p.Leu167CysfsTer?) c.616del (p.Leu206CysfsTer?) c.874del (p.Leu292CysfsTer?) c.782+456del (n.782+456del) c.778del (p.Leu260CysfsTer?) c.418del (p.Leu140CysfsTer?) c.862del (p.Leu288CysfsTer?)	COSMIC
17	g.7673725G>A	CA001368	TP53	c.895C>T (p.Leu299=) c.499C>T (p.Leu167=) c.616C>T (p.Leu206=) c.874C>T (p.Leu292=) c.782+456C>T (n.782+456C>T) c.778C>T (p.Leu260=) c.418C>T (p.Leu140=) c.862C>T (p.Leu288=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673725G>C	CA397836405	TP53	c.895C>G (p.Leu299Val) c.499C>G (p.Leu167Val) c.616C>G (p.Leu206Val) c.874C>G (p.Leu292Val) c.782+456C>G (n.782+456C>G) c.778C>G (p.Leu260Val) c.418C>G (p.Leu140Val) c.862C>G (p.Leu288Val)	dbSNP COSMIC
17	g.7673725G=	CA2245948615	TP53	c.895C= (p.Leu299=) c.499C= (p.Leu167=) c.616C= (p.Leu206=) c.874C= (p.Leu292=) c.782+456C= (n.782+456C=) c.778C= (p.Leu260=) c.418C= (p.Leu140=) c.862C= (p.Leu288=)
17	g.7673725G>T	CA397836407	TP53	c.895C>A (p.Leu299Met) c.499C>A (p.Leu167Met) c.616C>A (p.Leu206Met) c.874C>A (p.Leu292Met) c.782+456C>A (n.782+456C>A) c.778C>A (p.Leu260Met) c.418C>A (p.Leu140Met) c.862C>A (p.Leu288Met)	dbSNP
17	g.7673726_7673729del	CA2573051266	TP53	c.892_895del (p.Glu298CysfsTer?) c.496_499del (p.Glu166CysfsTer?) c.613_616del (p.Glu205CysfsTer?) c.871_874del (p.Glu291CysfsTer?) c.782+453_782+456del (n.782+453_782+456del) c.775_778del (p.Glu259CysfsTer?) c.415_418del (p.Glu139CysfsTer?) c.859_862del (p.Glu287CysfsTer?)
17	g.7673726del	CA497715532	TP53	c.894del (p.Glu298AspfsTer?) c.498del (p.Glu166AspfsTer?) c.615del (p.Glu205AspfsTer?) c.873del (p.Glu291AspfsTer?) c.782+455del (n.782+455del) c.777del (p.Glu259AspfsTer?) c.417del (p.Glu139AspfsTer?) c.861del (p.Glu287AspfsTer?)	COSMIC
17	g.7673726C>A	CA397836413	TP53	c.894G>T (p.Glu298Asp) c.498G>T (p.Glu166Asp) c.615G>T (p.Glu205Asp) c.873G>T (p.Glu291Asp) c.782+455G>T (n.782+455G>T) c.777G>T (p.Glu259Asp) c.417G>T (p.Glu139Asp) c.861G>T (p.Glu287Asp)	dbSNP
17	g.7673726C=	CA2245948627	TP53	c.894G= (p.Glu298=) c.498G= (p.Glu166=) c.615G= (p.Glu205=) c.873G= (p.Glu291=) c.782+455G= (n.782+455G=) c.777G= (p.Glu259=) c.417G= (p.Glu139=) c.861G= (p.Glu287=)
17	g.7673726C>G	CA397836416	TP53	c.894G>C (p.Glu298Asp) c.498G>C (p.Glu166Asp) c.615G>C (p.Glu205Asp) c.873G>C (p.Glu291Asp) c.782+455G>C (n.782+455G>C) c.777G>C (p.Glu259Asp) c.417G>C (p.Glu139Asp) c.861G>C (p.Glu287Asp)	ClinVar dbSNP COSMIC
17	g.7673726C>T	CA001380	TP53	c.894G>A (p.Glu298=) c.498G>A (p.Glu166=) c.615G>A (p.Glu205=) c.873G>A (p.Glu291=) c.782+455G>A (n.782+455G>A) c.777G>A (p.Glu259=) c.417G>A (p.Glu139=) c.861G>A (p.Glu287=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17	g.7673727_7673728dup	CA8354861	TP53	c.893_894dup (p.Leu299SerfsTer?) c.497_498dup (p.Leu167SerfsTer?) c.614_615dup (p.Leu206SerfsTer?) c.872_873dup (p.Leu292SerfsTer?) c.782+454_782+455dup (n.782+454_782+455dup) c.776_777dup (p.Leu260SerfsTer?) c.416_417dup (p.Leu140SerfsTer?) c.860_861dup (p.Leu288SerfsTer?)	dbSNP ExAC gnomAD v2
17	g.7673727T>A	CA397836424	TP53	c.893A>T (p.Glu298Val) c.497A>T (p.Glu166Val) c.614A>T (p.Glu205Val) c.872A>T (p.Glu291Val) c.782+454A>T (n.782+454A>T) c.776A>T (p.Glu259Val) c.416A>T (p.Glu139Val) c.860A>T (p.Glu287Val)	dbSNP COSMIC
17	g.7673727T>C	CA397836427	TP53	c.893A>G (p.Glu298Gly) c.497A>G (p.Glu166Gly) c.614A>G (p.Glu205Gly) c.872A>G (p.Glu291Gly) c.782+454A>G (n.782+454A>G) c.776A>G (p.Glu259Gly) c.416A>G (p.Glu139Gly) c.860A>G (p.Glu287Gly)	ClinVar dbSNP
