Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1401365_1401373delCA2582641917GAMTc.107_115del (p.Ile36_Gly38del)
c.107_112+3del
gnomAD v4
19g.1401370A>CCA402998148GAMTc.107T>G (p.Ile36Ser)
19g.1401370A>GCA402998149GAMTc.107T>C (p.Ile36Thr)
gnomAD v4
19g.1401370A>TCA402998150GAMTc.107T>A (p.Ile36Asn)
gnomAD v4
19g.1401371T>ACA402998152GAMTc.106A>T (p.Ile36Phe)
19g.1401371T>CCA402998154GAMTc.106A>G (p.Ile36Val)
ClinVar dbSNP gnomAD v4
19g.1401371T>GCA402998156GAMTc.106A>C (p.Ile36Leu)
19g.1401371T=CA2317700418GAMTc.106A= (p.Ile36=)
19g.1401372G>ACA9043802GAMTc.105C>T (p.Arg35=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401372G>CCA504731645GAMTc.105C>G (p.Arg35=)
gnomAD v4
19g.1401372G=CA2317700419GAMTc.105C= (p.Arg35=)
19g.1401372G>TCA504731646GAMTc.105C>A (p.Arg35=)
gnomAD v4
19g.1401373C>ACA402998160GAMTc.104G>T (p.Arg35Leu)
gnomAD v4
19g.1401373C>GCA402998161GAMTc.104G>C (p.Arg35Pro)
19g.1401373C>TCA402998163GAMTc.104G>A (p.Arg35His)
gnomAD v4
19g.1401374G>ACA402998168GAMTc.103C>T (p.Arg35Cys)
gnomAD v4
19g.1401374G>CCA402998167GAMTc.103C>G (p.Arg35Gly)
19g.1401374G>TCA402998165GAMTc.103C>A (p.Arg35Ser)
gnomAD v4
19g.1401375C>ACA9043803GAMTc.102G>T (p.Leu34=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401375C=CA2317700420GAMTc.102G= (p.Leu34=)
19g.1401375C>GCA504731647GAMTc.102G>C (p.Leu34=)
19g.1401375C>TCA504731648GAMTc.102G>A (p.Leu34=)
gnomAD v4
19g.1401376A=CA2317700421GAMTc.101T= (p.Leu34=)
19g.1401376A>CCA402998169GAMTc.101T>G (p.Leu34Arg)
19g.1401376A>GCA402998170GAMTc.101T>C (p.Leu34Pro)
dbSNP gnomAD v3 gnomAD v4
19g.1401376A>TCA402998172GAMTc.101T>A (p.Leu34Gln)
gnomAD v4
19g.1401377G>ACA504731649GAMTc.100C>T (p.Leu34=)
ClinVar dbSNP gnomAD v4
19g.1401377G>CCA402998174GAMTc.100C>G (p.Leu34Val)
gnomAD v4
19g.1401377G>TCA402998176GAMTc.100C>A (p.Leu34Met)
gnomAD v4
19g.1401378G>ACA504731650GAMTc.99C>T (p.His33=)
gnomAD v4
19g.1401378G>CCA402998178GAMTc.99C>G (p.His33Gln)
19g.1401378G>TCA402998177GAMTc.99C>A (p.His33Gln)
gnomAD v4
19g.1401379T>ACA402998181GAMTc.98A>T (p.His33Leu)
19g.1401379T>CCA402998182GAMTc.98A>G (p.His33Arg)
gnomAD v4
19g.1401379T>GCA402998183GAMTc.98A>C (p.His33Pro)
gnomAD v4
19g.1401380G>ACA402998185GAMTc.97C>T (p.His33Tyr)
dbSNP gnomAD v4
19g.1401380G>CCA402998187GAMTc.97C>G (p.His33Asp)
19g.1401380G=CA2317700422GAMTc.97C= (p.His33=)
19g.1401380G>TCA402998188GAMTc.97C>A (p.His33Asn)
gnomAD v4
19g.1401381C>ACA504731651GAMTc.96G>T (p.Thr32=)
gnomAD v4
19g.1401381C=CA2317700423GAMTc.96G= (p.Thr32=)
19g.1401381C>GCA504731653GAMTc.96G>C (p.Thr32=)
19g.1401381C>TCA504731652GAMTc.96G>A (p.Thr32=)
ClinVar dbSNP gnomAD v4
19g.1401382G>ACA402998190GAMTc.95C>T (p.Thr32Met)
gnomAD v4
19g.1401382G>CCA402998192GAMTc.95C>G (p.Thr32Arg)
gnomAD v4
19g.1401382G>TCA402998191GAMTc.95C>A (p.Thr32Lys)
gnomAD v4
19g.1401384_1401385delCA2582641919GAMTc.94_95del (p.Thr32AlafsTer?)
