Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.229431510_229431534delCA645538675ACTA1c.1021_1045del (p.Ala341AsnfsTer?)
c.964_988del (p.Ala322AsnfsTer?)
c.730_754del (p.Ala244AsnfsTer?)
c.1099_1123del (p.Ala367AsnfsTer?)
COSMIC
1g.229431529G>ACA1442705ACTA1c.1026C>T (p.Gly342=)
c.969C>T (p.Gly323=)
c.735C>T (p.Gly245=)
c.1104C>T (p.Gly368=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.229431529G>CCA423754807ACTA1c.1026C>G (p.Gly342=)
c.969C>G (p.Gly323=)
c.735C>G (p.Gly245=)
c.1104C>G (p.Gly368=)
dbSNP
1g.229431529G=CA1226125370ACTA1c.1026C= (p.Gly342=)
c.969C= (p.Gly323=)
c.735C= (p.Gly245=)
c.1104C= (p.Gly368=)
1g.229431529G>TCA423754806ACTA1c.1026C>A (p.Gly342=)
c.969C>A (p.Gly323=)
c.735C>A (p.Gly245=)
c.1104C>A (p.Gly368=)
1g.229431530C>ACA345144221ACTA1c.1025G>T (p.Gly342Val)
c.968G>T (p.Gly323Val)
c.734G>T (p.Gly245Val)
c.1103G>T (p.Gly368Val)
1g.229431530C>GCA345144224ACTA1c.1025G>C (p.Gly342Ala)
c.968G>C (p.Gly323Ala)
c.734G>C (p.Gly245Ala)
c.1103G>C (p.Gly368Ala)
COSMIC
1g.229431530C>TCA345144226ACTA1c.1025G>A (p.Gly342Asp)
c.968G>A (p.Gly323Asp)
c.734G>A (p.Gly245Asp)
c.1103G>A (p.Gly368Asp)
1g.229431531C>ACA345144227ACTA1c.1024G>T (p.Gly342Cys)
c.967G>T (p.Gly323Cys)
c.733G>T (p.Gly245Cys)
c.1102G>T (p.Gly368Cys)
1g.229431531C>GCA345144229ACTA1c.1024G>C (p.Gly342Arg)
c.967G>C (p.Gly323Arg)
c.733G>C (p.Gly245Arg)
c.1102G>C (p.Gly368Arg)
1g.229431531C>TCA345144231ACTA1c.1024G>A (p.Gly342Ser)
c.967G>A (p.Gly323Ser)
c.733G>A (p.Gly245Ser)
c.1102G>A (p.Gly368Ser)
COSMIC
1g.229431532G>ACA1442706ACTA1c.1023C>T (p.Ala341=)
c.966C>T (p.Ala322=)
c.732C>T (p.Ala244=)
c.1101C>T (p.Ala367=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.229431532G>CCA423754809ACTA1c.1023C>G (p.Ala341=)
c.966C>G (p.Ala322=)
c.732C>G (p.Ala244=)
c.1101C>G (p.Ala367=)
1g.229431532G=CA1226125371ACTA1c.1023C= (p.Ala341=)
c.966C= (p.Ala322=)
c.732C= (p.Ala244=)
c.1101C= (p.Ala367=)
1g.229431532G>TCA423754808ACTA1c.1023C>A (p.Ala341=)
c.966C>A (p.Ala322=)
c.732C>A (p.Ala244=)
c.1101C>A (p.Ala367=)
1g.229431533G>ACA345144235ACTA1c.1022C>T (p.Ala341Val)
c.965C>T (p.Ala322Val)
c.731C>T (p.Ala244Val)
c.1100C>T (p.Ala367Val)
dbSNP gnomAD v2 gnomAD v4
1g.229431533G>CCA345144238ACTA1c.1022C>G (p.Ala341Gly)
