Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7669589_7676614delCA2499224945TP53c.-19_*21del
c.-19_*310del
c.-19_*222del
c.-253_*21del
c.-136_*222del
c.-136_*21del
c.-136_*310del
c.-136_983+1021del
ClinVar
17g.7673565_7673605delCA645587356TP53c.923_963del (p.Leu308ProfsTer15)
n.923_963del (p.Leu308ProfsTer?)
n.782+576_782+616del (p.=)
c.923_963del (p.Leu308ProfsTer25)
c.923_963del (p.Leu308ProfsTer14)
c.527_567del (p.Leu176ProfsTer14)
c.527_567del (p.Leu176ProfsTer15)
c.527_567del (p.Leu176ProfsTer?)
c.527_567del (p.Leu176ProfsTer25)
c.806_846del (p.Leu269ProfsTer15)
c.806_846del (p.Leu269ProfsTer14)
c.446_486del (p.Leu149ProfsTer14)
n.890_930del (p.Leu297ProfsTer15)
c.446_486del (p.Leu149ProfsTer25)
c.446_486del (p.Leu149ProfsTer15)
c.806_846del (p.Leu269ProfsTer25)
COSMIC
17g.7673592_7673610delCA645587376TP53c.921_939del
n.921_939del
n.782+574_782+592del (p.=)
c.525_543del
c.804_822del
c.444_462del
n.888_906del
COSMIC
17g.7673592_7673702delCA645587377TP53c.919+1_938del
n.919+1_938del
n.782+481_782+591del (p.=)
c.523+1_542del
c.802+1_821del
c.442+1_461del
n.886+1_905del
COSMIC
17g.7673598_7673702delCA645587380TP53c.919_931del
n.919_931del
n.782+480_782+584del (p.=)
c.523_535del
c.802_814del
c.442_454del
n.886_898del
COSMIC
17g.7673598_7673600delinsCAACA645587381TP53c.928_930delinsTTG (p.Asn310Leu)
n.928_930delinsTTG (p.Asn310Leu)
n.782+581_782+583delinsTTG (p.=)
c.532_534delinsTTG (p.Asn178Leu)
c.811_813delinsTTG (p.Asn271Leu)
c.451_453delinsTTG (p.Asn151Leu)
n.895_897delinsTTG (p.Asn299Leu)
COSMIC
17g.7673600dupCA497714339TP53c.929dup (p.Asn310LysfsTer27)
n.929dup (p.Asn310LysfsTer?)
n.782+582dup (p.=)
c.929dup (p.Asn310LysfsTer?)
c.929dup (p.Asn310LysfsTer26)
c.533dup (p.Asn178LysfsTer26)
c.533dup (p.Asn178LysfsTer27)
c.533dup (p.Asn178LysfsTer?)
c.812dup (p.Asn271LysfsTer27)
c.812dup (p.Asn271LysfsTer26)
c.452dup (p.Asn151LysfsTer26)
n.896dup (p.Asn299LysfsTer27)
c.452dup (p.Asn151LysfsTer?)
c.452dup (p.Asn151LysfsTer27)
c.812dup (p.Asn271LysfsTer?)
17g.7673600T>ACA397836121TP53c.928A>T (p.Asn310Tyr)
n.928A>T (p.Asn310Tyr)
n.782+581A>T (p.=)
c.532A>T (p.Asn178Tyr)
c.811A>T (p.Asn271Tyr)
c.451A>T (p.Asn151Tyr)
n.895A>T (p.Asn299Tyr)
17g.7673600T>CCA397836124TP53c.928A>G (p.Asn310Asp)
n.928A>G (p.Asn310Asp)
n.782+581A>G (p.=)
c.532A>G (p.Asn178Asp)
c.811A>G (p.Asn271Asp)
c.451A>G (p.Asn151Asp)
n.895A>G (p.Asn299Asp)
ClinVar COSMIC
17g.7673600T>GCA397836126TP53c.928A>C (p.Asn310His)
n.928A>C (p.Asn310His)
n.782+581A>C (p.=)
c.532A>C (p.Asn178His)
c.811A>C (p.Asn271His)
c.451A>C (p.Asn151His)
n.895A>C (p.Asn299His)
COSMIC COSMIC COSMIC COSMIC
17g.7673600T=CA2245947978TP53c.928A= (p.Asn310=)
n.928A= (p.Asn310=)
n.782+581A= (p.=)
c.532A= (p.Asn178=)
c.811A= (p.Asn271=)
c.451A= (p.Asn151=)
n.895A= (p.Asn299=)
17g.7673600_7673601delinsTGCA2245947981TP53c.927_928delinsCA (p.Pro309=)
n.927_928delinsCA (p.Pro309=)
n.782+580_782+581delinsCA (p.=)
c.531_532delinsCA (p.Pro177=)
c.810_811delinsCA (p.Pro270=)
c.450_451delinsCA (p.Pro150=)
n.894_895delinsCA (p.Pro298=)
17g.7673600_7673604delCA645587385TP53c.924_928del (p.Pro309GlnfsTer26)
n.924_928del (p.Pro309GlnfsTer?)