c.94_95del (p.Thr32AlafsTer29)
gnomAD v4
19g.1401383T>ACA402998193GAMTc.94A>T (p.Thr32Ser)
gnomAD v4
19g.1401383T>CCA402998195GAMTc.94A>G (p.Thr32Ala)
gnomAD v4
19g.1401383T>GCA402998196GAMTc.94A>C (p.Thr32Pro)
19g.1401384G>ACA504731654GAMTc.93C>T (p.Asp31=)
dbSNP gnomAD v3 gnomAD v4
19g.1401384G>CCA402998198GAMTc.93C>G (p.Asp31Glu)
19g.1401384G=CA2317700424GAMTc.93C= (p.Asp31=)
19g.1401384G>TCA402998200GAMTc.93C>A (p.Asp31Glu)
gnomAD v4
19g.1401385T>ACA314844GAMTc.92A>T (p.Asp31Val)
ClinVar dbSNP gnomAD v4
19g.1401385T>CCA402998201GAMTc.92A>G (p.Asp31Gly)
gnomAD v4
19g.1401385T>GCA402998202GAMTc.92A>C (p.Asp31Ala)
19g.1401385T=CA2317700425GAMTc.92A= (p.Asp31=)
19g.1401386C>ACA402998204GAMTc.91G>T (p.Asp31Tyr)
gnomAD v4
19g.1401386C>GCA402998206GAMTc.91G>C (p.Asp31His)
19g.1401386C>TCA402998210GAMTc.91G>A (p.Asp31Asn)
gnomAD v4
19g.1401388_1401389insTGCCGCA631301069GAMTc.91_92insCACGG (p.Asp31AlafsTer13)
c.91_92insCACGG (p.Asp31AlafsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401387C>ACA504731655GAMTc.90G>T (p.Ala30=)
gnomAD v4
19g.1401387C>GCA504731656GAMTc.90G>C (p.Ala30=)
gnomAD v4
19g.1401387C>TCA504731657GAMTc.90G>A (p.Ala30=)
ClinVar dbSNP gnomAD v4
19g.1401388_1401389delCA2582641920GAMTc.89_90del (p.Ala30GlyfsTer?)
gnomAD v4
19g.1401388G>ACA402998216GAMTc.89C>T (p.Ala30Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401388G>CCA402998215GAMTc.89C>G (p.Ala30Gly)
dbSNP gnomAD v3 gnomAD v4
19g.1401388G=CA2317700426GAMTc.89C= (p.Ala30=)
19g.1401388G>TCA402998213GAMTc.89C>A (p.Ala30Glu)
gnomAD v4
19g.1401389C>ACA402998220GAMTc.88G>T (p.Ala30Ser)
gnomAD v4
19g.1401389C=CA2317700427GAMTc.88G= (p.Ala30=)
19g.1401389C>GCA402998218GAMTc.88G>C (p.Ala30Pro)
dbSNP gnomAD v2 gnomAD v4
19g.1401389C>TCA402998221GAMTc.88G>A (p.Ala30Thr)
gnomAD v4
19g.1401390T>ACA504731660GAMTc.87A>T (p.Ala29=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401390T>CCA504731661GAMTc.87A>G (p.Ala29=)
gnomAD v4
19g.1401390T>GCA504731659GAMTc.87A>C (p.Ala29=)
dbSNP gnomAD v2 gnomAD v4
19g.1401390T=CA2317700428GAMTc.87A= (p.Ala29=)
19g.1401391G>ACA402998223GAMTc.86C>T (p.Ala29Val)
gnomAD v4
19g.1401391G>CCA402998224GAMTc.86C>G (p.Ala29Gly)
19g.1401391G>TCA402998226GAMTc.86C>A (p.Ala29Glu)
gnomAD v4
19g.1401392C>ACA402998228GAMTc.85G>T (p.Ala29Ser)
gnomAD v4
19g.1401392C=CA2317700429GAMTc.85G= (p.Ala29=)
19g.1401392C>GCA402998230GAMTc.85G>C (p.Ala29Pro)
19g.1401392C>TCA402998231GAMTc.85G>A (p.Ala29Thr)
ClinVar dbSNP gnomAD v4
19g.1401393G>ACA9043804GAMTc.84C>T (p.Asp28=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401393G>CCA402998234GAMTc.84C>G (p.Asp28Glu)
19g.1401393G=CA2317700430GAMTc.84C= (p.Asp28=)
19g.1401393G>TCA402998236GAMTc.84C>A (p.Asp28Glu)
gnomAD v4
19g.1401394T>ACA402998237GAMTc.83A>T (p.Asp28Val)
19g.1401394T>CCA402998239GAMTc.83A>G (p.Asp28Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401394T>GCA402998240GAMTc.83A>C (p.Asp28Ala)
dbSNP gnomAD v3 gnomAD v4
19g.1401394T=CA2317700431GAMTc.83A= (p.Asp28=)
19g.1401395C>ACA402998246GAMTc.82G>T (p.Asp28Tyr)
gnomAD v4
19g.1401395C=CA2317700432GAMTc.82G= (p.Asp28=)
19g.1401395C>GCA402998242GAMTc.82G>C (p.Asp28His)
dbSNP gnomAD v2 gnomAD v4
19g.1401395C>TCA402998244GAMTc.82G>A (p.Asp28Asn)
gnomAD v4
19g.1401395dupCA2580096099GAMTc.82dup (p.Asp28GlyfsTer?)