c.965C>G (p.Ala322Gly)
c.731C>G (p.Ala244Gly)
c.1100C>G (p.Ala367Gly)
1g.229431533G=CA1226125372ACTA1c.1022C= (p.Ala341=)
c.965C= (p.Ala322=)
c.731C= (p.Ala244=)
c.1100C= (p.Ala367=)
1g.229431533G>TCA345144241ACTA1c.1022C>A (p.Ala341Asp)
c.965C>A (p.Ala322Asp)
c.731C>A (p.Ala244Asp)
c.1100C>A (p.Ala367Asp)
1g.229431534C>ACA345144244ACTA1c.1021G>T (p.Ala341Ser)
c.964G>T (p.Ala322Ser)
c.730G>T (p.Ala244Ser)
c.1099G>T (p.Ala367Ser)
COSMIC
1g.229431534C=CA1226125373ACTA1c.1021G= (p.Ala341=)
c.964G= (p.Ala322=)
c.730G= (p.Ala244=)
c.1099G= (p.Ala367=)
1g.229431534C>GCA345144245ACTA1c.1021G>C (p.Ala341Pro)
c.964G>C (p.Ala322Pro)
c.730G>C (p.Ala244Pro)
c.1099G>C (p.Ala367Pro)
1g.229431534C>TCA345144246ACTA1c.1021G>A (p.Ala341Thr)
c.964G>A (p.Ala322Thr)
c.730G>A (p.Ala244Thr)
c.1099G>A (p.Ala367Thr)
dbSNP gnomAD v2 gnomAD v4
1g.229431535C>ACA345144250ACTA1c.1020G>T (p.Glu340Asp)
c.963G>T (p.Glu321Asp)
c.729G>T (p.Glu243Asp)
c.1098G>T (p.Glu366Asp)
1g.229431535C=CA1226125374ACTA1c.1020G= (p.Glu340=)
c.963G= (p.Glu321=)
c.729G= (p.Glu243=)
c.1098G= (p.Glu366=)
1g.229431535C>GCA345144253ACTA1c.1020G>C (p.Glu340Asp)
c.963G>C (p.Glu321Asp)
c.729G>C (p.Glu243Asp)
c.1098G>C (p.Glu366Asp)
1g.229431535C>TCA423754814ACTA1c.1020G>A (p.Glu340=)
c.963G>A (p.Glu321=)
c.729G>A (p.Glu243=)
c.1098G>A (p.Glu366=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.229431536T>ACA345144256ACTA1c.1019A>T (p.Glu340Val)
c.962A>T (p.Glu321Val)
c.728A>T (p.Glu243Val)
c.1097A>T (p.Glu366Val)
1g.229431536T>CCA345144260ACTA1c.1019A>G (p.Glu340Gly)
c.962A>G (p.Glu321Gly)
c.728A>G (p.Glu243Gly)
c.1097A>G (p.Glu366Gly)
1g.229431536T>GCA345144258ACTA1c.1019A>C (p.Glu340Ala)
c.962A>C (p.Glu321Ala)
c.728A>C (p.Glu243Ala)
c.1097A>C (p.Glu366Ala)
1g.229431537C>ACA345144265ACTA1c.1018G>T (p.Glu340Ter)
c.961G>T (p.Glu321Ter)
c.727G>T (p.Glu243Ter)
c.1096G>T (p.Glu366Ter)
1g.229431537C>GCA345144268ACTA1c.1018G>C (p.Glu340Gln)
c.961G>C (p.Glu321Gln)
c.727G>C (p.Glu243Gln)
c.1096G>C (p.Glu366Gln)
1g.229431537C>TCA345144270ACTA1c.1018G>A (p.Glu340Lys)
c.961G>A (p.Glu321Lys)
c.727G>A (p.Glu243Lys)
c.1096G>A (p.Glu366Lys)
1g.229431538G>ACA1442708ACTA1c.1017C>T (p.Asp339=)
c.960C>T (p.Asp320=)
c.726C>T (p.Asp242=)