17	g.7673727T>G	CA397836421	TP53	c.893A>C (p.Glu298Ala) c.497A>C (p.Glu166Ala) c.614A>C (p.Glu205Ala) c.872A>C (p.Glu291Ala) c.782+454A>C (n.782+454A>C) c.776A>C (p.Glu259Ala) c.416A>C (p.Glu139Ala) c.860A>C (p.Glu287Ala)	ClinVar COSMIC
17	g.7673727T=	CA2245948639	TP53	c.893A= (p.Glu298=) c.497A= (p.Glu166=) c.614A= (p.Glu205=) c.872A= (p.Glu291=) c.782+454A= (n.782+454A=) c.776A= (p.Glu259=) c.416A= (p.Glu139=) c.860A= (p.Glu287=)
17	g.7673727_7673728delinsTC	CA2245948634	TP53	c.892_893delinsGA (p.Glu298=) c.496_497delinsGA (p.Glu166=) c.613_614delinsGA (p.Glu205=) c.871_872delinsGA (p.Glu291=) c.782+453_782+454delinsGA (n.782+453_782+454delinsGA) c.775_776delinsGA (p.Glu259=) c.415_416delinsGA (p.Glu139=) c.859_860delinsGA (p.Glu287=)
17	g.7673727_7673732delinsTCGTGG	CA2245948644	TP53	c.888_893delinsCCACGA (p.His296=) c.492_497delinsCCACGA (p.His164=) c.609_614delinsCCACGA (p.His203=) c.867_872delinsCCACGA (p.His289=) c.782+449_782+454delinsCCACGA (n.782+449_782+454delinsCCACGA) c.771_776delinsCCACGA (p.His257=) c.411_416delinsCCACGA (p.His137=) c.855_860delinsCCACGA (p.His285=)
17	g.7673728del	CA1139665115	TP53	c.892del (p.Glu298SerfsTer?) c.496del (p.Glu166SerfsTer?) c.613del (p.Glu205SerfsTer?) c.871del (p.Glu291SerfsTer?) c.782+453del (n.782+453del) c.775del (p.Glu259SerfsTer?) c.415del (p.Glu139SerfsTer?) c.859del (p.Glu287SerfsTer?)	ClinVar dbSNP
17	g.7673728C>A	CA000484	TP53	c.892G>T (p.Glu298Ter) c.496G>T (p.Glu166Ter) c.613G>T (p.Glu205Ter) c.871G>T (p.Glu291Ter) c.782+453G>T (n.782+453G>T) c.775G>T (p.Glu259Ter) c.415G>T (p.Glu139Ter) c.859G>T (p.Glu287Ter)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673728C=	CA2245948671	TP53	c.892G= (p.Glu298=) c.496G= (p.Glu166=) c.613G= (p.Glu205=) c.871G= (p.Glu291=) c.782+453G= (n.782+453G=) c.775G= (p.Glu259=) c.415G= (p.Glu139=) c.859G= (p.Glu287=)
17	g.7673728C>G	CA397836431	TP53	c.892G>C (p.Glu298Gln) c.496G>C (p.Glu166Gln) c.613G>C (p.Glu205Gln) c.871G>C (p.Glu291Gln) c.782+453G>C (n.782+453G>C) c.775G>C (p.Glu259Gln) c.415G>C (p.Glu139Gln) c.859G>C (p.Glu287Gln)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673728C>T	CA000483	TP53	c.892G>A (p.Glu298Lys) c.496G>A (p.Glu166Lys) c.613G>A (p.Glu205Lys) c.871G>A (p.Glu291Lys) c.782+453G>A (n.782+453G>A) c.775G>A (p.Glu259Lys) c.415G>A (p.Glu139Lys) c.859G>A (p.Glu287Lys)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673728delinsAAA	CA2695224220	TP53	c.892delinsTTT (p.Glu298PhefsTer?) c.496delinsTTT (p.Glu166PhefsTer?) c.613delinsTTT (p.Glu205PhefsTer?) c.871delinsTTT (p.Glu291PhefsTer?) c.782+453delinsTTT (n.782+453delinsTTT) c.775delinsTTT (p.Glu259PhefsTer?) c.415delinsTTT (p.Glu139PhefsTer?) c.859delinsTTT (p.Glu287PhefsTer?)
17	g.7673728_7673732del	CA913190580	TP53	c.888_892del (p.His296GlnfsTer8) c.492_496del (p.His164GlnfsTer8) c.609_613del (p.His203GlnfsTer8) c.867_871del (p.His289GlnfsTer8) c.782+449_782+453del (n.782+449_782+453del) c.771_775del (p.His257GlnfsTer8) c.411_415del (p.His137GlnfsTer8) c.855_859del (p.His285GlnfsTer8)	ClinVar dbSNP
17	g.7673728_7673729insT	CA2825002638	TP53	c.891_892insA (p.Glu298ArgfsTer8) c.495_496insA (p.Glu166ArgfsTer8) c.612_613insA (p.Glu205ArgfsTer8) c.870_871insA (p.Glu291ArgfsTer8) c.782+452_782+453insA (n.782+452_782+453insA) c.774_775insA (p.Glu259ArgfsTer8) c.414_415insA (p.Glu139ArgfsTer8) c.858_859insA (p.Glu287ArgfsTer8)	ClinVar
17	g.7673729del	CA2576230622	TP53	c.891del (p.His297GlnfsTer?) c.495del (p.His165GlnfsTer?) c.612del (p.His204GlnfsTer?) c.870del (p.His290GlnfsTer?) c.782+452del (n.782+452del) c.774del (p.His258GlnfsTer?) c.414del (p.His138GlnfsTer?) c.858del (p.His286GlnfsTer?)