ClinVar
19g.1401396G>ACA504731663GAMTc.81C>T (p.Tyr27=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.1401396G>CCA304067316GAMTc.81C>G (p.Tyr27Ter)
dbSNP gnomAD v3 gnomAD v4
19g.1401396G=CA2317700433GAMTc.81C= (p.Tyr27=)
19g.1401396G>TCA402998248GAMTc.81C>A (p.Tyr27Ter)
gnomAD v4
19g.1401396dupCA2582641921GAMTc.81dup (p.Asp28ArgfsTer?)
gnomAD v4
19g.1401397T>ACA9043805GAMTc.80A>T (p.Tyr27Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401397T>CCA402998251GAMTc.80A>G (p.Tyr27Cys)
gnomAD v4
19g.1401397T>GCA402998253GAMTc.80A>C (p.Tyr27Ser)
19g.1401397T=CA2317700434GAMTc.80A= (p.Tyr27=)
19g.1401398A=CA2317700435GAMTc.79T= (p.Tyr27=)
19g.1401398A>CCA402998254GAMTc.79T>G (p.Tyr27Asp)
19g.1401398A>GCA295620GAMTc.79T>C (p.Tyr27His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401398A>TCA402998256GAMTc.79T>A (p.Tyr27Asn)
19g.1401399G>ACA504731665GAMTc.78C>T (p.Ala26=)
gnomAD v4
19g.1401399G>CCA504731666GAMTc.78C>G (p.Ala26=)
19g.1401399G>TCA504731667GAMTc.78C>A (p.Ala26=)
gnomAD v4
19g.1401400G>ACA402998258GAMTc.77C>T (p.Ala26Val)
gnomAD v4
19g.1401400G>CCA402998260GAMTc.77C>G (p.Ala26Gly)
gnomAD v4
19g.1401400G>TCA402998262GAMTc.77C>A (p.Ala26Asp)
gnomAD v4
19g.1401401C>ACA402998265GAMTc.76G>T (p.Ala26Ser)
dbSNP gnomAD v4
19g.1401401C=CA2317700436GAMTc.76G= (p.Ala26=)
19g.1401401C>GCA402998266GAMTc.76G>C (p.Ala26Pro)
19g.1401401C>TCA402998263GAMTc.76G>A (p.Ala26Thr)
gnomAD v4
19g.1401402C>ACA504731672GAMTc.75G>T (p.Ala25=)
gnomAD v4
19g.1401402C=CA2317700437GAMTc.75G= (p.Ala25=)
19g.1401402C>GCA504731673GAMTc.75G>C (p.Ala25=)
19g.1401402C>TCA9043806GAMTc.75G>A (p.Ala25=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401403G>ACA402998268GAMTc.74C>T (p.Ala25Val)
gnomAD v4
19g.1401403G>CCA402998270GAMTc.74C>G (p.Ala25Gly)
19g.1401403G=CA2317700438GAMTc.74C= (p.Ala25=)
19g.1401403G>TCA402998271GAMTc.74C>A (p.Ala25Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401404delCA2582641922GAMTc.73del (p.Ala25ArgfsTer17)
c.73del (p.Ala25ArgfsTer?)
gnomAD v4
19g.1401404C>ACA9043807GAMTc.73G>T (p.Ala25Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401404C=CA2317700439GAMTc.73G= (p.Ala25=)
19g.1401404C>GCA402998274GAMTc.73G>C (p.Ala25Pro)
19g.1401404C>TCA402998276GAMTc.73G>A (p.Ala25Thr)
gnomAD v4
19g.1401406_1401509delCA2582641923GAMTc.-31_73del
gnomAD v4
19g.1401405G>ACA504731674GAMTc.72C>T (p.Pro24=)
gnomAD v4
19g.1401405G>CCA504731678GAMTc.72C>G (p.Pro24=)
19g.1401405G>TCA504731679GAMTc.72C>A (p.Pro24=)
ClinVar gnomAD v4
19g.1401407dupCA2813256122GAMTc.72dup (p.Ala25ArgfsTer?)
19g.1401407delCA2582641924GAMTc.72del (p.Ala25ArgfsTer17)
c.72del (p.Ala25ArgfsTer?)
