Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73332176T>ACA491152538HCN4c.1326A>T (p.Leu442=)
c.108A>T (p.Leu36=)
15g.73332176T>CCA491152539HCN4c.1326A>G (p.Leu442=)
c.108A>G (p.Leu36=)
dbSNP
15g.73332176T>GCA491152540HCN4c.1326A>C (p.Leu442=)
c.108A>C (p.Leu36=)
15g.73332176T=CA2187169769HCN4c.1326A= (p.Leu442=)
c.108A= (p.Leu36=)
15g.73332177A>CCA393094339HCN4c.1325T>G (p.Leu442Arg)
c.107T>G (p.Leu36Arg)
15g.73332177A>GCA393094341HCN4c.1325T>C (p.Leu442Pro)
c.107T>C (p.Leu36Pro)
15g.73332177A>TCA393094340HCN4c.1325T>A (p.Leu442Gln)
c.107T>A (p.Leu36Gln)
15g.73332178G>ACA491152541HCN4c.1324C>T (p.Leu442=)
c.106C>T (p.Leu36=)
dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.73332178G>CCA393094342HCN4c.1324C>G (p.Leu442Val)
c.106C>G (p.Leu36Val)
15g.73332178G=CA2187169774HCN4c.1324C= (p.Leu442=)
c.106C= (p.Leu36=)
15g.73332178G>TCA393094343HCN4c.1324C>A (p.Leu442Ile)
c.106C>A (p.Leu36Ile)
15g.73332179C>ACA393094344HCN4c.1323G>T (p.Met441Ile)
c.105G>T (p.Met35Ile)
15g.73332179C>GCA393094345HCN4c.1323G>C (p.Met441Ile)
c.105G>C (p.Met35Ile)
15g.73332179C>TCA393094346HCN4c.1323G>A (p.Met441Ile)
c.105G>A (p.Met35Ile)
gnomAD v4 COSMIC
15g.73332180A>CCA393094347HCN4c.1322T>G (p.Met441Arg)
c.104T>G (p.Met35Arg)
15g.73332180A>GCA393094348HCN4c.1322T>C (p.Met441Thr)
c.104T>C (p.Met35Thr)
15g.73332180A>TCA393094349HCN4c.1322T>A (p.Met441Lys)
c.104T>A (p.Met35Lys)
15g.73332181T>ACA393094350HCN4c.1321A>T (p.Met441Leu)
c.103A>T (p.Met35Leu)
15g.73332181T>CCA7649326HCN4c.1321A>G (p.Met441Val)
c.103A>G (p.Met35Val)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332181T>GCA393094351HCN4c.1321A>C (p.Met441Leu)
c.103A>C (p.Met35Leu)
15g.73332181T=CA2187169779HCN4c.1321A= (p.Met441=)
c.103A= (p.Met35=)
15g.73332182G>ACA491152542HCN4c.1320C>T (p.Pro440=)
c.102C>T (p.Pro34=)
15g.73332182G>CCA491152543HCN4c.1320C>G (p.Pro440=)
c.102C>G (p.Pro34=)
15g.73332182G>TCA491152544HCN4c.1320C>A (p.Pro440=)
c.102C>A (p.Pro34=)
15g.73332183G>ACA393094353HCN4c.1319C>T (p.Pro440Leu)
c.101C>T (p.Pro34Leu)
gnomAD v4
15g.73332183G>CCA393094354HCN4c.1319C>G (p.Pro440Arg)
c.101C>G (p.Pro34Arg)
15g.73332183G>TCA393094352HCN4c.1319C>A (p.Pro440His)
c.101C>A (p.Pro34His)
15g.73332184G>ACA393094355HCN4c.1318C>T (p.Pro440Ser)
c.100C>T (p.Pro34Ser)
dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.73332184G>CCA393094356HCN4c.1318C>G (p.Pro440Ala)
c.100C>G (p.Pro34Ala)
15g.73332184G=CA2187169781HCN4c.1318C= (p.Pro440=)
c.100C= (p.Pro34=)
15g.73332184G>TCA393094357HCN4c.1318C>A (p.Pro440Thr)
c.100C>A (p.Pro34Thr)
15g.73332185T>ACA491152547HCN4c.1317A>T (p.Val439=)
c.99A>T (p.Val33=)
15g.73332185T>CCA491152546HCN4c.1317A>G (p.Val439=)
c.99A>G (p.Val33=)
15g.73332185T>GCA491152545HCN4c.1317A>C (p.Val439=)
c.99A>C (p.Val33=)
15g.73332186A>CCA393094358HCN4c.1316T>G (p.Val439Gly)
c.98T>G (p.Val33Gly)
15g.73332186A>GCA393094359HCN4c.1316T>C (p.Val439Ala)
c.98T>C (p.Val33Ala)
gnomAD v4
15g.73332186A>TCA393094360HCN4c.1316T>A (p.Val439Glu)
c.98T>A (p.Val33Glu)
15g.73332187C>ACA393094361HCN4c.1315G>T (p.Val439Leu)
c.97G>T (p.Val33Leu)
15g.73332187C=CA2187169785HCN4c.1315G= (p.Val439=)
c.97G= (p.Val33=)