17	g.7673729G>A	CA000481	TP53	c.891C>T (p.His297=) c.495C>T (p.His165=) c.612C>T (p.His204=) c.870C>T (p.His290=) c.782+452C>T (n.782+452C>T) c.774C>T (p.His258=) c.414C>T (p.His138=) c.858C>T (p.His286=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17	g.7673729G>C	CA397836436	TP53	c.891C>G (p.His297Gln) c.495C>G (p.His165Gln) c.612C>G (p.His204Gln) c.870C>G (p.His290Gln) c.782+452C>G (n.782+452C>G) c.774C>G (p.His258Gln) c.414C>G (p.His138Gln) c.858C>G (p.His286Gln)	ClinVar dbSNP
17	g.7673729G=	CA2245948694	TP53	c.891C= (p.His297=) c.495C= (p.His165=) c.612C= (p.His204=) c.870C= (p.His290=) c.782+452C= (n.782+452C=) c.774C= (p.His258=) c.414C= (p.His138=) c.858C= (p.His286=)
17	g.7673729G>T	CA397836439	TP53	c.891C>A (p.His297Gln) c.495C>A (p.His165Gln) c.612C>A (p.His204Gln) c.870C>A (p.His290Gln) c.782+452C>A (n.782+452C>A) c.774C>A (p.His258Gln) c.414C>A (p.His138Gln) c.858C>A (p.His286Gln)	ClinVar dbSNP
17	g.7673729dup	CA2573054584	TP53	c.891dup (p.Glu298ArgfsTer8) c.495dup (p.Glu166ArgfsTer8) c.612dup (p.Glu205ArgfsTer8) c.870dup (p.Glu291ArgfsTer8) c.782+452dup (n.782+452dup) c.774dup (p.Glu259ArgfsTer8) c.414dup (p.Glu139ArgfsTer8) c.858dup (p.Glu287ArgfsTer8)	ClinVar dbSNP
17	g.7673730_7673731dup	CA645588302	TP53	c.890_891dup (p.Glu298ThrfsTer?) c.494_495dup (p.Glu166ThrfsTer?) c.611_612dup (p.Glu205ThrfsTer?) c.869_870dup (p.Glu291ThrfsTer?) c.782+451_782+452dup (n.782+451_782+452dup) c.773_774dup (p.Glu259ThrfsTer?) c.413_414dup (p.Glu139ThrfsTer?) c.857_858dup (p.Glu287ThrfsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673730del	CA497715562	TP53	c.890del (p.His297ProfsTer?) c.494del (p.His165ProfsTer?) c.611del (p.His204ProfsTer?) c.869del (p.His290ProfsTer?) c.782+451del (n.782+451del) c.773del (p.His258ProfsTer?) c.413del (p.His138ProfsTer?) c.857del (p.His286ProfsTer?)	ClinVar COSMIC
17	g.7673730T>A	CA397836447	TP53	c.890A>T (p.His297Leu) c.494A>T (p.His165Leu) c.611A>T (p.His204Leu) c.869A>T (p.His290Leu) c.782+451A>T (n.782+451A>T) c.773A>T (p.His258Leu) c.413A>T (p.His138Leu) c.857A>T (p.His286Leu)	dbSNP
17	g.7673730T>C	CA10580914	TP53	c.890A>G (p.His297Arg) c.494A>G (p.His165Arg) c.611A>G (p.His204Arg) c.869A>G (p.His290Arg) c.782+451A>G (n.782+451A>G) c.773A>G (p.His258Arg) c.413A>G (p.His138Arg) c.857A>G (p.His286Arg)	ClinVar dbSNP
17	g.7673730T>G	CA397836444	TP53	c.890A>C (p.His297Pro) c.494A>C (p.His165Pro) c.611A>C (p.His204Pro) c.869A>C (p.His290Pro) c.782+451A>C (n.782+451A>C) c.773A>C (p.His258Pro) c.413A>C (p.His138Pro) c.857A>C (p.His286Pro)	COSMIC
17	g.7673730T=	CA2245948709	TP53	c.890A= (p.His297=) c.494A= (p.His165=) c.611A= (p.His204=) c.869A= (p.His290=) c.782+451A= (n.782+451A=) c.773A= (p.His258=) c.413A= (p.His138=) c.857A= (p.His286=)
17	g.7673732_7673750dup	CA2499224957	TP53	c.872_890dup (p.His297GlnfsTer15) c.476_494dup (p.His165GlnfsTer15) c.593_611dup (p.His204GlnfsTer15) c.851_869dup (p.His290GlnfsTer15) c.782+433_782+451dup (n.782+433_782+451dup) c.755_773dup (p.His258GlnfsTer15) c.395_413dup (p.His138GlnfsTer15) c.839_857dup (p.His286GlnfsTer15)	ClinVar dbSNP
17	g.7673732_7673750del	CA645588303	TP53	c.872_890del (p.Lys291ThrfsTer?) c.476_494del (p.Lys159ThrfsTer?) c.593_611del (p.Lys198ThrfsTer?) c.851_869del (p.Lys284ThrfsTer?) c.782+433_782+451del (n.782+433_782+451del) c.755_773del (p.Lys252ThrfsTer?) c.395_413del (p.Lys132ThrfsTer?) c.839_857del (p.Lys280ThrfsTer?)	COSMIC
17	g.7673730_7673775delinsTGGTGAGGCTCCCCTTTCTTGCGGAGATTCTCTTCCTCTGTGCGCC	CA2245948714	TP53	c.845_890delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg282=) c.449_494delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg150=) c.566_611delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg189=) c.824_869delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg275=) c.782+406_782+451delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (n.782+406_782+451delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA) c.728_773delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg243=) c.368_413delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg123=) c.812_857delinsGGCGCACAGAGGAAGAGAATCTCCGCAAGAAAGGGGAGCCTCACCA (p.Arg271=)
17	g.7673731G>A	CA397836451	TP53	c.889C>T (p.His297Tyr) c.493C>T (p.His165Tyr) c.610C>T (p.His204Tyr) c.868C>T (p.His290Tyr) c.782+450C>T (n.782+450C>T) c.772C>T (p.His258Tyr) c.412C>T (p.His138Tyr) c.856C>T (p.His286Tyr)	ClinVar COSMIC