gnomAD v4
19g.1401406G>ACA402998278GAMTc.71C>T (p.Pro24Leu)
gnomAD v4
19g.1401406G>CCA402998280GAMTc.71C>G (p.Pro24Arg)
gnomAD v4
19g.1401406G>TCA402998282GAMTc.71C>A (p.Pro24His)
gnomAD v4
19g.1401407G>ACA402998284GAMTc.70C>T (p.Pro24Ser)
gnomAD v4
19g.1401407G>CCA402998285GAMTc.70C>G (p.Pro24Ala)
19g.1401407G>TCA402998287GAMTc.70C>A (p.Pro24Thr)
gnomAD v4
19g.1401408C>ACA504731680GAMTc.69G>T (p.Ala23=)
gnomAD v4
19g.1401408C>GCA504731681GAMTc.69G>C (p.Ala23=)
ClinVar
19g.1401408C>TCA504731682GAMTc.69G>A (p.Ala23=)
gnomAD v4
19g.1401409G>ACA314842GAMTc.68C>T (p.Ala23Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401409G>CCA402998290GAMTc.68C>G (p.Ala23Gly)
dbSNP gnomAD v4
19g.1401409G=CA2317700440GAMTc.68C= (p.Ala23=)
19g.1401409G>TCA402998289GAMTc.68C>A (p.Ala23Glu)
gnomAD v4
19g.1401410C>ACA402998293GAMTc.67G>T (p.Ala23Ser)
gnomAD v4
19g.1401410C=CA2317700441GAMTc.67G= (p.Ala23=)
19g.1401410C>GCA402998295GAMTc.67G>C (p.Ala23Pro)
19g.1401410C>TCA9043808GAMTc.67G>A (p.Ala23Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401411C>ACA504731684GAMTc.66G>T (p.Ala22=)
ClinVar gnomAD v4
19g.1401411C=CA2317700442GAMTc.66G= (p.Ala22=)
19g.1401411C>GCA504731685GAMTc.66G>C (p.Ala22=)
19g.1401411C>TCA9043809GAMTc.66G>A (p.Ala22=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401412_1401413delCA2582641925GAMTc.65_66del (p.Ala22GlyfsTer?)
gnomAD v4
19g.1401412delCA2580096101GAMTc.65del (p.Ala22GlyfsTer20)
c.65del (p.Ala22GlyfsTer?)
ClinVar gnomAD v4
19g.1401412G>ACA402998296GAMTc.65C>T (p.Ala22Val)
gnomAD v4
19g.1401412G>CCA402998298GAMTc.65C>G (p.Ala22Gly)
gnomAD v4
19g.1401412G>TCA402998300GAMTc.65C>A (p.Ala22Glu)
gnomAD v4
19g.1401412_1401413delinsGCCA2317700443GAMTc.64_65delinsGC (p.Ala22=)
19g.1401413C>ACA402998301GAMTc.64G>T (p.Ala22Ser)
gnomAD v4
19g.1401413C=CA2317700444GAMTc.64G= (p.Ala22=)
19g.1401413C>GCA402998303GAMTc.64G>C (p.Ala22Pro)
19g.1401413C>TCA10651555GAMTc.64G>A (p.Ala22Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401418dupCA631301051GAMTc.64dup (p.Ala22GlyfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.1401417_1401418dupCA2582641926GAMTc.63_64dup (p.Ala22GlyfsTer21)
c.63_64dup (p.Ala22GlyfsTer?)
gnomAD v4
19g.1401418delCA631301050GAMTc.64del (p.Ala22ArgfsTer20)
c.64del (p.Ala22ArgfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.1401414C>ACA504731691GAMTc.63G>T (p.Gly21=)
gnomAD v4
19g.1401414C>GCA504731692GAMTc.63G>C (p.Gly21=)
gnomAD v4
19g.1401414C>TCA504731693GAMTc.63G>A (p.Gly21=)
gnomAD v4
19g.1401415C>ACA402998306GAMTc.62G>T (p.Gly21Val)
gnomAD v4
19g.1401415C>GCA402998308GAMTc.62G>C (p.Gly21Ala)
19g.1401415C>TCA402998310GAMTc.62G>A (p.Gly21Glu)
ClinVar gnomAD v4
19g.1401416C>ACA402998314GAMTc.61G>T (p.Gly21Trp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401416C=CA2317700445GAMTc.61G= (p.Gly21=)
19g.1401416C>GCA402998316GAMTc.61G>C (p.Gly21Arg)
gnomAD v4
19g.1401416C>TCA402998313GAMTc.61G>A (p.Gly21Arg)
gnomAD v4
19g.1401417C>ACA402998320GAMTc.60G>T (p.Trp20Cys)
gnomAD v4
19g.1401417C=CA2317700446GAMTc.60G= (p.Trp20=)
19g.1401417C>GCA402998323GAMTc.60G>C (p.Trp20Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401417C>TCA402998322GAMTc.60G>A (p.Trp20Ter)
ClinVar gnomAD v4
19g.1401418C>ACA402998326GAMTc.59G>T (p.Trp20Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401418C=CA2317700447GAMTc.59G= (p.Trp20=)
19g.1401418C>GCA340769GAMTc.59G>C (p.Trp20Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401418C>TCA402998328GAMTc.59G>A (p.Trp20Ter)
ClinVar dbSNP gnomAD v4
19g.1401419A>CCA402998332GAMTc.58T>G (p.Trp20Gly)
19g.1401419A>GCA402998334GAMTc.58T>C (p.Trp20Arg)
gnomAD v4
19g.1401419A>TCA402998333GAMTc.58T>A (p.Trp20Arg)
19g.1401419dupCA504731701GAMTc.58dup (p.Trp20LeufsTer?)
