Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.149379101G>ACA4041507TAB2n.1601G>A
c.1186G>A (p.Gly396Arg)
c.334G>A (p.Gly112Arg)
c.1090G>A (p.Gly364Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.149379101G>CCA365998138TAB2n.1601G>C
c.1186G>C (p.Gly396Arg)
c.334G>C (p.Gly112Arg)
c.1090G>C (p.Gly364Arg)
6g.149379101G=CA1671916020TAB2n.1601G=
c.1186G= (p.Gly396=)
c.334G= (p.Gly112=)
c.1090G= (p.Gly364=)
6g.149379101G>TCA365998139TAB2n.1601G>T
c.1186G>T (p.Gly396Ter)
c.334G>T (p.Gly112Ter)
c.1090G>T (p.Gly364Ter)
6g.149379102G>ACA365998140TAB2n.1602G>A
c.1187G>A (p.Gly396Glu)
c.335G>A (p.Gly112Glu)
c.1091G>A (p.Gly364Glu)
6g.149379102G>CCA365998141TAB2n.1602G>C
c.1187G>C (p.Gly396Ala)
c.335G>C (p.Gly112Ala)
c.1091G>C (p.Gly364Ala)
 COSMIC
6g.149379102G>TCA365998142TAB2n.1602G>T
c.1187G>T (p.Gly396Val)
c.335G>T (p.Gly112Val)
c.1091G>T (p.Gly364Val)
6g.149379103A>CCA452720602TAB2n.1603A>C
c.1188A>C (p.Gly396=)
c.336A>C (p.Gly112=)
c.1092A>C (p.Gly364=)
6g.149379103A>GCA452720605TAB2n.1603A>G
c.1188A>G (p.Gly396=)
c.336A>G (p.Gly112=)
c.1092A>G (p.Gly364=)
6g.149379103A>TCA452720608TAB2n.1603A>T
c.1188A>T (p.Gly396=)
c.336A>T (p.Gly112=)
c.1092A>T (p.Gly364=)
6g.149379104G>ACA365998143TAB2n.1604G>A
c.1189G>A (p.Asp397Asn)
c.337G>A (p.Asp113Asn)
c.1093G>A (p.Asp365Asn)
6g.149379104G>CCA365998145TAB2n.1604G>C
c.1189G>C (p.Asp397His)
c.337G>C (p.Asp113His)
c.1093G>C (p.Asp365His)
6g.149379104G>TCA365998144TAB2n.1604G>T
c.1189G>T (p.Asp397Tyr)
c.337G>T (p.Asp113Tyr)
c.1093G>T (p.Asp365Tyr)
6g.149379105A>CCA365998146TAB2n.1605A>C
c.1190A>C (p.Asp397Ala)
c.338A>C (p.Asp113Ala)
c.1094A>C (p.Asp365Ala)
6g.149379105A>GCA365998147TAB2n.1605A>G
c.1190A>G (p.Asp397Gly)
c.338A>G (p.Asp113Gly)
c.1094A>G (p.Asp365Gly)
6g.149379105A>TCA365998148TAB2n.1605A>T
c.1190A>T (p.Asp397Val)
c.338A>T (p.Asp113Val)
c.1094A>T (p.Asp365Val)
6g.149379106T>ACA365998149TAB2n.1606T>A
c.1191T>A (p.Asp397Glu)
c.339T>A (p.Asp113Glu)
c.1095T>A (p.Asp365Glu)
6g.149379106T>CCA452720624TAB2n.1606T>C
c.1191T>C (p.Asp397=)
c.339T>C (p.Asp113=)
c.1095T>C (p.Asp365=)
 gnomAD v4
6g.149379106T>GCA365998150TAB2n.1606T>G
c.1191T>G (p.Asp397Glu)
c.339T>G (p.Asp113Glu)
c.1095T>G (p.Asp365Glu)
6g.149379107G>ACA365998151TAB2n.1607G>A
c.1192G>A (p.Glu398Lys)
c.340G>A (p.Glu114Lys)
c.1096G>A (p.Glu366Lys)
 dbSNP gnomAD v4
6g.149379107G>CCA365998152TAB2n.1607G>C
c.1192G>C (p.Glu398Gln)
c.340G>C (p.Glu114Gln)
c.1096G>C (p.Glu366Gln)
6g.149379107G=CA1671916023TAB2n.1607G=
c.1192G= (p.Glu398=)
c.340G= (p.Glu114=)
c.1096G= (p.Glu366=)
6g.149379107G>TCA365998153TAB2n.1607G>T
c.1192G>T (p.Glu398Ter)
c.340G>T (p.Glu114Ter)
c.1096G>T (p.Glu366Ter)
6g.149379108A>CCA365998154TAB2n.1608A>C
c.1193A>C (p.Glu398Ala)
c.341A>C (p.Glu114Ala)
c.1097A>C (p.Glu366Ala)
6g.149379108A>GCA365998155TAB2n.1608A>G
c.1193A>G (p.Glu398Gly)
c.341A>G (p.Glu114Gly)
c.1097A>G (p.Glu366Gly)