17	g.7673731G>C	CA397836454	TP53	c.889C>G (p.His297Asp) c.493C>G (p.His165Asp) c.610C>G (p.His204Asp) c.868C>G (p.His290Asp) c.782+450C>G (n.782+450C>G) c.772C>G (p.His258Asp) c.412C>G (p.His138Asp) c.856C>G (p.His286Asp)
17	g.7673731G>T	CA397836457	TP53	c.889C>A (p.His297Asn) c.493C>A (p.His165Asn) c.610C>A (p.His204Asn) c.868C>A (p.His290Asn) c.782+450C>A (n.782+450C>A) c.772C>A (p.His258Asn) c.412C>A (p.His138Asn) c.856C>A (p.His286Asn)	COSMIC
17	g.7673731_7673732delinsAA	CA645588306	TP53	c.888_889delinsTT (p.His297Tyr) c.492_493delinsTT (p.His165Tyr) c.609_610delinsTT (p.His204Tyr) c.867_868delinsTT (p.His290Tyr) c.782+449_782+450delinsTT (n.782+449_782+450delinsTT) c.771_772delinsTT (p.His258Tyr) c.411_412delinsTT (p.His138Tyr) c.855_856delinsTT (p.His286Tyr)	COSMIC
17	g.7673732del	CA645588304	TP53	c.889del (p.His297ThrfsTer?) c.493del (p.His165ThrfsTer?) c.610del (p.His204ThrfsTer?) c.868del (p.His290ThrfsTer?) c.782+450del (n.782+450del) c.772del (p.His258ThrfsTer?) c.412del (p.His138ThrfsTer?) c.856del (p.His286ThrfsTer?)	COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673733_7673737del	CA645588305	TP53	c.885_889del (p.His296ArgfsTer8) c.489_493del (p.His164ArgfsTer8) c.606_610del (p.His203ArgfsTer8) c.864_868del (p.His289ArgfsTer8) c.782+446_782+450del (n.782+446_782+450del) c.768_772del (p.His257ArgfsTer8) c.408_412del (p.His137ArgfsTer8) c.852_856del (p.His285ArgfsTer8)	COSMIC
17	g.7673734_7673778del	CA913190582	TP53	c.845_889del (p.Arg282_His296del) c.449_493del (p.Arg150_His164del) c.566_610del (p.Arg189_His203del) c.824_868del (p.Arg275_His289del) c.782+406_782+450del (n.782+406_782+450del) c.728_772del (p.Arg243_His257del) c.368_412del (p.Arg123_His137del) c.812_856del (p.Arg271_His285del)	ClinVar dbSNP
17	g.7673732G>A	CA001400	TP53	c.888C>T (p.His296=) c.492C>T (p.His164=) c.609C>T (p.His203=) c.867C>T (p.His289=) c.782+449C>T (n.782+449C>T) c.771C>T (p.His257=) c.411C>T (p.His137=) c.855C>T (p.His285=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17	g.7673732G>C	CA397836462	TP53	c.888C>G (p.His296Gln) c.492C>G (p.His164Gln) c.609C>G (p.His203Gln) c.867C>G (p.His289Gln) c.782+449C>G (n.782+449C>G) c.771C>G (p.His257Gln) c.411C>G (p.His137Gln) c.855C>G (p.His285Gln)	dbSNP gnomAD v4 COSMIC
17	g.7673732G=	CA2245948726	TP53	c.888C= (p.His296=) c.492C= (p.His164=) c.609C= (p.His203=) c.867C= (p.His289=) c.782+449C= (n.782+449C=) c.771C= (p.His257=) c.411C= (p.His137=) c.855C= (p.His285=)
17	g.7673732G>T	CA397836469	TP53	c.888C>A (p.His296Gln) c.492C>A (p.His164Gln) c.609C>A (p.His203Gln) c.867C>A (p.His289Gln) c.782+449C>A (n.782+449C>A) c.771C>A (p.His257Gln) c.411C>A (p.His137Gln) c.855C>A (p.His285Gln)	dbSNP
17	g.7673733_7673736dup	CA645588308	TP53	c.885_888dup (p.His297SerfsTer10) c.489_492dup (p.His165SerfsTer10) c.606_609dup (p.His204SerfsTer10) c.864_867dup (p.His290SerfsTer10) c.782+446_782+449dup (n.782+446_782+449dup) c.768_771dup (p.His258SerfsTer10) c.408_411dup (p.His138SerfsTer10) c.852_855dup (p.His286SerfsTer10)	COSMIC COSMIC COSMIC COSMIC
17	g.7673732_7673747del	CA645588307	TP53	c.873_888del (p.Lys291AsnfsTer?) c.477_492del (p.Lys159AsnfsTer?) c.594_609del (p.Lys198AsnfsTer?) c.852_867del (p.Lys284AsnfsTer?) c.782+434_782+449del (n.782+434_782+449del) c.756_771del (p.Lys252AsnfsTer?) c.396_411del (p.Lys132AsnfsTer?) c.840_855del (p.Lys280AsnfsTer?)	COSMIC
17	g.7673733T>A	CA397836474	TP53	c.887A>T (p.His296Leu) c.491A>T (p.His164Leu) c.608A>T (p.His203Leu) c.866A>T (p.His289Leu) c.782+448A>T (n.782+448A>T) c.770A>T (p.His257Leu) c.410A>T (p.His137Leu) c.854A>T (p.His285Leu)	dbSNP COSMIC
17	g.7673733T>C	CA000476	TP53	c.887A>G (p.His296Arg) c.491A>G (p.His164Arg) c.608A>G (p.His203Arg) c.866A>G (p.His289Arg) c.782+448A>G (n.782+448A>G) c.770A>G (p.His257Arg) c.410A>G (p.His137Arg) c.854A>G (p.His285Arg)	ClinVar dbSNP COSMIC
17	g.7673733T>G	CA397836477	TP53	c.887A>C (p.His296Pro) c.491A>C (p.His164Pro) c.608A>C (p.His203Pro) c.866A>C (p.His289Pro) c.782+448A>C (n.782+448A>C) c.770A>C (p.His257Pro) c.410A>C (p.His137Pro) c.854A>C (p.His285Pro)	dbSNP COSMIC
17	g.7673733T=	CA2245948734	TP53	c.887A= (p.His296=) c.491A= (p.His164=) c.608A= (p.His203=) c.866A= (p.His289=) c.782+448A= (n.782+448A=) c.770A= (p.His257=) c.410A= (p.His137=) c.854A= (p.His285=)
17	g.7673734del	CA497715574	TP53	c.886del (p.His296ThrfsTer?) c.490del (p.His164ThrfsTer?) c.607del (p.His203ThrfsTer?) c.865del (p.His289ThrfsTer?) c.782+447del (n.782+447del) c.769del (p.His257ThrfsTer?) c.409del (p.His137ThrfsTer?) c.853del (p.His285ThrfsTer?)	COSMIC
17	g.7673734G>A	CA000474	TP53	c.886C>T (p.His296Tyr) c.490C>T (p.His164Tyr) c.607C>T (p.His203Tyr) c.865C>T (p.His289Tyr) c.782+447C>T (n.782+447C>T) c.769C>T (p.His257Tyr) c.409C>T (p.His137Tyr) c.853C>T (p.His285Tyr)	ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17	g.7673734G>C	CA397836484	TP53	c.886C>G (p.His296Asp) c.490C>G (p.His164Asp) c.607C>G (p.His203Asp) c.865C>G (p.His289Asp) c.782+447C>G (n.782+447C>G) c.769C>G (p.His257Asp) c.409C>G (p.His137Asp) c.853C>G (p.His285Asp)	dbSNP
17	g.7673734G=	CA2245948740	TP53	c.886C= (p.His296=) c.490C= (p.His164=) c.607C= (p.His203=) c.865C= (p.His289=) c.782+447C= (n.782+447C=) c.769C= (p.His257=) c.409C= (p.His137=) c.853C= (p.His285=)
17	g.7673734G>T	CA397836485	TP53	c.886C>A (p.His296Asn) c.490C>A (p.His164Asn) c.607C>A (p.His203Asn) c.865C>A (p.His289Asn) c.782+447C>A (n.782+447C>A) c.769C>A (p.His257Asn) c.409C>A (p.His137Asn) c.853C>A (p.His285Asn)	COSMIC
17	g.7673734_7673737del	CA2733133873	TP53	c.883_886del (p.Pro295ThrfsTer?) c.487_490del (p.Pro163ThrfsTer?) c.604_607del (p.Pro202ThrfsTer?) c.862_865del (p.Pro288ThrfsTer?) c.782+444_782+447del (n.782+444_782+447del) c.766_769del (p.Pro256ThrfsTer?) c.406_409del (p.Pro136ThrfsTer?) c.850_853del (p.Pro284ThrfsTer?)	dbSNP
17	g.7673735A=	CA2245948749	TP53	c.885T= (p.Pro295=) c.489T= (p.Pro163=) c.606T= (p.Pro202=) c.864T= (p.Pro288=) c.782+446T= (n.782+446T=) c.768T= (p.Pro256=) c.408T= (p.Pro136=) c.852T= (p.Pro284=)
17	g.7673735A>C	CA497715580	TP53	c.885T>G (p.Pro295=) c.489T>G (p.Pro163=) c.606T>G (p.Pro202=) c.864T>G (p.Pro288=) c.782+446T>G (n.782+446T>G) c.768T>G (p.Pro256=) c.408T>G (p.Pro136=) c.852T>G (p.Pro284=)
17	g.7673735A>G	CA000472	TP53	c.885T>C (p.Pro295=) c.489T>C (p.Pro163=) c.606T>C (p.Pro202=) c.864T>C (p.Pro288=) c.782+446T>C (n.782+446T>C) c.768T>C (p.Pro256=) c.408T>C (p.Pro136=) c.852T>C (p.Pro284=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673735A>T	CA497715583	TP53	c.885T>A (p.Pro295=) c.489T>A (p.Pro163=) c.606T>A (p.Pro202=) c.864T>A (p.Pro288=) c.782+446T>A (n.782+446T>A) c.768T>A (p.Pro256=) c.408T>A (p.Pro136=) c.852T>A (p.Pro284=)	ClinVar dbSNP
17	g.7673735dup	CA1139768297	TP53	c.885dup (p.His296SerfsTer10) c.489dup (p.His164SerfsTer10) c.606dup (p.His203SerfsTer10) c.864dup (p.His289SerfsTer10) c.782+446dup (n.782+446dup) c.768dup (p.His257SerfsTer10) c.408dup (p.His137SerfsTer10) c.852dup (p.His285SerfsTer10)
17	g.7673736G>A	CA001416	TP53	c.884C>T (p.Pro295Leu) c.488C>T (p.Pro163Leu) c.605C>T (p.Pro202Leu) c.863C>T (p.Pro288Leu) c.782+445C>T (n.782+445C>T) c.767C>T (p.Pro256Leu) c.407C>T (p.Pro136Leu) c.851C>T (p.Pro284Leu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673736G>C	CA397836491	TP53	c.884C>G (p.Pro295Arg) c.488C>G (p.Pro163Arg) c.605C>G (p.Pro202Arg) c.863C>G (p.Pro288Arg) c.782+445C>G (n.782+445C>G) c.767C>G (p.Pro256Arg) c.407C>G (p.Pro136Arg) c.851C>G (p.Pro284Arg)	dbSNP COSMIC
17	g.7673736G=	CA2245948762	TP53	c.884C= (p.Pro295=) c.488C= (p.Pro163=) c.605C= (p.Pro202=) c.863C= (p.Pro288=) c.782+445C= (n.782+445C=) c.767C= (p.Pro256=) c.407C= (p.Pro136=) c.851C= (p.Pro284=)
17	g.7673736G>T	CA397836493	TP53	c.884C>A (p.Pro295His) c.488C>A (p.Pro163His) c.605C>A (p.Pro202His) c.863C>A (p.Pro288His) c.782+445C>A (n.782+445C>A) c.767C>A (p.Pro256His) c.407C>A (p.Pro136His) c.851C>A (p.Pro284His)	dbSNP COSMIC
17	g.7673738_7673753del	CA645588309	TP53	c.869_884del (p.Arg290LeufsTer?) c.473_488del (p.Arg158LeufsTer?) c.590_605del (p.Arg197LeufsTer?) c.848_863del (p.Arg283LeufsTer?) c.782+430_782+445del (n.782+430_782+445del) c.752_767del (p.Arg251LeufsTer?) c.392_407del (p.Arg131LeufsTer?) c.836_851del (p.Arg279LeufsTer?)	COSMIC
17	g.7673737G>A	CA397836496	TP53	c.883C>T (p.Pro295Ser) c.487C>T (p.Pro163Ser) c.604C>T (p.Pro202Ser) c.862C>T (p.Pro288Ser) c.782+444C>T (n.782+444C>T) c.766C>T (p.Pro256Ser) c.406C>T (p.Pro136Ser) c.850C>T (p.Pro284Ser)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673737G>C	CA397836498	TP53	c.883C>G (p.Pro295Ala) c.487C>G (p.Pro163Ala) c.604C>G (p.Pro202Ala) c.862C>G (p.Pro288Ala) c.782+444C>G (n.782+444C>G) c.766C>G (p.Pro256Ala) c.406C>G (p.Pro136Ala) c.850C>G (p.Pro284Ala)	dbSNP COSMIC