15g.73332187C>GCA7649327HCN4c.1315G>C (p.Val439Leu)
c.97G>C (p.Val33Leu)
ClinVar dbSNP ExAC
15g.73332187C>TCA393094362HCN4c.1315G>A (p.Val439Ile)
c.97G>A (p.Val33Ile)
ClinVar
15g.73332188C>ACA491152550HCN4c.1314G>T (p.Leu438=)
c.96G>T (p.Leu32=)
15g.73332188C>GCA491152549HCN4c.1314G>C (p.Leu438=)
c.96G>C (p.Leu32=)
15g.73332188C>TCA491152548HCN4c.1314G>A (p.Leu438=)
c.96G>A (p.Leu32=)
gnomAD v4
15g.73332189A>CCA393094363HCN4c.1313T>G (p.Leu438Arg)
c.95T>G (p.Leu32Arg)
15g.73332189A>GCA393094364HCN4c.1313T>C (p.Leu438Pro)
c.95T>C (p.Leu32Pro)
15g.73332189A>TCA393094365HCN4c.1313T>A (p.Leu438Gln)
c.95T>A (p.Leu32Gln)
15g.73332190G>ACA491152551HCN4c.1312C>T (p.Leu438=)
c.94C>T (p.Leu32=)
ClinVar dbSNP
15g.73332190G>CCA393094366HCN4c.1312C>G (p.Leu438Val)
c.94C>G (p.Leu32Val)
15g.73332190G=CA2187169789HCN4c.1312C= (p.Leu438=)
c.94C= (p.Leu32=)
15g.73332190G>TCA393094367HCN4c.1312C>A (p.Leu438Met)
c.94C>A (p.Leu32Met)
15g.73332191G>ACA491152552HCN4c.1311C>T (p.Phe437=)
c.93C>T (p.Phe31=)
15g.73332191G>CCA393094369HCN4c.1311C>G (p.Phe437Leu)
c.93C>G (p.Phe31Leu)
15g.73332191G>TCA393094368HCN4c.1311C>A (p.Phe437Leu)
c.93C>A (p.Phe31Leu)
15g.73332192A>CCA393094370HCN4c.1310T>G (p.Phe437Cys)
c.92T>G (p.Phe31Cys)
15g.73332192A>GCA393094371HCN4c.1310T>C (p.Phe437Ser)
c.92T>C (p.Phe31Ser)
15g.73332192A>TCA393094372HCN4c.1310T>A (p.Phe437Tyr)
c.92T>A (p.Phe31Tyr)
15g.73332193A>CCA393094373HCN4c.1309T>G (p.Phe437Val)
c.91T>G (p.Phe31Val)
15g.73332193A>GCA393094374HCN4c.1309T>C (p.Phe437Leu)
c.91T>C (p.Phe31Leu)
15g.73332193A>TCA393094375HCN4c.1309T>A (p.Phe437Ile)
c.91T>A (p.Phe31Ile)
15g.73332194C>ACA393094377HCN4c.1308G>T (p.Gln436His)
c.90G>T (p.Gln30His)
ClinVar dbSNP COSMIC
15g.73332194C=CA2187169791HCN4c.1308G= (p.Gln436=)
c.90G= (p.Gln30=)
15g.73332194C>GCA393094376HCN4c.1308G>C (p.Gln436His)
c.90G>C (p.Gln30His)
15g.73332194C>TCA491152553HCN4c.1308G>A (p.Gln436=)
c.90G>A (p.Gln30=)
ClinVar dbSNP
15g.73332195T>ACA393094378HCN4c.1307A>T (p.Gln436Leu)
c.89A>T (p.Gln30Leu)
15g.73332195T>CCA393094379HCN4c.1307A>G (p.Gln436Arg)
c.89A>G (p.Gln30Arg)
15g.73332195T>GCA393094380HCN4c.1307A>C (p.Gln436Pro)
c.89A>C (p.Gln30Pro)
15g.73332196G>ACA393094381HCN4c.1306C>T (p.Gln436Ter)
c.88C>T (p.Gln30Ter)
15g.73332196G>CCA393094382HCN4c.1306C>G (p.Gln436Glu)
c.88C>G (p.Gln30Glu)
15g.73332196G>TCA393094383HCN4c.1306C>A (p.Gln436Lys)
c.88C>A (p.Gln30Lys)
15g.73332197C>ACA491152555HCN4c.1305G>T (p.Leu435=)
c.87G>T (p.Leu29=)
15g.73332197C>GCA491152556HCN4c.1305G>C (p.Leu435=)
c.87G>C (p.Leu29=)
15g.73332197C>TCA491152557HCN4c.1305G>A (p.Leu435=)
c.87G>A (p.Leu29=)
15g.73332198A=CA2187169796HCN4c.1304T= (p.Leu435=)
c.86T= (p.Leu29=)
15g.73332198A>CCA393094385HCN4c.1304T>G (p.Leu435Arg)
c.86T>G (p.Leu29Arg)
15g.73332198A>GCA7649328HCN4c.1304T>C (p.Leu435Pro)
c.86T>C (p.Leu29Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332198A>TCA393094384HCN4c.1304T>A (p.Leu435Gln)
c.86T>A (p.Leu29Gln)
15g.73332199G>ACA7649329HCN4c.1303C>T (p.Leu435=)
c.85C>T (p.Leu29=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332199G>CCA393094386HCN4c.1303C>G (p.Leu435Val)
c.85C>G (p.Leu29Val)