ClinVar gnomAD v4
19g.1401420C>ACA504731707GAMTc.57G>T (p.Ala19=)
gnomAD v4
19g.1401420C=CA2317700448GAMTc.57G= (p.Ala19=)
19g.1401420C>GCA504731706GAMTc.57G>C (p.Ala19=)
dbSNP gnomAD v3 gnomAD v4
19g.1401420C>TCA504731704GAMTc.57G>A (p.Ala19=)
gnomAD v4
19g.1401421G>ACA402998335GAMTc.56C>T (p.Ala19Val)
gnomAD v4
19g.1401421G>CCA402998336GAMTc.56C>G (p.Ala19Gly)
19g.1401421G>TCA402998337GAMTc.56C>A (p.Ala19Glu)
gnomAD v4
19g.1401422C>ACA402998341GAMTc.55G>T (p.Ala19Ser)
gnomAD v4
19g.1401422C=CA2317700449GAMTc.55G= (p.Ala19=)
19g.1401422C>GCA402998343GAMTc.55G>C (p.Ala19Pro)
dbSNP gnomAD v4
19g.1401422C>TCA402998344GAMTc.55G>A (p.Ala19Thr)
gnomAD v4
19g.1401422_1401423insACA2813256133GAMTc.54_55insT (p.Ala19CysfsTer?)
19g.1401423G>ACA304067345GAMTc.54C>T (p.Pro18=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401423G>CCA504731709GAMTc.54C>G (p.Pro18=)
ClinVar gnomAD v4
19g.1401423G=CA2317700450GAMTc.54C= (p.Pro18=)
19g.1401423G>TCA504731711GAMTc.54C>A (p.Pro18=)
gnomAD v4
19g.1401426dupCA2813256134GAMTc.54dup (p.Ala19ArgfsTer?)
19g.1401426delCA2582641927GAMTc.54del (p.Ala19ArgfsTer23)
c.54del (p.Ala19ArgfsTer?)
gnomAD v4
19g.1401424G>ACA402998345GAMTc.53C>T (p.Pro18Leu)
ClinVar dbSNP gnomAD v4
19g.1401424G>CCA402998347GAMTc.53C>G (p.Pro18Arg)
19g.1401424G>TCA402998348GAMTc.53C>A (p.Pro18His)
gnomAD v4
19g.1401425G>ACA402998350GAMTc.52C>T (p.Pro18Ser)
gnomAD v4
19g.1401425G>CCA402998351GAMTc.52C>G (p.Pro18Ala)
19g.1401425G>TCA402998352GAMTc.52C>A (p.Pro18Thr)
gnomAD v4
19g.1401426G>ACA504731717GAMTc.51C>T (p.Ser17=)
ClinVar dbSNP gnomAD v4
19g.1401426G>CCA402998354GAMTc.51C>G (p.Ser17Arg)
19g.1401426G=CA2317700451GAMTc.51C= (p.Ser17=)
19g.1401426G>TCA402998353GAMTc.51C>A (p.Ser17Arg)
dbSNP gnomAD v4
19g.1401427delCA2695198107GAMTc.50del (p.Ser17ThrfsTer25)
c.50del (p.Ser17ThrfsTer?)
ClinVar
19g.1401427C>ACA402998357GAMTc.50G>T (p.Ser17Ile)
gnomAD v4
19g.1401427C=CA2317700452GAMTc.50G= (p.Ser17=)
19g.1401427C>GCA402998358GAMTc.50G>C (p.Ser17Thr)
19g.1401427C>TCA304067348GAMTc.50G>A (p.Ser17Asn)
dbSNP gnomAD v3 gnomAD v4
19g.1401428T>ACA402998359GAMTc.49A>T (p.Ser17Cys)
19g.1401428T>CCA402998360GAMTc.49A>G (p.Ser17Gly)
gnomAD v4
19g.1401428T>GCA402998361GAMTc.49A>C (p.Ser17Arg)
gnomAD v4
19g.1401429G>ACA504731722GAMTc.48C>T (p.Cys16=)
gnomAD v4
19g.1401429G>CCA402998363GAMTc.48C>G (p.Cys16Trp)
gnomAD v4
19g.1401429G>TCA402998364GAMTc.48C>A (p.Cys16Ter)
ClinVar gnomAD v4
19g.1401430C>ACA402998365GAMTc.47G>T (p.Cys16Phe)
gnomAD v4
19g.1401430C=CA2317700453GAMTc.47G= (p.Cys16=)
19g.1401430C>GCA402998366GAMTc.47G>C (p.Cys16Ser)
gnomAD v4
19g.1401430C>TCA402998367GAMTc.47G>A (p.Cys16Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.1401431A=CA2317700454GAMTc.46T= (p.Cys16=)
19g.1401431A>CCA402998372GAMTc.46T>G (p.Cys16Gly)
ClinVar dbSNP
19g.1401431A>GCA402998370GAMTc.46T>C (p.Cys16Arg)
gnomAD v4
19g.1401431A>TCA402998369GAMTc.46T>A (p.Cys16Ser)
gnomAD v4
19g.1401432G>ACA504731727GAMTc.45C>T (p.Asn15=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401432G>CCA402998373GAMTc.45C>G (p.Asn15Lys)
19g.1401432G=CA2317700455GAMTc.45C= (p.Asn15=)
19g.1401432G>TCA402998375GAMTc.45C>A (p.Asn15Lys)
gnomAD v4
19g.1401433T>ACA402998377GAMTc.44A>T (p.Asn15Ile)
19g.1401433T>CCA402998378GAMTc.44A>G (p.Asn15Ser)
gnomAD v4
19g.1401433T>GCA402998379GAMTc.44A>C (p.Asn15Thr)
19g.1401434T>ACA402998380GAMTc.43A>T (p.Asn15Tyr)
19g.1401434T>CCA402998381GAMTc.43A>G (p.Asn15Asp)
gnomAD v4
19g.1401434T>GCA402998382GAMTc.43A>C (p.Asn15His)
19g.1401435C>ACA402998384GAMTc.42G>T (p.Glu14Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401435C=CA2317700456GAMTc.42G= (p.Glu14=)
19g.1401435C>GCA9043810GAMTc.42G>C (p.Glu14Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401435C>TCA504731732GAMTc.42G>A (p.Glu14=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401436delCA2576548785GAMTc.41del (p.Glu14GlyfsTer28)
c.41del (p.Glu14GlyfsTer?)