17	g.7673737G=	CA2245948771	TP53	c.883C= (p.Pro295=) c.487C= (p.Pro163=) c.604C= (p.Pro202=) c.862C= (p.Pro288=) c.782+444C= (n.782+444C=) c.766C= (p.Pro256=) c.406C= (p.Pro136=) c.850C= (p.Pro284=)
17	g.7673737G>T	CA397836501	TP53	c.883C>A (p.Pro295Thr) c.487C>A (p.Pro163Thr) c.604C>A (p.Pro202Thr) c.862C>A (p.Pro288Thr) c.782+444C>A (n.782+444C>A) c.766C>A (p.Pro256Thr) c.406C>A (p.Pro136Thr) c.850C>A (p.Pro284Thr)	dbSNP
17	g.7673737_7673740dup	CA645588310	TP53	c.880_883dup (p.Pro295ArgfsTer12) c.484_487dup (p.Pro163ArgfsTer12) c.601_604dup (p.Pro202ArgfsTer12) c.859_862dup (p.Pro288ArgfsTer12) c.782+441_782+444dup (n.782+441_782+444dup) c.763_766dup (p.Pro256ArgfsTer12) c.403_406dup (p.Pro136ArgfsTer12) c.847_850dup (p.Pro284ArgfsTer12)	COSMIC
17	g.7673739_7673751dup	CA2635874653	TP53	c.871_883dup (p.Pro295GlnfsTer15) c.475_487dup (p.Pro163GlnfsTer15) c.592_604dup (p.Pro202GlnfsTer15) c.850_862dup (p.Pro288GlnfsTer15) c.782+432_782+444dup (n.782+432_782+444dup) c.754_766dup (p.Pro256GlnfsTer15) c.394_406dup (p.Pro136GlnfsTer15) c.838_850dup (p.Pro284GlnfsTer15)	ClinVar gnomAD v4
17	g.7673738C>A	CA397836504	TP53	c.882G>T (p.Glu294Asp) c.486G>T (p.Glu162Asp) c.603G>T (p.Glu201Asp) c.861G>T (p.Glu287Asp) c.782+443G>T (n.782+443G>T) c.765G>T (p.Glu255Asp) c.405G>T (p.Glu135Asp) c.849G>T (p.Glu283Asp)	COSMIC
17	g.7673738C=	CA2245948775	TP53	c.882G= (p.Glu294=) c.486G= (p.Glu162=) c.603G= (p.Glu201=) c.861G= (p.Glu287=) c.782+443G= (n.782+443G=) c.765G= (p.Glu255=) c.405G= (p.Glu135=) c.849G= (p.Glu283=)
17	g.7673738C>G	CA397836506	TP53	c.882G>C (p.Glu294Asp) c.486G>C (p.Glu162Asp) c.603G>C (p.Glu201Asp) c.861G>C (p.Glu287Asp) c.782+443G>C (n.782+443G>C) c.765G>C (p.Glu255Asp) c.405G>C (p.Glu135Asp) c.849G>C (p.Glu283Asp)	dbSNP gnomAD v2 gnomAD v4
17	g.7673738C>T	CA497715593	TP53	c.882G>A (p.Glu294=) c.486G>A (p.Glu162=) c.603G>A (p.Glu201=) c.861G>A (p.Glu287=) c.782+443G>A (n.782+443G>A) c.765G>A (p.Glu255=) c.405G>A (p.Glu135=) c.849G>A (p.Glu283=)	ClinVar dbSNP COSMIC
17	g.7673739T>A	CA397836514	TP53	c.881A>T (p.Glu294Val) c.485A>T (p.Glu162Val) c.602A>T (p.Glu201Val) c.860A>T (p.Glu287Val) c.782+442A>T (n.782+442A>T) c.764A>T (p.Glu255Val) c.404A>T (p.Glu135Val) c.848A>T (p.Glu283Val)	dbSNP gnomAD v4 COSMIC
17	g.7673739T>C	CA397836512	TP53	c.881A>G (p.Glu294Gly) c.485A>G (p.Glu162Gly) c.602A>G (p.Glu201Gly) c.860A>G (p.Glu287Gly) c.782+442A>G (n.782+442A>G) c.764A>G (p.Glu255Gly) c.404A>G (p.Glu135Gly) c.848A>G (p.Glu283Gly)	COSMIC
17	g.7673739T>G	CA397836510	TP53	c.881A>C (p.Glu294Ala) c.485A>C (p.Glu162Ala) c.602A>C (p.Glu201Ala) c.860A>C (p.Glu287Ala) c.782+442A>C (n.782+442A>C) c.764A>C (p.Glu255Ala) c.404A>C (p.Glu135Ala) c.848A>C (p.Glu283Ala)	ClinVar dbSNP
17	g.7673740C>A	CA16608665	TP53	c.880G>T (p.Glu294Ter) c.484G>T (p.Glu162Ter) c.601G>T (p.Glu201Ter) c.859G>T (p.Glu287Ter) c.782+441G>T (n.782+441G>T) c.763G>T (p.Glu255Ter) c.403G>T (p.Glu135Ter) c.847G>T (p.Glu283Ter)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673740C=	CA2245948782	TP53	c.880G= (p.Glu294=) c.484G= (p.Glu162=) c.601G= (p.Glu201=) c.859G= (p.Glu287=) c.782+441G= (n.782+441G=) c.763G= (p.Glu255=) c.403G= (p.Glu135=) c.847G= (p.Glu283=)
17	g.7673740C>G	CA397836519	TP53	c.880G>C (p.Glu294Gln) c.484G>C (p.Glu162Gln) c.601G>C (p.Glu201Gln) c.859G>C (p.Glu287Gln) c.782+441G>C (n.782+441G>C) c.763G>C (p.Glu255Gln) c.403G>C (p.Glu135Gln) c.847G>C (p.Glu283Gln)	dbSNP COSMIC
17	g.7673740C>T	CA397836516	TP53	c.880G>A (p.Glu294Lys) c.484G>A (p.Glu162Lys) c.601G>A (p.Glu201Lys) c.859G>A (p.Glu287Lys) c.782+441G>A (n.782+441G>A) c.763G>A (p.Glu255Lys) c.403G>A (p.Glu135Lys) c.847G>A (p.Glu283Lys)	ClinVar dbSNP gnomAD v4 COSMIC
17	g.7673740_7673741delinsAA	CA645588311	TP53	c.879_880delinsTT (p.Gly294Ter) c.483_484delinsTT (p.Gly162Ter) c.600_601delinsTT (p.Gly201Ter) c.858_859delinsTT (p.Gly287Ter) c.782+440_782+441delinsTT (n.782+440_782+441delinsTT) c.762_763delinsTT (p.Gly255Ter) c.402_403delinsTT (p.Gly135Ter) c.846_847delinsTT (p.Gly283Ter)	COSMIC