c.1095C>T (p.Asp365=)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.229431538G>CCA1442707ACTA1c.1017C>G (p.Asp339Glu)
c.960C>G (p.Asp320Glu)
c.726C>G (p.Asp242Glu)
c.1095C>G (p.Asp365Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.229431538G=CA1143959170ACTA1c.1017C= (p.Asp339=)
c.960C= (p.Asp320=)
c.726C= (p.Asp242=)
c.1095C= (p.Asp365=)
1g.229431538G>TCA345144280ACTA1c.1017C>A (p.Asp339Glu)
c.960C>A (p.Asp320Glu)
c.726C>A (p.Asp242Glu)
c.1095C>A (p.Asp365Glu)
dbSNP gnomAD v3 gnomAD v4
1g.229431539T>ACA345144283ACTA1c.1016A>T (p.Asp339Val)
c.959A>T (p.Asp320Val)
c.725A>T (p.Asp242Val)
c.1094A>T (p.Asp365Val)
1g.229431539T>CCA345144285ACTA1c.1016A>G (p.Asp339Gly)
c.959A>G (p.Asp320Gly)
c.725A>G (p.Asp242Gly)
c.1094A>G (p.Asp365Gly)
1g.229431539T>GCA345144287ACTA1c.1016A>C (p.Asp339Ala)
c.959A>C (p.Asp320Ala)
c.725A>C (p.Asp242Ala)
c.1094A>C (p.Asp365Ala)
1g.229431540delCA2698259255ACTA1c.1015del (p.Asp339ThrfsTer?)
c.958del (p.Asp320ThrfsTer?)
c.724del (p.Asp242ThrfsTer?)
c.1093del (p.Asp365ThrfsTer?)
dbSNP
1g.229431540C>ACA345144291ACTA1c.1015G>T (p.Asp339Tyr)
c.958G>T (p.Asp320Tyr)
c.724G>T (p.Asp242Tyr)
c.1093G>T (p.Asp365Tyr)
1g.229431540C>GCA345144294ACTA1c.1015G>C (p.Asp339His)
c.958G>C (p.Asp320His)
c.724G>C (p.Asp242His)
c.1093G>C (p.Asp365His)
1g.229431540C>TCA345144297ACTA1c.1015G>A (p.Asp339Asn)
c.958G>A (p.Asp320Asn)
c.724G>A (p.Asp242Asn)
c.1093G>A (p.Asp365Asn)
1g.229431540dupCA2650926579ACTA1c.1015dup (p.Asp339GlyfsTer?)
c.958dup (p.Asp320GlyfsTer?)
c.724dup (p.Asp242GlyfsTer?)
c.1093dup (p.Asp365GlyfsTer?)
gnomAD v4
1g.229431541delCA915940544ACTA1c.1014del (p.Tyr338Ter)
c.957del (p.Tyr319Ter)
c.723del (p.Tyr241Ter)
c.1092del (p.Tyr364Ter)
1g.229431541G>ACA38814650ACTA1c.1014C>T (p.Tyr338=)
c.957C>T (p.Tyr319=)
c.723C>T (p.Tyr241=)
c.1092C>T (p.Tyr364=)
dbSNP gnomAD v4
1g.229431541G>CCA345144302ACTA1c.1014C>G (p.Tyr338Ter)
c.957C>G (p.Tyr319Ter)
c.723C>G (p.Tyr241Ter)
c.1092C>G (p.Tyr364Ter)
dbSNP
1g.229431541G=CA1226125375ACTA1c.1014C= (p.Tyr338=)
c.957C= (p.Tyr319=)
c.723C= (p.Tyr241=)
c.1092C= (p.Tyr364=)
1g.229431541G>TCA345144306ACTA1c.1014C>A (p.Tyr338Ter)
c.957C>A (p.Tyr319Ter)
c.723C>A (p.Tyr241Ter)
c.1092C>A (p.Tyr364Ter)

Number of alleles fetched