15g.73332199G=CA2187169798HCN4c.1303C= (p.Leu435=)
c.85C= (p.Leu29=)
15g.73332199G>TCA393094387HCN4c.1303C>A (p.Leu435Met)
c.85C>A (p.Leu29Met)
15g.73332200G>ACA491152559HCN4c.1302C>T (p.Cys434=)
c.84C>T (p.Cys28=)
15g.73332200G>CCA393094388HCN4c.1302C>G (p.Cys434Trp)
c.84C>G (p.Cys28Trp)
15g.73332200G>TCA393094389HCN4c.1302C>A (p.Cys434Ter)
c.84C>A (p.Cys28Ter)
15g.73332201C>ACA393094392HCN4c.1301G>T (p.Cys434Phe)
c.83G>T (p.Cys28Phe)
15g.73332201C>GCA393094391HCN4c.1301G>C (p.Cys434Ser)
c.83G>C (p.Cys28Ser)
15g.73332201C>TCA393094390HCN4c.1301G>A (p.Cys434Tyr)
c.83G>A (p.Cys28Tyr)
15g.73332202A>CCA393094393HCN4c.1300T>G (p.Cys434Gly)
c.82T>G (p.Cys28Gly)
15g.73332202A>GCA393094394HCN4c.1300T>C (p.Cys434Arg)
c.82T>C (p.Cys28Arg)
15g.73332202A>TCA393094395HCN4c.1300T>A (p.Cys434Ser)
c.82T>A (p.Cys28Ser)
15g.73332203G>ACA491152560HCN4c.1299C>T (p.Gly433=)
c.81C>T (p.Gly27=)
15g.73332203G>CCA491152561HCN4c.1299C>G (p.Gly433=)
c.81C>G (p.Gly27=)
15g.73332203G>TCA491152563HCN4c.1299C>A (p.Gly433=)
c.81C>A (p.Gly27=)
15g.73332204C>ACA393094396HCN4c.1298G>T (p.Gly433Val)
c.80G>T (p.Gly27Val)
15g.73332204C>GCA393094397HCN4c.1298G>C (p.Gly433Ala)
c.80G>C (p.Gly27Ala)
15g.73332204C>TCA393094398HCN4c.1298G>A (p.Gly433Asp)
c.80G>A (p.Gly27Asp)
15g.73332205C>ACA393094399HCN4c.1297G>T (p.Gly433Cys)
c.79G>T (p.Gly27Cys)
15g.73332205C=CA2187169804HCN4c.1297G= (p.Gly433=)
c.79G= (p.Gly27=)
15g.73332205C>GCA393094400HCN4c.1297G>C (p.Gly433Arg)
c.79G>C (p.Gly27Arg)
15g.73332205C>TCA7649330HCN4c.1297G>A (p.Gly433Ser)
c.79G>A (p.Gly27Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332206G>ACA491152567HCN4c.1296C>T (p.Asp432=)
c.78C>T (p.Asp26=)
ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73332206G>CCA393094401HCN4c.1296C>G (p.Asp432Glu)
c.78C>G (p.Asp26Glu)
15g.73332206G=CA2187169810HCN4c.1296C= (p.Asp432=)
c.78C= (p.Asp26=)
15g.73332206G>TCA393094402HCN4c.1296C>A (p.Asp432Glu)
c.78C>A (p.Asp26Glu)
15g.73332207T>ACA393094403HCN4c.1295A>T (p.Asp432Val)
c.77A>T (p.Asp26Val)
15g.73332207T>CCA393094404HCN4c.1295A>G (p.Asp432Gly)
c.77A>G (p.Asp26Gly)
15g.73332207T>GCA393094405HCN4c.1295A>C (p.Asp432Ala)
c.77A>C (p.Asp26Ala)
15g.73332208C>ACA393094406HCN4c.1294G>T (p.Asp432Tyr)
c.76G>T (p.Asp26Tyr)
15g.73332208C>GCA393094407HCN4c.1294G>C (p.Asp432His)
c.76G>C (p.Asp26His)
15g.73332208C>TCA393094408HCN4c.1294G>A (p.Asp432Asn)
c.76G>A (p.Asp26Asn)
15g.73332210delCA2575783969HCN4c.1294del (p.Asp432ThrfsTer26)
c.76del (p.Asp26ThrfsTer26)
15g.73332209C>ACA393094409HCN4c.1293G>T (p.Trp431Cys)
c.75G>T (p.Trp25Cys)
15g.73332209C>GCA393094410HCN4c.1293G>C (p.Trp431Cys)
c.75G>C (p.Trp25Cys)
15g.73332209C>TCA393094411HCN4c.1293G>A (p.Trp431Ter)
c.75G>A (p.Trp25Ter)
15g.73332210C>ACA393094412HCN4c.1292G>T (p.Trp431Leu)
c.74G>T (p.Trp25Leu)
15g.73332210C>GCA393094414HCN4c.1292G>C (p.Trp431Ser)
c.74G>C (p.Trp25Ser)
15g.73332210C>TCA393094413HCN4c.1292G>A (p.Trp431Ter)
c.74G>A (p.Trp25Ter)
gnomAD v4
15g.73332211A>CCA393094415HCN4c.1291T>G (p.Trp431Gly)
c.73T>G (p.Trp25Gly)
15g.73332211A>GCA393094417HCN4c.1291T>C (p.Trp431Arg)
c.73T>C (p.Trp25Arg)
15g.73332211A>TCA393094416HCN4c.1291T>A (p.Trp431Arg)
c.73T>A (p.Trp25Arg)
15g.73332212G>ACA272673937HCN4c.1290C>T (p.His430=)
c.72C>T (p.His24=)
ClinVar dbSNP gnomAD v4
15g.73332212G>CCA393094418HCN4c.1290C>G (p.His430Gln)
c.72C>G (p.His24Gln)
COSMIC
15g.73332212G=CA2187169814HCN4c.1290C= (p.His430=)
c.72C= (p.His24=)
15g.73332212G>TCA393094419HCN4c.1290C>A (p.His430Gln)
c.72C>A (p.His24Gln)
15g.73332213T>ACA393094420HCN4c.1289A>T (p.His430Leu)
c.71A>T (p.His24Leu)
15g.73332213T>CCA393094421HCN4c.1289A>G (p.His430Arg)
c.71A>G (p.His24Arg)
15g.73332213T>GCA393094422HCN4c.1289A>C (p.His430Pro)
c.71A>C (p.His24Pro)
15g.73332214G>ACA393094423HCN4c.1288C>T (p.His430Tyr)
c.70C>T (p.His24Tyr)
15g.73332214G>CCA393094424HCN4c.1288C>G (p.His430Asp)
c.70C>G (p.His24Asp)
15g.73332214G>TCA393094425HCN4c.1288C>A (p.His430Asn)
c.70C>A (p.His24Asn)
15g.73332215G>ACA491152574HCN4c.1287C>T (p.Cys429=)
c.69C>T (p.Cys23=)
15g.73332215G>CCA393094426HCN4c.1287C>G (p.Cys429Trp)
c.69C>G (p.Cys23Trp)
15g.73332215G>TCA393094427HCN4c.1287C>A (p.Cys429Ter)
c.69C>A (p.Cys23Ter)
15g.73332216C>ACA393094430HCN4c.1286G>T (p.Cys429Phe)
c.68G>T (p.Cys23Phe)
15g.73332216C>GCA393094428HCN4c.1286G>C (p.Cys429Ser)
c.68G>C (p.Cys23Ser)
15g.73332216C>TCA393094429HCN4c.1286G>A (p.Cys429Tyr)
c.68G>A (p.Cys23Tyr)
15g.73332217A>CCA393094431HCN4c.1285T>G (p.Cys429Gly)
c.67T>G (p.Cys23Gly)
15g.73332217A>GCA393094432HCN4c.1285T>C (p.Cys429Arg)
c.67T>C (p.Cys23Arg)
15g.73332217A>TCA393094433HCN4c.1285T>A (p.Cys429Ser)
c.67T>A (p.Cys23Ser)
15g.73332218G>ACA7649331HCN4c.1284C>T (p.Leu428=)
c.66C>T (p.Leu22=)
ClinVar dbSNP ExAC gnomAD v2
15g.73332218G>CCA491152579HCN4c.1284C>G (p.Leu428=)
c.66C>G (p.Leu22=)
dbSNP gnomAD v2 gnomAD v4
15g.73332218G=CA2187169819HCN4c.1284C= (p.Leu428=)
c.66C= (p.Leu22=)
15g.73332218G>TCA491152580HCN4c.1284C>A (p.Leu428=)
c.66C>A (p.Leu22=)
15g.73332219A=CA2187169821HCN4c.1283T= (p.Leu428=)
c.65T= (p.Leu22=)
15g.73332219A>CCA393094434HCN4c.1283T>G (p.Leu428Arg)
c.65T>G (p.Leu22Arg)
15g.73332219A>GCA393094435HCN4c.1283T>C (p.Leu428Pro)
c.65T>C (p.Leu22Pro)
dbSNP gnomAD v4
15g.73332219A>TCA393094436HCN4c.1283T>A (p.Leu428His)
c.65T>A (p.Leu22His)
15g.73332220G>ACA393094437HCN4c.1282C>T (p.Leu428Phe)
c.64C>T (p.Leu22Phe)
15g.73332220G>CCA393094438HCN4c.1282C>G (p.Leu428Val)
c.64C>G (p.Leu22Val)
15g.73332220G>TCA393094439HCN4c.1282C>A (p.Leu428Ile)
c.64C>A (p.Leu22Ile)
15g.73332221C>ACA491152582HCN4c.1281G>T (p.Leu427=)
c.63G>T (p.Leu21=)
ClinVar gnomAD v4
15g.73332221C>GCA491152583HCN4c.1281G>C (p.Leu427=)
c.63G>C (p.Leu21=)
15g.73332221C>TCA491152584HCN4c.1281G>A (p.Leu427=)
c.63G>A (p.Leu21=)
15g.73332222A>CCA393094441HCN4c.1280T>G (p.Leu427Arg)
c.62T>G (p.Leu21Arg)
15g.73332222A>GCA393094442HCN4c.1280T>C (p.Leu427Pro)
c.62T>C (p.Leu21Pro)
15g.73332222A>TCA393094440HCN4c.1280T>A (p.Leu427Gln)
c.62T>A (p.Leu21Gln)
15g.73332223G>ACA491152586HCN4c.1279C>T (p.Leu427=)
c.61C>T (p.Leu21=)
15g.73332223G>CCA393094443HCN4c.1279C>G (p.Leu427Val)
c.61C>G (p.Leu21Val)
15g.73332223G>TCA393094444HCN4c.1279C>A (p.Leu427Met)
c.61C>A (p.Leu21Met)
15g.73332224delCA2629388815HCN4c.1279del (p.Leu427CysfsTer?)
c.61del (p.Leu21CysfsTer?)