n.782+577_782+581del (p.=)
c.924_928del (p.Pro309GlnfsTer?)
c.924_928del (p.Pro309GlnfsTer25)
c.528_532del (p.Pro177GlnfsTer25)
c.528_532del (p.Pro177GlnfsTer26)
c.528_532del (p.Pro177GlnfsTer?)
c.807_811del (p.Pro270GlnfsTer26)
c.807_811del (p.Pro270GlnfsTer25)
c.447_451del (p.Pro150GlnfsTer25)
n.891_895del (p.Pro298GlnfsTer26)
c.447_451del (p.Pro150GlnfsTer?)
c.447_451del (p.Pro150GlnfsTer26)
c.807_811del (p.Pro270GlnfsTer?)
COSMIC
17g.7673600_7673614delCA645587386TP53c.920-6_928del
n.920-6_928del
n.782+567_782+581del (p.=)
c.524-6_532del
c.803-6_811del
c.443-6_451del
n.887-6_895del
COSMIC
17g.7673601G>ACA497714349TP53c.927C>T (p.Pro309=)
n.927C>T (p.Pro309=)
n.782+580C>T (p.=)
c.531C>T (p.Pro177=)
c.810C>T (p.Pro270=)
c.450C>T (p.Pro150=)
n.894C>T (p.Pro298=)
gnomAD
17g.7673601G>CCA497714350TP53c.927C>G (p.Pro309=)
n.927C>G (p.Pro309=)
n.782+580C>G (p.=)
c.531C>G (p.Pro177=)
c.810C>G (p.Pro270=)
c.450C>G (p.Pro150=)
n.894C>G (p.Pro298=)
17g.7673601G=CA2245947993TP53c.927C= (p.Pro309=)
n.927C= (p.Pro309=)
n.782+580C= (p.=)
c.531C= (p.Pro177=)
c.810C= (p.Pro270=)
c.450C= (p.Pro150=)
n.894C= (p.Pro298=)
17g.7673601G>TCA497714352TP53c.927C>A (p.Pro309=)
n.927C>A (p.Pro309=)
n.782+580C>A (p.=)
c.531C>A (p.Pro177=)
c.810C>A (p.Pro270=)
c.450C>A (p.Pro150=)
n.894C>A (p.Pro298=)
ClinVar COSMIC
17g.7673603delCA497714355TP53c.927del (p.Asn310ThrfsTer?)
n.927del (p.Asn310ThrfsTer?)
n.782+580del (p.=)
c.531del (p.Asn178ThrfsTer?)
c.810del (p.Asn271ThrfsTer?)
c.450del (p.Asn151ThrfsTer?)
n.894del (p.Asn299ThrfsTer?)
ClinVar dbSNP COSMIC COSMIC
17g.7673602G>ACA397836130TP53c.926C>T (p.Pro309Leu)
n.926C>T (p.Pro309Leu)
n.782+579C>T (p.=)
c.530C>T (p.Pro177Leu)
c.809C>T (p.Pro270Leu)
c.449C>T (p.Pro150Leu)
n.893C>T (p.Pro298Leu)
17g.7673602G>CCA397836137TP53c.926C>G (p.Pro309Arg)
n.926C>G (p.Pro309Arg)
n.782+579C>G (p.=)
c.530C>G (p.Pro177Arg)
c.809C>G (p.Pro270Arg)
c.449C>G (p.Pro150Arg)
n.893C>G (p.Pro298Arg)
COSMIC
17g.7673602G>TCA397836134TP53c.926C>A (p.Pro309His)
n.926C>A (p.Pro309His)
n.782+579C>A (p.=)
c.530C>A (p.Pro177His)
c.809C>A (p.Pro270His)
c.449C>A (p.Pro150His)
n.893C>A (p.Pro298His)
17g.7673606_7673622delCA645587387TP53c.920-10_926del
n.920-10_926del
n.782+563_782+579del (p.=)
c.524-10_530del
c.803-10_809del
c.443-10_449del
n.887-10_893del
COSMIC COSMIC COSMIC COSMIC
17g.7673603G>ACA397836140TP53c.925C>T (p.Pro309Ser)
n.925C>T (p.Pro309Ser)
n.782+578C>T (p.=)
c.529C>T (p.Pro177Ser)
c.808C>T (p.Pro270Ser)
c.448C>T (p.Pro150Ser)
n.892C>T (p.Pro298Ser)
ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673603G>CCA397836142TP53c.925C>G (p.Pro309Ala)
n.925C>G (p.Pro309Ala)
n.782+578C>G (p.=)
c.529C>G (p.Pro177Ala)
c.808C>G (p.Pro270Ala)
c.448C>G (p.Pro150Ala)
n.892C>G (p.Pro298Ala)