17	g.7673743dup	CA645588312	TP53	c.880dup (p.Glu294GlyfsTer12) c.484dup (p.Glu162GlyfsTer12) c.601dup (p.Glu201GlyfsTer12) c.859dup (p.Glu287GlyfsTer12) c.782+441dup (n.782+441dup) c.763dup (p.Glu255GlyfsTer12) c.403dup (p.Glu135GlyfsTer12) c.847dup (p.Glu283GlyfsTer12)	ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17	g.7673743del	CA497715614	TP53	c.880del (p.Glu294SerfsTer?) c.484del (p.Glu162SerfsTer?) c.601del (p.Glu201SerfsTer?) c.859del (p.Glu287SerfsTer?) c.782+441del (n.782+441del) c.763del (p.Glu255SerfsTer?) c.403del (p.Glu135SerfsTer?) c.847del (p.Glu283SerfsTer?)	ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673742_7673743del	CA645588313	TP53	c.879_880del (p.Glu294AlafsTer11) c.483_484del (p.Glu162AlafsTer11) c.600_601del (p.Glu201AlafsTer11) c.858_859del (p.Glu287AlafsTer11) c.782+440_782+441del (n.782+440_782+441del) c.762_763del (p.Glu255AlafsTer11) c.402_403del (p.Glu135AlafsTer11) c.846_847del (p.Glu283AlafsTer11)	COSMIC COSMIC COSMIC COSMIC
17	g.7673741C>A	CA497715626	TP53	c.879G>T (p.Gly293=) c.483G>T (p.Gly161=) c.600G>T (p.Gly200=) c.858G>T (p.Gly286=) c.782+440G>T (n.782+440G>T) c.762G>T (p.Gly254=) c.402G>T (p.Gly134=) c.846G>T (p.Gly282=)	dbSNP
17	g.7673741C=	CA2245948790	TP53	c.879G= (p.Gly293=) c.483G= (p.Gly161=) c.600G= (p.Gly200=) c.858G= (p.Gly286=) c.782+440G= (n.782+440G=) c.762G= (p.Gly254=) c.402G= (p.Gly134=) c.846G= (p.Gly282=)
17	g.7673741C>G	CA497715622	TP53	c.879G>C (p.Gly293=) c.483G>C (p.Gly161=) c.600G>C (p.Gly200=) c.858G>C (p.Gly286=) c.782+440G>C (n.782+440G>C) c.762G>C (p.Gly254=) c.402G>C (p.Gly134=) c.846G>C (p.Gly282=)	dbSNP COSMIC
17	g.7673741C>T	CA497715623	TP53	c.879G>A (p.Gly293=) c.483G>A (p.Gly161=) c.600G>A (p.Gly200=) c.858G>A (p.Gly286=) c.782+440G>A (n.782+440G>A) c.762G>A (p.Gly254=) c.402G>A (p.Gly134=) c.846G>A (p.Gly282=)	ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17	g.7673742C>A	CA397836521	TP53	c.878G>T (p.Gly293Val) c.482G>T (p.Gly161Val) c.599G>T (p.Gly200Val) c.857G>T (p.Gly286Val) c.782+439G>T (n.782+439G>T) c.761G>T (p.Gly254Val) c.401G>T (p.Gly134Val) c.845G>T (p.Gly282Val)	dbSNP COSMIC
17	g.7673742C>G	CA397836525	TP53	c.878G>C (p.Gly293Ala) c.482G>C (p.Gly161Ala) c.599G>C (p.Gly200Ala) c.857G>C (p.Gly286Ala) c.782+439G>C (n.782+439G>C) c.761G>C (p.Gly254Ala) c.401G>C (p.Gly134Ala) c.845G>C (p.Gly282Ala)	dbSNP COSMIC
17	g.7673742C>T	CA397836523	TP53	c.878G>A (p.Gly293Glu) c.482G>A (p.Gly161Glu) c.599G>A (p.Gly200Glu) c.857G>A (p.Gly286Glu) c.782+439G>A (n.782+439G>A) c.761G>A (p.Gly254Glu) c.401G>A (p.Gly134Glu) c.845G>A (p.Gly282Glu)	dbSNP
17	g.7673742_7673752del	CA645588315	TP53	c.868_878del (p.Arg290GlyfsTer12) c.472_482del (p.Arg158GlyfsTer12) c.589_599del (p.Arg197GlyfsTer12) c.847_857del (p.Arg283GlyfsTer12) c.782+429_782+439del (n.782+429_782+439del) c.751_761del (p.Arg251GlyfsTer12) c.391_401del (p.Arg131GlyfsTer12) c.835_845del (p.Arg279GlyfsTer12)	COSMIC
17	g.7673743_7673772del	CA645588314	TP53	c.849_878del (p.Thr284_Gly293del) c.453_482del (p.Thr152_Gly161del) c.570_599del (p.Thr191_Gly200del) c.828_857del (p.Thr277_Gly286del) c.782+410_782+439del (n.782+410_782+439del) c.732_761del (p.Thr245_Gly254del) c.372_401del (p.Thr125_Gly134del) c.816_845del (p.Thr273_Gly282del)	COSMIC
17	g.7673743C>A	CA000470	TP53	c.877G>T (p.Gly293Trp) c.481G>T (p.Gly161Trp) c.598G>T (p.Gly200Trp) c.856G>T (p.Gly286Trp) c.782+438G>T (n.782+438G>T) c.760G>T (p.Gly254Trp) c.400G>T (p.Gly134Trp) c.844G>T (p.Gly282Trp)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673743C=	CA2245948798	TP53	c.877G= (p.Gly293=) c.481G= (p.Gly161=) c.598G= (p.Gly200=) c.856G= (p.Gly286=) c.782+438G= (n.782+438G=) c.760G= (p.Gly254=) c.400G= (p.Gly134=) c.844G= (p.Gly282=)
17	g.7673743C>G	CA397836528	TP53	c.877G>C (p.Gly293Arg) c.481G>C (p.Gly161Arg) c.598G>C (p.Gly200Arg) c.856G>C (p.Gly286Arg) c.782+438G>C (n.782+438G>C) c.760G>C (p.Gly254Arg) c.400G>C (p.Gly134Arg) c.844G>C (p.Gly282Arg)	ClinVar dbSNP gnomAD v4 COSMIC
17	g.7673743C>T	CA001422	TP53	c.877G>A (p.Gly293Arg) c.481G>A (p.Gly161Arg) c.598G>A (p.Gly200Arg) c.856G>A (p.Gly286Arg) c.782+438G>A (n.782+438G>A) c.760G>A (p.Gly254Arg) c.400G>A (p.Gly134Arg) c.844G>A (p.Gly282Arg)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
17	g.7673743_7673744del	CA645588316	TP53	c.876_877del (p.Glu294AlafsTer11) c.480_481del (p.Glu162AlafsTer11) c.597_598del (p.Glu201AlafsTer11) c.855_856del (p.Glu287AlafsTer11) c.782+437_782+438del (n.782+437_782+438del) c.759_760del (p.Glu255AlafsTer11) c.399_400del (p.Glu135AlafsTer11) c.843_844del (p.Glu283AlafsTer11)	COSMIC COSMIC COSMIC COSMIC