gnomAD v4
19g.1401436T>ACA402998387GAMTc.41A>T (p.Glu14Val)
19g.1401436T>CCA402998388GAMTc.41A>G (p.Glu14Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401436T>GCA402998390GAMTc.41A>C (p.Glu14Ala)
19g.1401436T=CA2317700457GAMTc.41A= (p.Glu14=)
19g.1401437C>ACA402998391GAMTc.40G>T (p.Glu14Ter)
gnomAD v4
19g.1401437C=CA2317700458GAMTc.40G= (p.Glu14=)
19g.1401437C>GCA402998393GAMTc.40G>C (p.Glu14Gln)
gnomAD v4
19g.1401437C>TCA304067351GAMTc.40G>A (p.Glu14Lys)
dbSNP gnomAD v4
19g.1401438G>ACA504731733GAMTc.39C>T (p.Gly13=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401438G>CCA504731734GAMTc.39C>G (p.Gly13=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401438G=CA2317700459GAMTc.39C= (p.Gly13=)
19g.1401438G>TCA504731736GAMTc.39C>A (p.Gly13=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401439C>ACA402998396GAMTc.38G>T (p.Gly13Val)
gnomAD v4
19g.1401439C=CA2317700460GAMTc.38G= (p.Gly13=)
19g.1401439C>GCA402998398GAMTc.38G>C (p.Gly13Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401439C>TCA402998399GAMTc.38G>A (p.Gly13Asp)
gnomAD v4
19g.1401440C>ACA402998401GAMTc.37G>T (p.Gly13Cys)
ClinVar gnomAD v4
19g.1401440C=CA2317700461GAMTc.37G= (p.Gly13=)
19g.1401440C>GCA402998402GAMTc.37G>C (p.Gly13Arg)
dbSNP gnomAD v4
19g.1401440C>TCA402998404GAMTc.37G>A (p.Gly13Ser)
gnomAD v4
19g.1401441G>ACA9043811GAMTc.36C>T (p.Pro12=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401441G>CCA304067356GAMTc.36C>G (p.Pro12=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401441G=CA2317700462GAMTc.36C= (p.Pro12=)
19g.1401441G>TCA504731742GAMTc.36C>A (p.Pro12=)
gnomAD v4
19g.1401443delCA2582641928GAMTc.36del (p.Gly13AlafsTer29)
c.36del (p.Gly13AlafsTer?)
gnomAD v4
19g.1401447_1401472dupCA631301057GAMTc.11_36dup (p.Gly13ProfsTer38)
c.11_36dup (p.Gly13ProfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401442G>ACA402998405GAMTc.35C>T (p.Pro12Leu)
gnomAD v4
19g.1401442G>CCA402998406GAMTc.35C>G (p.Pro12Arg)
19g.1401442G>TCA402998408GAMTc.35C>A (p.Pro12His)
gnomAD v4
19g.1401443G>ACA402998412GAMTc.34C>T (p.Pro12Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401443G>CCA402998411GAMTc.34C>G (p.Pro12Ala)
19g.1401443G=CA2317700463GAMTc.34C= (p.Pro12=)
19g.1401443G>TCA402998409GAMTc.34C>A (p.Pro12Thr)
gnomAD v4
19g.1401446_1401447delCA2813256140GAMTc.33_34del (p.Pro12ArgfsTer?)