17g.7673603G=CA2245948005TP53c.925C= (p.Pro309=)
n.925C= (p.Pro309=)
n.782+578C= (p.=)
c.529C= (p.Pro177=)
c.808C= (p.Pro270=)
c.448C= (p.Pro150=)
n.892C= (p.Pro298=)
17g.7673603G>TCA397836145TP53c.925C>A (p.Pro309Thr)
n.925C>A (p.Pro309Thr)
n.782+578C>A (p.=)
c.529C>A (p.Pro177Thr)
c.808C>A (p.Pro270Thr)
c.448C>A (p.Pro150Thr)
n.892C>A (p.Pro298Thr)
17g.7673604C>ACA497714384TP53c.924G>T (p.Leu308=)
n.924G>T (p.Leu308=)
n.782+577G>T (p.=)
c.528G>T (p.Leu176=)
c.807G>T (p.Leu269=)
c.447G>T (p.Leu149=)
n.891G>T (p.Leu297=)
17g.7673604C=CA2245948012TP53c.924G= (p.Leu308=)
n.924G= (p.Leu308=)
n.782+577G= (p.=)
c.528G= (p.Leu176=)
c.807G= (p.Leu269=)
c.447G= (p.Leu149=)
n.891G= (p.Leu297=)
17g.7673604C>GCA16615992TP53c.924G>C (p.Leu308=)
n.924G>C (p.Leu308=)
n.782+577G>C (p.=)
c.528G>C (p.Leu176=)
c.807G>C (p.Leu269=)
c.447G>C (p.Leu149=)
n.891G>C (p.Leu297=)
ClinVar COSMIC
17g.7673604C>TCA000503TP53c.924G>A (p.Leu308=)
n.924G>A (p.Leu308=)
n.782+577G>A (p.=)
c.528G>A (p.Leu176=)
c.807G>A (p.Leu269=)
c.447G>A (p.Leu149=)
n.891G>A (p.Leu297=)
ClinVar dbSNP gnomAD COSMIC
17g.7673610_7673611insCAACAGTGCTCA645587389TP53c.924_925insTTGAGCACTG
n.924_925insTTGAGCACTG
n.782+577_782+578insTTGAGCACTG (p.=)
c.528_529insTTGAGCACTG
c.807_808insTTGAGCACTG
c.447_448insTTGAGCACTG
n.891_892insTTGAGCACTG
COSMIC COSMIC COSMIC COSMIC
17g.7673605A>CCA397836151TP53c.923T>G (p.Leu308Arg)
n.923T>G (p.Leu308Arg)
n.782+576T>G (p.=)
c.527T>G (p.Leu176Arg)
c.806T>G (p.Leu269Arg)
c.446T>G (p.Leu149Arg)
n.890T>G (p.Leu297Arg)
17g.7673605A>GCA397836154TP53c.923T>C (p.Leu308Pro)
n.923T>C (p.Leu308Pro)
n.782+576T>C (p.=)
c.527T>C (p.Leu176Pro)
c.806T>C (p.Leu269Pro)
c.446T>C (p.Leu149Pro)
n.890T>C (p.Leu297Pro)
17g.7673605A>TCA397836155TP53c.923T>A (p.Leu308Gln)
n.923T>A (p.Leu308Gln)
n.782+576T>A (p.=)
c.527T>A (p.Leu176Gln)
c.806T>A (p.Leu269Gln)
c.446T>A (p.Leu149Gln)
n.890T>A (p.Leu297Gln)
17g.7673606G>ACA497714399TP53c.922C>T (p.Leu308=)
n.922C>T (p.Leu308=)
n.782+575C>T (p.=)
c.526C>T (p.Leu176=)
c.805C>T (p.Leu269=)
c.445C>T (p.Leu149=)
n.889C>T (p.Leu297=)
ClinVar
17g.7673606G>CCA397836159TP53c.922C>G (p.Leu308Val)
n.922C>G (p.Leu308Val)
n.782+575C>G (p.=)
c.526C>G (p.Leu176Val)
c.805C>G (p.Leu269Val)
c.445C>G (p.Leu149Val)
n.889C>G (p.Leu297Val)
COSMIC COSMIC COSMIC COSMIC
17g.7673606G=CA2245948029TP53c.922C= (p.Leu308=)
n.922C= (p.Leu308=)
n.782+575C= (p.=)
c.526C= (p.Leu176=)
c.805C= (p.Leu269=)
c.445C= (p.Leu149=)
n.889C= (p.Leu297=)
17g.7673606G>TCA397836161TP53c.922C>A (p.Leu308Met)
n.922C>A (p.Leu308Met)
n.782+575C>A (p.=)
c.526C>A (p.Leu176Met)
c.805C>A (p.Leu269Met)
c.445C>A (p.Leu149Met)
n.889C>A (p.Leu297Met)
COSMIC
17g.7673607_7673608delCA645587390TP53c.921_922del (p.Leu308AlafsTer28)
n.921_922del (p.Leu308AlafsTer?)
n.782+574_782+575del (p.=)
c.921_922del (p.Leu308AlafsTer?)
c.921_922del (p.Leu308AlafsTer27)
c.525_526del (p.Leu176AlafsTer27)
c.525_526del (p.Leu176AlafsTer28)
c.525_526del (p.Leu176AlafsTer?)
c.804_805del (p.Leu269AlafsTer28)
c.804_805del (p.Leu269AlafsTer27)
c.444_445del (p.Leu149AlafsTer27)
n.888_889del (p.Leu297AlafsTer28)
c.444_445del (p.Leu149AlafsTer?)
c.444_445del (p.Leu149AlafsTer28)
c.804_805del (p.Leu269AlafsTer?)
COSMIC COSMIC COSMIC COSMIC
17g.7673607T>ACA497714414TP53c.921A>T (p.Ala307=)
n.921A>T (p.Ala307=)
n.782+574A>T (p.=)
c.525A>T (p.Ala175=)
c.804A>T (p.Ala268=)
c.444A>T (p.Ala148=)
n.888A>T (p.Ala296=)
17g.7673607T>CCA497714418TP53c.921A>G (p.Ala307=)
n.921A>G (p.Ala307=)
n.782+574A>G (p.=)
c.525A>G (p.Ala175=)
c.804A>G (p.Ala268=)
c.444A>G (p.Ala148=)
n.888A>G (p.Ala296=)
COSMIC
17g.7673607T>GCA497714421TP53c.921A>C (p.Ala307=)
n.921A>C (p.Ala307=)
n.782+574A>C (p.=)
c.525A>C (p.Ala175=)
c.804A>C (p.Ala268=)
c.444A>C (p.Ala148=)
n.888A>C (p.Ala296=)
17g.7673607T=CA2245948035TP53c.921A= (p.Ala307=)
n.921A= (p.Ala307=)
n.782+574A= (p.=)
c.525A= (p.Ala175=)
c.804A= (p.Ala268=)
c.444A= (p.Ala148=)
n.888A= (p.Ala296=)
17g.7673608G>ACA397836165TP53c.920C>T (p.Ala307Val)
n.920C>T (p.Ala307Val)
n.782+573C>T (p.=)
c.524C>T (p.Ala175Val)
c.803C>T (p.Ala268Val)
c.443C>T (p.Ala148Val)
n.887C>T (p.Ala296Val)
ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673608G>CCA397836168TP53c.920C>G (p.Ala307Gly)
n.920C>G (p.Ala307Gly)
n.782+573C>G (p.=)
c.524C>G (p.Ala175Gly)
c.803C>G (p.Ala268Gly)
c.443C>G (p.Ala148Gly)
n.887C>G (p.Ala296Gly)
ClinVar
17g.7673608G=CA2245948041TP53c.920C= (p.Ala307=)
n.920C= (p.Ala307=)
n.782+573C= (p.=)
c.524C= (p.Ala175=)
c.803C= (p.Ala268=)
c.443C= (p.Ala148=)
n.887C= (p.Ala296=)
17g.7673608G>TCA397836170TP53c.920C>A (p.Ala307Glu)
n.920C>A (p.Ala307Glu)
n.782+573C>A (p.=)
c.524C>A (p.Ala175Glu)
c.803C>A (p.Ala268Glu)
c.443C>A (p.Ala148Glu)
n.887C>A (p.Ala296Glu)
17g.7673609C>ACA397836174TP53c.920-1G>T (p.=)
n.920-1G>T (p.=)
n.782+572G>T (p.=)
c.524-1G>T (p.=)
c.803-1G>T (p.=)
c.443-1G>T (p.=)
n.887-1G>T (p.=)
ClinVar COSMIC COSMIC COSMIC COSMIC
17g.7673609C=CA2245948059TP53c.920-1G= (p.=)
n.920-1G= (p.=)
n.782+572G= (p.=)
c.524-1G= (p.=)
c.803-1G= (p.=)
c.443-1G= (p.=)
n.887-1G= (p.=)

Number of alleles fetched