17	g.7673746_7673749del	CA645588317	TP53	c.874_877del (p.Lys292GlyfsTer?) c.478_481del (p.Lys160GlyfsTer?) c.595_598del (p.Lys199GlyfsTer?) c.853_856del (p.Lys285GlyfsTer?) c.782+435_782+438del (n.782+435_782+438del) c.757_760del (p.Lys253GlyfsTer?) c.397_400del (p.Lys133GlyfsTer?) c.841_844del (p.Lys281GlyfsTer?)	COSMIC COSMIC COSMIC COSMIC
17	g.7673744_7673772dup	CA2739265591	TP53	c.849_877dup (p.Gly293AlafsTer?) c.453_481dup (p.Gly161AlafsTer?) c.570_598dup (p.Gly200AlafsTer?) c.828_856dup (p.Gly286AlafsTer?) c.782+410_782+438dup (n.782+410_782+438dup) c.732_760dup (p.Gly254AlafsTer?) c.372_400dup (p.Gly134AlafsTer?) c.816_844dup (p.Gly282AlafsTer?)	ClinVar
17	g.7673744_7673806del	CA645588318	TP53	c.815_877del (p.Val272_Lys292del) c.419_481del (p.Val140_Lys160del) c.536_598del (p.Val179_Lys199del) c.794_856del (p.Val265_Lys285del) c.782+376_782+438del (n.782+376_782+438del) c.698_760del (p.Val233_Lys253del) c.338_400del (p.Val113_Lys133del) c.782_844del (p.Val261_Lys281del)	COSMIC
17	g.7673744T>A	CA397836532	TP53	c.876A>T (p.Lys292Asn) c.480A>T (p.Lys160Asn) c.597A>T (p.Lys199Asn) c.855A>T (p.Lys285Asn) c.782+437A>T (n.782+437A>T) c.759A>T (p.Lys253Asn) c.399A>T (p.Lys133Asn) c.843A>T (p.Lys281Asn)	ClinVar dbSNP COSMIC
17	g.7673744T>C	CA497715640	TP53	c.876A>G (p.Lys292=) c.480A>G (p.Lys160=) c.597A>G (p.Lys199=) c.855A>G (p.Lys285=) c.782+437A>G (n.782+437A>G) c.759A>G (p.Lys253=) c.399A>G (p.Lys133=) c.843A>G (p.Lys281=)	ClinVar dbSNP COSMIC
17	g.7673744T>G	CA397836533	TP53	c.876A>C (p.Lys292Asn) c.480A>C (p.Lys160Asn) c.597A>C (p.Lys199Asn) c.855A>C (p.Lys285Asn) c.782+437A>C (n.782+437A>C) c.759A>C (p.Lys253Asn) c.399A>C (p.Lys133Asn) c.843A>C (p.Lys281Asn)	ClinVar COSMIC
17	g.7673744T=	CA2245948805	TP53	c.876A= (p.Lys292=) c.480A= (p.Lys160=) c.597A= (p.Lys199=) c.855A= (p.Lys285=) c.782+437A= (n.782+437A=) c.759A= (p.Lys253=) c.399A= (p.Lys133=) c.843A= (p.Lys281=)
17	g.7673746dup	CA2825002639	TP53	c.876dup (p.Gly293ArgfsTer13) c.480dup (p.Gly161ArgfsTer13) c.597dup (p.Gly200ArgfsTer13) c.855dup (p.Gly286ArgfsTer13) c.782+437dup (n.782+437dup) c.759dup (p.Gly254ArgfsTer13) c.399dup (p.Gly134ArgfsTer13) c.843dup (p.Gly282ArgfsTer13)	ClinVar
17	g.7673746del	CA497715642	TP53	c.876del (p.Glu294SerfsTer?) c.480del (p.Glu162SerfsTer?) c.597del (p.Glu201SerfsTer?) c.855del (p.Glu287SerfsTer?) c.782+437del (n.782+437del) c.759del (p.Glu255SerfsTer?) c.399del (p.Glu135SerfsTer?) c.843del (p.Glu283SerfsTer?)	COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17	g.7673745_7673746del	CA645588322	TP53	c.875_876del (p.Lys292ArgfsTer13) c.479_480del (p.Lys160ArgfsTer13) c.596_597del (p.Lys199ArgfsTer13) c.854_855del (p.Lys285ArgfsTer13) c.782+436_782+437del (n.782+436_782+437del) c.758_759del (p.Lys253ArgfsTer13) c.398_399del (p.Lys133ArgfsTer13) c.842_843del (p.Lys281ArgfsTer13)	COSMIC
17	g.7673745T>A	CA000469	TP53	c.875A>T (p.Lys292Ile) c.479A>T (p.Lys160Ile) c.596A>T (p.Lys199Ile) c.854A>T (p.Lys285Ile) c.782+436A>T (n.782+436A>T) c.758A>T (p.Lys253Ile) c.398A>T (p.Lys133Ile) c.842A>T (p.Lys281Ile)	ClinVar dbSNP
17	g.7673745T>C	CA16615993	TP53	c.875A>G (p.Lys292Arg) c.479A>G (p.Lys160Arg) c.596A>G (p.Lys199Arg) c.854A>G (p.Lys285Arg) c.782+436A>G (n.782+436A>G) c.758A>G (p.Lys253Arg) c.398A>G (p.Lys133Arg) c.842A>G (p.Lys281Arg)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17	g.7673745T>G	CA397836542	TP53	c.875A>C (p.Lys292Thr) c.479A>C (p.Lys160Thr) c.596A>C (p.Lys199Thr) c.854A>C (p.Lys285Thr) c.782+436A>C (n.782+436A>C) c.758A>C (p.Lys253Thr) c.398A>C (p.Lys133Thr) c.842A>C (p.Lys281Thr)	ClinVar dbSNP COSMIC
17	g.7673745T=	CA2245948812	TP53	c.875A= (p.Lys292=) c.479A= (p.Lys160=) c.596A= (p.Lys199=) c.854A= (p.Lys285=) c.782+436A= (n.782+436A=) c.758A= (p.Lys253=) c.398A= (p.Lys133=) c.842A= (p.Lys281=)
17	g.7673746_7673768del	CA645588323	TP53	c.853_875del (p.Glu285ArgfsTer13) c.457_479del (p.Glu153ArgfsTer13) c.574_596del (p.Glu192ArgfsTer13) c.832_854del (p.Glu278ArgfsTer13) c.782+414_782+436del (n.782+414_782+436del) c.736_758del (p.Glu246ArgfsTer13) c.376_398del (p.Glu126ArgfsTer13) c.820_842del (p.Glu274ArgfsTer13)	COSMIC

Number of alleles fetched