19g.1401444C>ACA9043812GAMTc.33G>T (p.Ala11=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401444C=CA2317700464GAMTc.33G= (p.Ala11=)
19g.1401444C>GCA504731744GAMTc.33G>C (p.Ala11=)
19g.1401444C>TCA504731743GAMTc.33G>A (p.Ala11=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401445G>ACA402998418GAMTc.32C>T (p.Ala11Val)
gnomAD v4
19g.1401445G>CCA402998415GAMTc.32C>G (p.Ala11Gly)
19g.1401445G>TCA402998417GAMTc.32C>A (p.Ala11Glu)
gnomAD v4
19g.1401446C>ACA402998419GAMTc.31G>T (p.Ala11Ser)
gnomAD v4
19g.1401446C=CA2317700465GAMTc.31G= (p.Ala11=)
19g.1401446C>GCA402998420GAMTc.31G>C (p.Ala11Pro)
19g.1401446C>TCA402998421GAMTc.31G>A (p.Ala11Thr)
dbSNP gnomAD v4
19g.1401447G>ACA504731746GAMTc.30C>T (p.Phe10=)
gnomAD v4
19g.1401447G>CCA402998422GAMTc.30C>G (p.Phe10Leu)
ClinVar dbSNP
19g.1401447G>TCA402998423GAMTc.30C>A (p.Phe10Leu)
gnomAD v4
19g.1401448A>CCA402998424GAMTc.29T>G (p.Phe10Cys)
19g.1401448A>GCA402998425GAMTc.29T>C (p.Phe10Ser)
gnomAD v4
19g.1401448A>TCA402998426GAMTc.29T>A (p.Phe10Tyr)
19g.1401449delCA2576548786GAMTc.29del (p.Phe10SerfsTer?)
19g.1401449A>CCA402998428GAMTc.28T>G (p.Phe10Val)
19g.1401449A>GCA402998430GAMTc.28T>C (p.Phe10Leu)
gnomAD v4
19g.1401449A>TCA402998432GAMTc.28T>A (p.Phe10Ile)
gnomAD v4
19g.1401450G>ACA504731748GAMTc.27C>T (p.Ile9=)
ClinVar dbSNP gnomAD v4
19g.1401450G>CCA402998434GAMTc.27C>G (p.Ile9Met)
19g.1401450G>TCA504731749GAMTc.27C>A (p.Ile9=)
gnomAD v4
19g.1401451A=CA2317700466GAMTc.26T= (p.Ile9=)
19g.1401451A>CCA402998438GAMTc.26T>G (p.Ile9Ser)
19g.1401451A>GCA402998439GAMTc.26T>C (p.Ile9Thr)
gnomAD v4
19g.1401451A>TCA402998441GAMTc.26T>A (p.Ile9Asn)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401452T>ACA402998444GAMTc.25A>T (p.Ile9Phe)
19g.1401452T>CCA402998450GAMTc.25A>G (p.Ile9Val)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
19g.1401452T>GCA402998451GAMTc.25A>C (p.Ile9Leu)
19g.1401452T=CA2317700468GAMTc.25A= (p.Ile9=)
19g.1401452_1401453delinsTGCA2317700467GAMTc.24_25delinsCA (p.Pro8=)
19g.1401453G>ACA504731750GAMTc.24C>T (p.Pro8=)
gnomAD v4
19g.1401453G>CCA504731751GAMTc.24C>G (p.Pro8=)
19g.1401453G>TCA504731752GAMTc.24C>A (p.Pro8=)
ClinVar dbSNP gnomAD v4
19g.1401457dupCA2813256144GAMTc.24dup (p.Ile9HisfsTer?)
19g.1401456_1401457dupCA2695223170GAMTc.23_24dup (p.Ile9ProfsTer?)