gnomAD v4
15g.73332224G>ACA491152587HCN4c.1278C>T (p.Leu426=)
c.60C>T (p.Leu20=)
ClinVar COSMIC
15g.73332224G>CCA7649332HCN4c.1278C>G (p.Leu426=)
c.60C>G (p.Leu20=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332224G=CA2187169823HCN4c.1278C= (p.Leu426=)
c.60C= (p.Leu20=)
15g.73332224G>TCA491152589HCN4c.1278C>A (p.Leu426=)
c.60C>A (p.Leu20=)
15g.73332225A>CCA393094445HCN4c.1277T>G (p.Leu426Arg)
c.59T>G (p.Leu20Arg)
15g.73332225A>GCA393094446HCN4c.1277T>C (p.Leu426Pro)
c.59T>C (p.Leu20Pro)
15g.73332225A>TCA393094447HCN4c.1277T>A (p.Leu426His)
c.59T>A (p.Leu20His)
15g.73332226G>ACA393094448HCN4c.1276C>T (p.Leu426Phe)
c.58C>T (p.Leu20Phe)
15g.73332226G>CCA393094449HCN4c.1276C>G (p.Leu426Val)
c.58C>G (p.Leu20Val)
15g.73332226G>TCA393094450HCN4c.1276C>A (p.Leu426Ile)
c.58C>A (p.Leu20Ile)
15g.73332227C>ACA393094451HCN4c.1275G>T (p.Met425Ile)
c.57G>T (p.Met19Ile)
15g.73332227C>GCA393094452HCN4c.1275G>C (p.Met425Ile)
c.57G>C (p.Met19Ile)
15g.73332227C>TCA393094453HCN4c.1275G>A (p.Met425Ile)
c.57G>A (p.Met19Ile)
15g.73332228A>CCA393094456HCN4c.1274T>G (p.Met425Arg)
c.56T>G (p.Met19Arg)
15g.73332228A>GCA393094454HCN4c.1274T>C (p.Met425Thr)
c.56T>C (p.Met19Thr)
gnomAD v4
15g.73332228A>TCA393094455HCN4c.1274T>A (p.Met425Lys)
c.56T>A (p.Met19Lys)
15g.73332229T>ACA393094457HCN4c.1273A>T (p.Met425Leu)
c.55A>T (p.Met19Leu)
15g.73332229T>CCA393094458HCN4c.1273A>G (p.Met425Val)
c.55A>G (p.Met19Val)
15g.73332229T>GCA393094459HCN4c.1273A>C (p.Met425Leu)
c.55A>C (p.Met19Leu)
15g.73332230C>ACA393094460HCN4c.1272G>T (p.Met424Ile)
c.54G>T (p.Met18Ile)
gnomAD v4
15g.73332230C>GCA393094461HCN4c.1272G>C (p.Met424Ile)
c.54G>C (p.Met18Ile)
15g.73332230C>TCA393094462HCN4c.1272G>A (p.Met424Ile)
c.54G>A (p.Met18Ile)
gnomAD v4
15g.73332231A>CCA393094463HCN4c.1271T>G (p.Met424Arg)
c.53T>G (p.Met18Arg)
15g.73332231A>GCA393094464HCN4c.1271T>C (p.Met424Thr)
c.53T>C (p.Met18Thr)
15g.73332231A>TCA393094465HCN4c.1271T>A (p.Met424Lys)
c.53T>A (p.Met18Lys)
15g.73332232T>ACA393094466HCN4c.1270A>T (p.Met424Leu)
c.52A>T (p.Met18Leu)
15g.73332232T>CCA393094467HCN4c.1270A>G (p.Met424Val)
c.52A>G (p.Met18Val)
15g.73332232T>GCA393094468HCN4c.1270A>C (p.Met424Leu)
c.52A>C (p.Met18Leu)
15g.73332233G>ACA491152597HCN4c.1269C>T (p.Gly423=)
c.51C>T (p.Gly17=)
15g.73332233G>CCA491152598HCN4c.1269C>G (p.Gly423=)
c.51C>G (p.Gly17=)
15g.73332233G>TCA491152599HCN4c.1269C>A (p.Gly423=)
c.51C>A (p.Gly17=)
15g.73332234C>ACA393094471HCN4c.1268G>T (p.Gly423Val)
c.50G>T (p.Gly17Val)
15g.73332234C>GCA393094470HCN4c.1268G>C (p.Gly423Ala)
c.50G>C (p.Gly17Ala)
15g.73332234C>TCA393094469HCN4c.1268G>A (p.Gly423Asp)
c.50G>A (p.Gly17Asp)
15g.73332235C>ACA393094472HCN4c.1267G>T (p.Gly423Cys)
c.49G>T (p.Gly17Cys)
15g.73332235C=CA2187169826HCN4c.1267G= (p.Gly423=)
c.49G= (p.Gly17=)
15g.73332235C>GCA393094473HCN4c.1267G>C (p.Gly423Arg)
c.49G>C (p.Gly17Arg)
15g.73332235C>TCA7649333HCN4c.1267G>A (p.Gly423Ser)
c.49G>A (p.Gly17Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332236G>ACA7649334HCN4c.1266C>T (p.Ile422=)
c.48C>T (p.Ile16=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
15g.73332236G>CCA393094474HCN4c.1266C>G (p.Ile422Met)
c.48C>G (p.Ile16Met)
15g.73332236G=CA2187169828HCN4c.1266C= (p.Ile422=)
c.48C= (p.Ile16=)
15g.73332236G>TCA491152603HCN4c.1266C>A (p.Ile422=)
c.48C>A (p.Ile16=)
15g.73332237A>CCA393094475HCN4c.1265T>G (p.Ile422Ser)
c.47T>G (p.Ile16Ser)
15g.73332237A>GCA393094477HCN4c.1265T>C (p.Ile422Thr)
c.47T>C (p.Ile16Thr)
15g.73332237A>TCA393094476HCN4c.1265T>A (p.Ile422Asn)
c.47T>A (p.Ile16Asn)
15g.73332238T>ACA393094478HCN4c.1264A>T (p.Ile422Phe)
c.46A>T (p.Ile16Phe)
15g.73332238T>CCA393094479HCN4c.1264A>G (p.Ile422Val)
c.46A>G (p.Ile16Val)
15g.73332238T>GCA393094480HCN4c.1264A>C (p.Ile422Leu)
c.46A>C (p.Ile16Leu)
15g.73332239G>ACA491152605HCN4c.1263C>T (p.Leu421=)
c.45C>T (p.Leu15=)
15g.73332239G>CCA491152607HCN4c.1263C>G (p.Leu421=)
c.45C>G (p.Leu15=)
15g.73332239G>TCA491152606HCN4c.1263C>A (p.Leu421=)
c.45C>A (p.Leu15=)
15g.73332240A>CCA393094481HCN4c.1262T>G (p.Leu421Arg)
c.44T>G (p.Leu15Arg)
15g.73332240A>GCA393094482HCN4c.1262T>C (p.Leu421Pro)
c.44T>C (p.Leu15Pro)
15g.73332240A>TCA393094483HCN4c.1262T>A (p.Leu421His)
c.44T>A (p.Leu15His)
15g.73332241G>ACA393094484HCN4c.1261C>T (p.Leu421Phe)
c.43C>T (p.Leu15Phe)
15g.73332241G>CCA393094485HCN4c.1261C>G (p.Leu421Val)
c.43C>G (p.Leu15Val)
15g.73332241G>TCA393094486HCN4c.1261C>A (p.Leu421Ile)
c.43C>A (p.Leu15Ile)
15g.73332242G>ACA491152611HCN4c.1260C>T (p.Asn420=)
c.42C>T (p.Asn14=)
gnomAD v4
15g.73332242G>CCA393094487HCN4c.1260C>G (p.Asn420Lys)
c.42C>G (p.Asn14Lys)
15g.73332242G>TCA393094488HCN4c.1260C>A (p.Asn420Lys)
c.42C>A (p.Asn14Lys)
15g.73332243T>ACA393094491HCN4c.1259A>T (p.Asn420Ile)
c.41A>T (p.Asn14Ile)
15g.73332243T>CCA393094489HCN4c.1259A>G (p.Asn420Ser)
c.41A>G (p.Asn14Ser)
15g.73332243T>GCA393094490HCN4c.1259A>C (p.Asn420Thr)
c.41A>C (p.Asn14Thr)
dbSNP
15g.73332243T=CA2187169831HCN4c.1259A= (p.Asn420=)
c.41A= (p.Asn14=)
15g.73332244T>ACA393094492HCN4c.1258A>T (p.Asn420Tyr)
c.40A>T (p.Asn14Tyr)
15g.73332244T>CCA393094493HCN4c.1258A>G (p.Asn420Asp)
c.40A>G (p.Asn14Asp)
15g.73332244T>GCA393094494HCN4c.1258A>C (p.Asn420His)
c.40A>C (p.Asn14His)
15g.73332245C>ACA7649335HCN4c.1257G>T (p.Val419=)
c.39G>T (p.Val13=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332245C=CA2187169834HCN4c.1257G= (p.Val419=)
c.39G= (p.Val13=)
15g.73332245C>GCA491152616HCN4c.1257G>C (p.Val419=)
c.39G>C (p.Val13=)
gnomAD v4
15g.73332245C>TCA491152617HCN4c.1257G>A (p.Val419=)
c.39G>A (p.Val13=)
COSMIC
15g.73332246A>CCA393094495HCN4c.1256T>G (p.Val419Gly)
c.38T>G (p.Val13Gly)
ClinVar
15g.73332246A>GCA393094496HCN4c.1256T>C (p.Val419Ala)
c.38T>C (p.Val13Ala)
gnomAD v4
15g.73332246A>TCA393094497HCN4c.1256T>A (p.Val419Glu)
c.38T>A (p.Val13Glu)
15g.73332247C>ACA393094498HCN4c.1255G>T (p.Val419Leu)
c.37G>T (p.Val13Leu)
15g.73332247C=CA2187169837HCN4c.1255G= (p.Val419=)
c.37G= (p.Val13=)
15g.73332247C>GCA393094499HCN4c.1255G>C (p.Val419Leu)
c.37G>C (p.Val13Leu)
15g.73332247C>TCA393094500HCN4c.1255G>A (p.Val419Met)
c.37G>A (p.Val13Met)
ClinVar dbSNP gnomAD v4 COSMIC
15g.73332248G>ACA7649336HCN4c.1254C>T (p.Ile418=)
c.36C>T (p.Ile12=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332248G>CCA393094501HCN4c.1254C>G (p.Ile418Met)
c.36C>G (p.Ile12Met)
15g.73332248G=CA2187169842HCN4c.1254C= (p.Ile418=)
c.36C= (p.Ile12=)
15g.73332248G>TCA491152619HCN4c.1254C>A (p.Ile418=)
c.36C>A (p.Ile12=)
COSMIC
15g.73332249A>CCA393094502HCN4c.1253T>G (p.Ile418Ser)
c.35T>G (p.Ile12Ser)
15g.73332249A>GCA393094503HCN4c.1253T>C (p.Ile418Thr)
c.35T>C (p.Ile12Thr)
15g.73332249A>TCA393094504HCN4c.1253T>A (p.Ile418Asn)
c.35T>A (p.Ile12Asn)
15g.73332250T>ACA393094505HCN4c.1252A>T (p.Ile418Phe)
c.34A>T (p.Ile12Phe)
gnomAD v4
15g.73332250T>CCA393094506HCN4c.1252A>G (p.Ile418Val)
c.34A>G (p.Ile12Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73332250T>GCA393094507HCN4c.1252A>C (p.Ile418Leu)
c.34A>C (p.Ile12Leu)
15g.73332250T=CA2187169847HCN4c.1252A= (p.Ile418=)
c.34A= (p.Ile12=)
15g.73332251G>ACA491152620HCN4c.1251C>T (p.Arg417=)
c.33C>T (p.Arg11=)
gnomAD v4
15g.73332251G>CCA491152623HCN4c.1251C>G (p.Arg417=)
c.33C>G (p.Arg11=)
15g.73332251G>TCA491152621HCN4c.1251C>A (p.Arg417=)
c.33C>A (p.Arg11=)
15g.73332252C>ACA393094508HCN4c.1250G>T (p.Arg417Leu)
c.32G>T (p.Arg11Leu)
15g.73332252C=CA2187169849HCN4c.1250G= (p.Arg417=)
c.32G= (p.Arg11=)
15g.73332252C>GCA393094509HCN4c.1250G>C (p.Arg417Pro)
c.32G>C (p.Arg11Pro)
15g.73332252C>TCA272673953HCN4c.1250G>A (p.Arg417His)
c.32G>A (p.Arg11His)
ClinVar dbSNP gnomAD v4 COSMIC
15g.73332253G>ACA393094510HCN4c.1249C>T (p.Arg417Cys)
c.31C>T (p.Arg11Cys)
15g.73332253G>CCA7649337HCN4c.1249C>G (p.Arg417Gly)
c.31C>G (p.Arg11Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332253G=CA2187169854HCN4c.1249C= (p.Arg417=)
c.31C= (p.Arg11=)
15g.73332253G>TCA393094511HCN4c.1249C>A (p.Arg417Ser)
c.31C>A (p.Arg11Ser)
15g.73332254C>ACA491152625HCN4c.1248G>T (p.Val416=)
c.30G>T (p.Val10=)
15g.73332254C>GCA491152627HCN4c.1248G>C (p.Val416=)
c.30G>C (p.Val10=)
15g.73332254C>TCA491152628HCN4c.1248G>A (p.Val416=)
c.30G>A (p.Val10=)
ClinVar
15g.73332255A>CCA393094514HCN4c.1247T>G (p.Val416Gly)
c.29T>G (p.Val10Gly)
15g.73332255A>GCA393094513HCN4c.1247T>C (p.Val416Ala)
c.29T>C (p.Val10Ala)
15g.73332255A>TCA393094512HCN4c.1247T>A (p.Val416Glu)
c.29T>A (p.Val10Glu)
dbSNP
15g.73332256C>ACA393094515HCN4c.1246G>T (p.Val416Leu)
c.28G>T (p.Val10Leu)
ClinVar dbSNP
15g.73332256C=CA2187169857HCN4c.1246G= (p.Val416=)
c.28G= (p.Val10=)
15g.73332256C>GCA393094516HCN4c.1246G>C (p.Val416Leu)
c.28G>C (p.Val10Leu)
dbSNP
15g.73332256C>TCA393094517HCN4c.1246G>A (p.Val416Met)
c.28G>A (p.Val10Met)
gnomAD v4
15g.73332257C>ACA491152630HCN4c.1245G>T (p.Val415=)
c.27G>T (p.Val9=)
15g.73332257C>GCA491152631HCN4c.1245G>C (p.Val415=)
c.27G>C (p.Val9=)
15g.73332257C>TCA491152633HCN4c.1245G>A (p.Val415=)
c.27G>A (p.Val9=)
15g.73332258A>CCA393094518HCN4c.1244T>G (p.Val415Gly)
c.26T>G (p.Val9Gly)
15g.73332258A>GCA393094519HCN4c.1244T>C (p.Val415Ala)
c.26T>C (p.Val9Ala)
15g.73332258A>TCA393094520HCN4c.1244T>A (p.Val415Glu)
c.26T>A (p.Val9Glu)
15g.73332259C>ACA393094521HCN4c.1243G>T (p.Val415Leu)
c.25G>T (p.Val9Leu)
15g.73332259C=CA2187169866HCN4c.1243G= (p.Val415=)
c.25G= (p.Val9=)
15g.73332259C>GCA393094522HCN4c.1243G>C (p.Val415Leu)
c.25G>C (p.Val9Leu)
15g.73332259C>TCA7649338HCN4c.1243G>A (p.Val415Met)
c.25G>A (p.Val9Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332260G>ACA7649339HCN4c.1242C>T (p.Ala414=)
c.24C>T (p.Ala8=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332260G>CCA491152637HCN4c.1242C>G (p.Ala414=)
c.24C>G (p.Ala8=)
15g.73332260G=CA2187169870HCN4c.1242C= (p.Ala414=)
c.24C= (p.Ala8=)
15g.73332260G>TCA491152636HCN4c.1242C>A (p.Ala414=)
c.24C>A (p.Ala8=)
15g.73332261G>ACA393094523HCN4c.1241C>T (p.Ala414Val)
c.23C>T (p.Ala8Val)
15g.73332261G>CCA16043944HCN4c.1241C>G (p.Ala414Gly)
c.23C>G (p.Ala8Gly)
ClinVar dbSNP
15g.73332261G=CA2187169874HCN4c.1241C= (p.Ala414=)
c.23C= (p.Ala8=)
15g.73332261G>TCA393094524HCN4c.1241C>A (p.Ala414Asp)
c.23C>A (p.Ala8Asp)
15g.73332262C>ACA393094525HCN4c.1240G>T (p.Ala414Ser)
c.22G>T (p.Ala8Ser)
15g.73332262C=CA2187169879HCN4c.1240G= (p.Ala414=)
c.22G= (p.Ala8=)
15g.73332262C>GCA393094526HCN4c.1240G>C (p.Ala414Pro)
c.22G>C (p.Ala8Pro)
15g.73332262C>TCA7649340HCN4c.1240G>A (p.Ala414Thr)
c.22G>A (p.Ala8Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73332263G>ACA7649341HCN4c.1239C>T (p.Ser413=)
c.21C>T (p.Ser7=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332263G>CCA393094527HCN4c.1239C>G (p.Ser413Arg)
c.21C>G (p.Ser7Arg)
15g.73332263G=CA2187169882HCN4c.1239C= (p.Ser413=)
c.21C= (p.Ser7=)
15g.73332263G>TCA393094528HCN4c.1239C>A (p.Ser413Arg)
c.21C>A (p.Ser7Arg)
15g.73332264C>ACA393094529HCN4c.1238G>T (p.Ser413Ile)
c.20G>T (p.Ser7Ile)
15g.73332264C>GCA393094530HCN4c.1238G>C (p.Ser413Thr)
c.20G>C (p.Ser7Thr)
15g.73332264C>TCA393094531HCN4c.1238G>A (p.Ser413Asn)
c.20G>A (p.Ser7Asn)
15g.73332265T>ACA393094534HCN4c.1237A>T (p.Ser413Cys)
c.19A>T (p.Ser7Cys)
15g.73332265T>CCA393094533HCN4c.1237A>G (p.Ser413Gly)
c.19A>G (p.Ser7Gly)
ClinVar dbSNP
15g.73332265T>GCA393094532HCN4c.1237A>C (p.Ser413Arg)
c.19A>C (p.Ser7Arg)
15g.73332265T=CA2187169885HCN4c.1237A= (p.Ser413=)
c.19A= (p.Ser7=)
15g.73332266G>ACA491152643HCN4c.1236C>T (p.Ala412=)
c.18C>T (p.Ala6=)
15g.73332266G>CCA491152644HCN4c.1236C>G (p.Ala412=)
c.18C>G (p.Ala6=)
15g.73332266G>TCA491152645HCN4c.1236C>A (p.Ala412=)
c.18C>A (p.Ala6=)
15g.73332267G>ACA393094535HCN4c.1235C>T (p.Ala412Val)
c.17C>T (p.Ala6Val)
15g.73332267G>CCA393094536HCN4c.1235C>G (p.Ala412Gly)
c.17C>G (p.Ala6Gly)
COSMIC
15g.73332267G>TCA393094537HCN4c.1235C>A (p.Ala412Asp)
c.17C>A (p.Ala6Asp)
15g.73332268C>ACA393094538HCN4c.1234G>T (p.Ala412Ser)
c.16G>T (p.Ala6Ser)
15g.73332268C>GCA393094539HCN4c.1234G>C (p.Ala412Pro)
c.16G>C (p.Ala6Pro)
15g.73332268C>TCA393094540HCN4c.1234G>A (p.Ala412Thr)
c.16G>A (p.Ala6Thr)
15g.73332269C>ACA491152649HCN4c.1233G>T (p.Leu411=)
c.15G>T (p.Leu5=)
15g.73332269C>GCA491152650HCN4c.1233G>C (p.Leu411=)
c.15G>C (p.Leu5=)
gnomAD v4
15g.73332269C>TCA491152651HCN4c.1233G>A (p.Leu411=)
c.15G>A (p.Leu5=)
gnomAD v4
15g.73332270A>CCA393094541HCN4c.1232T>G (p.Leu411Arg)
c.14T>G (p.Leu5Arg)
15g.73332270A>GCA393094543HCN4c.1232T>C (p.Leu411Pro)
c.14T>C (p.Leu5Pro)
15g.73332270A>TCA393094542HCN4c.1232T>A (p.Leu411Gln)
c.14T>A (p.Leu5Gln)
15g.73332271G>ACA491152655HCN4c.1231C>T (p.Leu411=)
c.13C>T (p.Leu5=)
15g.73332271G>CCA393094544HCN4c.1231C>G (p.Leu411Val)
c.13C>G (p.Leu5Val)
ClinVar gnomAD v4
15g.73332271G=CA2187169888HCN4c.1231C= (p.Leu411=)
c.13C= (p.Leu5=)
15g.73332271G>TCA393094545HCN4c.1231C>A (p.Leu411Met)
c.13C>A (p.Leu5Met)
dbSNP gnomAD v2
15g.73332272G>ACA491152656HCN4c.1230C>T (p.Asp410=)
c.12C>T (p.Asp4=)
15g.73332272G>CCA393094546HCN4c.1230C>G (p.Asp410Glu)
c.12C>G (p.Asp4Glu)
15g.73332272G>TCA393094547HCN4c.1230C>A (p.Asp410Glu)
c.12C>A (p.Asp4Glu)
15g.73332273T>ACA393094548HCN4c.1229A>T (p.Asp410Val)
c.11A>T (p.Asp4Val)
15g.73332273T>CCA393094549HCN4c.1229A>G (p.Asp410Gly)
c.11A>G (p.Asp4Gly)
15g.73332273T>GCA393094550HCN4c.1229A>C (p.Asp410Ala)
c.11A>C (p.Asp4Ala)
15g.73332274C>ACA393094551HCN4c.1228G>T (p.Asp410Tyr)
c.10G>T (p.Asp4Tyr)
gnomAD v4 COSMIC
15g.73332274C>GCA393094552HCN4c.1228G>C (p.Asp410His)
c.10G>C (p.Asp4His)
15g.73332274C>TCA393094553HCN4c.1228G>A (p.Asp410Asn)
c.10G>A (p.Asp4Asn)
COSMIC
15g.73332275G>ACA7649342HCN4c.1227C>T (p.Tyr409=)
c.9C>T (p.Tyr3=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73332275G>CCA393094555HCN4c.1227C>G (p.Tyr409Ter)
c.9C>G (p.Tyr3Ter)
15g.73332275G=CA2187169893HCN4c.1227C= (p.Tyr409=)
c.9C= (p.Tyr3=)
15g.73332275G>TCA393094554HCN4c.1227C>A (p.Tyr409Ter)
c.9C>A (p.Tyr3Ter)
15g.73332276T>ACA393094556HCN4c.1226A>T (p.Tyr409Phe)
c.8A>T (p.Tyr3Phe)
15g.73332276T>CCA393094557HCN4c.1226A>G (p.Tyr409Cys)
c.8A>G (p.Tyr3Cys)
15g.73332276T>GCA393094558HCN4c.1226A>C (p.Tyr409Ser)
c.8A>C (p.Tyr3Ser)

Number of alleles fetched