6g.149379108A>TCA365998156TAB2n.1608A>T
c.1193A>T (p.Glu398Val)
c.341A>T (p.Glu114Val)
c.1097A>T (p.Glu366Val)
6g.149379109A>CCA365998158TAB2n.1609A>C
c.1194A>C (p.Glu398Asp)
c.342A>C (p.Glu114Asp)
c.1098A>C (p.Glu366Asp)
6g.149379109A>GCA452720637TAB2n.1609A>G
c.1194A>G (p.Glu398=)
c.342A>G (p.Glu114=)
c.1098A>G (p.Glu366=)
 gnomAD v4
6g.149379109A>TCA365998157TAB2n.1609A>T
c.1194A>T (p.Glu398Asp)
c.342A>T (p.Glu114Asp)
c.1098A>T (p.Glu366Asp)
6g.149379110C>ACA365998159TAB2n.1610C>A
c.1195C>A (p.Gln399Lys)
c.343C>A (p.Gln115Lys)
c.1099C>A (p.Gln367Lys)
6g.149379110C=CA1671916027TAB2n.1610C=
c.1195C= (p.Gln399=)
c.343C= (p.Gln115=)
c.1099C= (p.Gln367=)
6g.149379110C>GCA365998160TAB2n.1610C>G
c.1195C>G (p.Gln399Glu)
c.343C>G (p.Gln115Glu)
c.1099C>G (p.Gln367Glu)
6g.149379110C>TCA16042638TAB2n.1610C>T
c.1195C>T (p.Gln399Ter)
c.343C>T (p.Gln115Ter)
c.1099C>T (p.Gln367Ter)
 ClinVar dbSNP
6g.149379111A>CCA365998161TAB2n.1611A>C
c.1196A>C (p.Gln399Pro)
c.344A>C (p.Gln115Pro)
c.1100A>C (p.Gln367Pro)
6g.149379111A>GCA365998162TAB2n.1611A>G
c.1196A>G (p.Gln399Arg)
c.344A>G (p.Gln115Arg)
c.1100A>G (p.Gln367Arg)
6g.149379111A>TCA365998163TAB2n.1611A>T
c.1196A>T (p.Gln399Leu)
c.344A>T (p.Gln115Leu)
c.1100A>T (p.Gln367Leu)
6g.149379112G>ACA4041508TAB2n.1612G>A
c.1197G>A (p.Gln399=)
c.345G>A (p.Gln115=)
c.1101G>A (p.Gln367=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.149379112G>CCA365998165TAB2n.1612G>C
c.1197G>C (p.Gln399His)
c.345G>C (p.Gln115His)
c.1101G>C (p.Gln367His)
6g.149379112G=CA1671916030TAB2n.1612G=
c.1197G= (p.Gln399=)
c.345G= (p.Gln115=)
c.1101G= (p.Gln367=)
6g.149379112G>TCA365998164TAB2n.1612G>T
c.1197G>T (p.Gln399His)
c.345G>T (p.Gln115His)
c.1101G>T (p.Gln367His)
6g.149379113G>ACA365998166TAB2n.1613G>A
c.1198G>A (p.Val400Ile)
c.346G>A (p.Val116Ile)
c.1102G>A (p.Val368Ile)
 gnomAD v4
6g.149379113G>CCA365998167TAB2n.1613G>C
c.1198G>C (p.Val400Leu)
c.346G>C (p.Val116Leu)
c.1102G>C (p.Val368Leu)
6g.149379113G>TCA365998168TAB2n.1613G>T
c.1198G>T (p.Val400Phe)
c.346G>T (p.Val116Phe)
c.1102G>T (p.Val368Phe)
6g.149379114T>ACA365998169TAB2n.1614T>A
c.1199T>A (p.Val400Asp)
c.347T>A (p.Val116Asp)
c.1103T>A (p.Val368Asp)
 dbSNP
6g.149379114T>CCA365998170TAB2n.1614T>C
c.1199T>C (p.Val400Ala)
c.347T>C (p.Val116Ala)
c.1103T>C (p.Val368Ala)
 dbSNP gnomAD v3 gnomAD v4
6g.149379114T>GCA365998171TAB2n.1614T>G
c.1199T>G (p.Val400Gly)
c.347T>G (p.Val116Gly)
c.1103T>G (p.Val368Gly)
6g.149379114T=CA1671916035TAB2n.1614T=
c.1199T= (p.Val400=)
c.347T= (p.Val116=)
c.1103T= (p.Val368=)
6g.149379115C>ACA452720664TAB2n.1615C>A
c.1200C>A (p.Val400=)
c.348C>A (p.Val116=)
c.1104C>A (p.Val368=)
6g.149379115C=CA1671916039TAB2n.1615C=
c.1200C= (p.Val400=)
c.348C= (p.Val116=)
c.1104C= (p.Val368=)
6g.149379115C>GCA452720661TAB2n.1615C>G
c.1200C>G (p.Val400=)
c.348C>G (p.Val116=)
c.1104C>G (p.Val368=)
 dbSNP

Number of alleles fetched