19g.1401457delCA304067361GAMTc.24del (p.Ile9SerfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401454G>ACA402998455GAMTc.23C>T (p.Pro8Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401454G>CCA402998456GAMTc.23C>G (p.Pro8Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401454G=CA2317700469GAMTc.23C= (p.Pro8=)
19g.1401454G>TCA402998460GAMTc.23C>A (p.Pro8His)
gnomAD v4
19g.1401455G>ACA402998463GAMTc.22C>T (p.Pro8Ser)
gnomAD v4
19g.1401455G>CCA402998469GAMTc.22C>G (p.Pro8Ala)
19g.1401455G=CA2317700470GAMTc.22C= (p.Pro8=)
19g.1401455G>TCA314840GAMTc.22C>A (p.Pro8Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401456G>ACA504731753GAMTc.21C>T (p.Thr7=)
dbSNP gnomAD v2 gnomAD v4
19g.1401456G>CCA504731754GAMTc.21C>G (p.Thr7=)
19g.1401456G=CA2317700471GAMTc.21C= (p.Thr7=)
19g.1401456G>TCA504731755GAMTc.21C>A (p.Thr7=)
ClinVar gnomAD v4
19g.1401457G>ACA402998475GAMTc.20C>T (p.Thr7Ile)
gnomAD v4
19g.1401457G>CCA402998477GAMTc.20C>G (p.Thr7Ser)
19g.1401457G=CA2317700472GAMTc.20C= (p.Thr7=)
19g.1401457G>TCA9043813GAMTc.20C>A (p.Thr7Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401458T>ACA402998481GAMTc.19A>T (p.Thr7Ser)
19g.1401458T>CCA402998484GAMTc.19A>G (p.Thr7Ala)
gnomAD v4
19g.1401458T>GCA402998487GAMTc.19A>C (p.Thr7Pro)
gnomAD v3 gnomAD v4
19g.1401459C>ACA504731756GAMTc.18G>T (p.Ala6=)
gnomAD v4
19g.1401459C>GCA504731757GAMTc.18G>C (p.Ala6=)
19g.1401459C>TCA504731758GAMTc.18G>A (p.Ala6=)
ClinVar gnomAD v4
19g.1401460G>ACA314838GAMTc.17C>T (p.Ala6Val)
ClinVar dbSNP gnomAD v4
19g.1401460G>CCA402998490GAMTc.17C>G (p.Ala6Gly)
19g.1401460G=CA2317700473GAMTc.17C= (p.Ala6=)
19g.1401460G>TCA402998491GAMTc.17C>A (p.Ala6Glu)
gnomAD v4
19g.1401461C>ACA402998497GAMTc.16G>T (p.Ala6Ser)
gnomAD v4
19g.1401461C=CA2317700474GAMTc.16G= (p.Ala6=)
19g.1401461C>GCA402998494GAMTc.16G>C (p.Ala6Pro)
19g.1401461C>TCA402998496GAMTc.16G>A (p.Ala6Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401462G>ACA504731759GAMTc.15C>T (p.Ser5=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401462G>CCA402998500GAMTc.15C>G (p.Ser5Arg)
19g.1401462G=CA2317700475GAMTc.15C= (p.Ser5=)
19g.1401462G>TCA402998502GAMTc.15C>A (p.Ser5Arg)
gnomAD v4
19g.1401463C>ACA402998505GAMTc.14G>T (p.Ser5Ile)
gnomAD v4
19g.1401463C>GCA402998506GAMTc.14G>C (p.Ser5Thr)
19g.1401463C>TCA402998509GAMTc.14G>A (p.Ser5Asn)
19g.1401464T>ACA402998512GAMTc.13A>T (p.Ser5Cys)
19g.1401464T>CCA402998516GAMTc.13A>G (p.Ser5Gly)
gnomAD v4
19g.1401464T>GCA402998513GAMTc.13A>C (p.Ser5Arg)
19g.1401465G>ACA504731760GAMTc.12C>T (p.Pro4=)
gnomAD v4
19g.1401465G>CCA504731762GAMTc.12C>G (p.Pro4=)
19g.1401465G>TCA504731761GAMTc.12C>A (p.Pro4=)
gnomAD v4
19g.1401469dupCA2582641929GAMTc.12dup (p.Ser5GlnfsTer?)
gnomAD v4
19g.1401469delCA2582641930GAMTc.12del (p.Ser5AlafsTer?)
gnomAD v4
19g.1401468_1401469delCA2580612592GAMTc.11_12del (p.Pro4GlnfsTer?)
ClinVar
19g.1401466G>ACA304067371GAMTc.11C>T (p.Pro4Leu)
dbSNP gnomAD v4
19g.1401466G>CCA402998527GAMTc.11C>G (p.Pro4Arg)
ClinVar dbSNP
19g.1401466G=CA2317700476GAMTc.11C= (p.Pro4=)
19g.1401466G>TCA402998529GAMTc.11C>A (p.Pro4His)
gnomAD v4
19g.1401467G>ACA304067374GAMTc.10C>T (p.Pro4Ser)
ClinVar dbSNP gnomAD v4
19g.1401467G>CCA402998533GAMTc.10C>G (p.Pro4Ala)
19g.1401467G=CA2317700477GAMTc.10C= (p.Pro4=)
19g.1401467G>TCA402998536GAMTc.10C>A (p.Pro4Thr)
gnomAD v4
19g.1401468G>ACA304067375GAMTc.9C>T (p.Ala3=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401468G>CCA504731763GAMTc.9C>G (p.Ala3=)
19g.1401468G=CA2317700478GAMTc.9C= (p.Ala3=)
19g.1401468G>TCA504731764GAMTc.9C>A (p.Ala3=)
gnomAD v4
19g.1401469G>ACA402998540GAMTc.8C>T (p.Ala3Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401469G>CCA402998541GAMTc.8C>G (p.Ala3Gly)
19g.1401469G=CA2317700479GAMTc.8C= (p.Ala3=)
19g.1401469G>TCA402998545GAMTc.8C>A (p.Ala3Asp)
gnomAD v4
19g.1401470C>ACA314794GAMTc.7G>T (p.Ala3Ser)
ClinVar dbSNP gnomAD v4
19g.1401470C=CA2317700480GAMTc.7G= (p.Ala3=)
19g.1401470C>GCA402998553GAMTc.7G>C (p.Ala3Pro)
gnomAD v4
19g.1401470C>TCA314792GAMTc.7G>A (p.Ala3Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched