Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.149379121G>ACA452720682TAB2n.1621G>A
c.1206G>A (p.Arg402=)
c.354G>A (p.Arg118=)
c.1110G>A (p.Arg370=)
6g.149379121G>CCA452720689TAB2n.1621G>C
c.1206G>C (p.Arg402=)
c.354G>C (p.Arg118=)
c.1110G>C (p.Arg370=)
COSMIC
6g.149379121G>TCA452720692TAB2n.1621G>T
c.1206G>T (p.Arg402=)
c.354G>T (p.Arg118=)
c.1110G>T (p.Arg370=)
6g.149379122A>CCA365998185TAB2n.1622A>C
c.1207A>C (p.Asn403His)
c.355A>C (p.Asn119His)
c.1111A>C (p.Asn371His)
6g.149379122A>GCA365998187TAB2n.1622A>G
c.1207A>G (p.Asn403Asp)
c.355A>G (p.Asn119Asp)
c.1111A>G (p.Asn371Asp)
6g.149379122A>TCA365998186TAB2n.1622A>T
c.1207A>T (p.Asn403Tyr)
c.355A>T (p.Asn119Tyr)
c.1111A>T (p.Asn371Tyr)
6g.149379123A=CA1671916056TAB2n.1623A=
c.1208A= (p.Asn403=)
c.356A= (p.Asn119=)
c.1112A= (p.Asn371=)
6g.149379123A>CCA365998188TAB2n.1623A>C
c.1208A>C (p.Asn403Thr)
c.356A>C (p.Asn119Thr)
c.1112A>C (p.Asn371Thr)
6g.149379123A>GCA4041510TAB2n.1623A>G
c.1208A>G (p.Asn403Ser)
c.356A>G (p.Asn119Ser)
c.1112A>G (p.Asn371Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.149379123A>TCA365998189TAB2n.1623A>T
c.1208A>T (p.Asn403Ile)
c.356A>T (p.Asn119Ile)
c.1112A>T (p.Asn371Ile)
6g.149379124T>ACA365998190TAB2n.1624T>A
c.1209T>A (p.Asn403Lys)
c.357T>A (p.Asn119Lys)
c.1113T>A (p.Asn371Lys)
6g.149379124T>CCA452720701TAB2n.1624T>C
c.1209T>C (p.Asn403=)
c.357T>C (p.Asn119=)
c.1113T>C (p.Asn371=)
6g.149379124T>GCA365998191TAB2n.1624T>G
c.1209T>G (p.Asn403Lys)
c.357T>G (p.Asn119Lys)
c.1113T>G (p.Asn371Lys)
6g.149379125C>ACA365998192TAB2n.1625C>A
c.1210C>A (p.Gln404Lys)
c.358C>A (p.Gln120Lys)
c.1114C>A (p.Gln372Lys)
6g.149379125C>GCA365998194TAB2n.1625C>G
c.1210C>G (p.Gln404Glu)
c.358C>G (p.Gln120Glu)
c.1114C>G (p.Gln372Glu)
gnomAD v4
6g.149379125C>TCA365998193TAB2n.1625C>T
c.1210C>T (p.Gln404Ter)
c.358C>T (p.Gln120Ter)
c.1114C>T (p.Gln372Ter)
6g.149379126A>CCA365998195TAB2n.1626A>C
c.1211A>C (p.Gln404Pro)
c.359A>C (p.Gln120Pro)
c.1115A>C (p.Gln372Pro)
6g.149379126A>GCA365998196TAB2n.1626A>G
c.1211A>G (p.Gln404Arg)
c.359A>G (p.Gln120Arg)
c.1115A>G (p.Gln372Arg)
6g.149379126A>TCA365998197TAB2n.1626A>T
c.1211A>T (p.Gln404Leu)
c.359A>T (p.Gln120Leu)
c.1115A>T (p.Gln372Leu)
gnomAD v4
6g.149379127G>ACA452720713TAB2n.1627G>A
c.1212G>A (p.Gln404=)
c.360G>A (p.Gln120=)
c.1116G>A (p.Gln372=)
gnomAD v4
6g.149379127G>CCA365998198TAB2n.1627G>C
c.1212G>C (p.Gln404His)
c.360G>C (p.Gln120His)
c.1116G>C (p.Gln372His)
6g.149379127G>TCA365998199TAB2n.1627G>T
c.1212G>T (p.Gln404His)
c.360G>T (p.Gln120His)
c.1116G>T (p.Gln372His)
6g.149379128C>ACA365998200TAB2n.1628C>A
c.1213C>A (p.Pro405Thr)
c.361C>A (p.Pro121Thr)
c.1117C>A (p.Pro373Thr)
6g.149379128C>GCA365998201TAB2n.1628C>G
c.1213C>G (p.Pro405Ala)
c.361C>G (p.Pro121Ala)
c.1117C>G (p.Pro373Ala)
6g.149379128C>TCA365998202TAB2n.1628C>T
c.1213C>T (p.Pro405Ser)
c.361C>T (p.Pro121Ser)
c.1117C>T (p.Pro373Ser)
6g.149379129C>ACA365998203TAB2n.1629C>A
c.1214C>A (p.Pro405His)
c.362C>A (p.Pro121His)
c.1118C>A (p.Pro373His)
6g.149379129C>GCA365998204TAB2n.1629C>G
c.1214C>G (p.Pro405Arg)
c.362C>G (p.Pro121Arg)
c.1118C>G (p.Pro373Arg)
6g.149379129C>TCA365998205TAB2n.1629C>T
c.1214C>T (p.Pro405Leu)
c.362C>T (p.Pro121Leu)
c.1118C>T (p.Pro373Leu)
6g.149379130C>ACA452720723TAB2n.1630C>A
c.1215C>A (p.Pro405=)
c.363C>A (p.Pro121=)
c.1119C>A (p.Pro373=)
6g.149379130C>GCA452720724TAB2n.1630C>G
c.1215C>G (p.Pro405=)
c.363C>G (p.Pro121=)
c.1119C>G (p.Pro373=)
6g.149379130C>TCA452720726TAB2n.1630C>T
c.1215C>T (p.Pro405=)
c.363C>T (p.Pro121=)
c.1119C>T (p.Pro373=)
gnomAD v4
6g.149379131A>CCA365998208TAB2n.1631A>C
c.1216A>C (p.Thr406Pro)
c.364A>C (p.Thr122Pro)
c.1120A>C (p.Thr374Pro)
6g.149379131A>GCA365998207TAB2n.1631A>G
c.1216A>G (p.Thr406Ala)
c.364A>G (p.Thr122Ala)
c.1120A>G (p.Thr374Ala)
gnomAD v4 COSMIC
6g.149379131A>TCA365998206TAB2n.1631A>T
c.1216A>T (p.Thr406Ser)
c.364A>T (p.Thr122Ser)
c.1120A>T (p.Thr374Ser)
6g.149379132C>ACA365998209TAB2n.1632C>A
c.1217C>A (p.Thr406Lys)
c.365C>A (p.Thr122Lys)
c.1121C>A (p.Thr374Lys)
6g.149379132C>GCA365998210TAB2n.1632C>G
c.1217C>G (p.Thr406Arg)
c.365C>G (p.Thr122Arg)
c.1121C>G (p.Thr374Arg)
6g.149379132C>TCA365998211TAB2n.1632C>T
c.1217C>T (p.Thr406Ile)
c.365C>T (p.Thr122Ile)
c.1121C>T (p.Thr374Ile)
6g.149379133A=CA1671916061TAB2n.1633A=
c.1218A= (p.Thr406=)
c.366A= (p.Thr122=)
c.1122A= (p.Thr374=)
6g.149379133A>CCA149917397TAB2n.1633A>C
c.1218A>C (p.Thr406=)
c.366A>C (p.Thr122=)
c.1122A>C (p.Thr374=)
dbSNP gnomAD v4
6g.149379133A>GCA452720741TAB2n.1633A>G
c.1218A>G (p.Thr406=)
c.366A>G (p.Thr122=)
c.1122A>G (p.Thr374=)
dbSNP gnomAD v4 COSMIC
6g.149379133A>TCA4041511TAB2n.1633A>T
c.1218A>T (p.Thr406=)
c.366A>T (p.Thr122=)
c.1122A>T (p.Thr374=)
dbSNP ExAC gnomAD v2
6g.149379134C>ACA365998212TAB2n.1634C>A
c.1219C>A (p.Leu407Ile)
c.367C>A (p.Leu123Ile)
c.1123C>A (p.Leu375Ile)
6g.149379134C=CA1671916065TAB2n.1634C=
c.1219C= (p.Leu407=)
c.367C= (p.Leu123=)
c.1123C= (p.Leu375=)
6g.149379134C>GCA365998213TAB2n.1634C>G
c.1219C>G (p.Leu407Val)
c.367C>G (p.Leu123Val)
c.1123C>G (p.Leu375Val)
6g.149379134C>TCA365998214TAB2n.1634C>T
c.1219C>T (p.Leu407Phe)
c.367C>T (p.Leu123Phe)
c.1123C>T (p.Leu375Phe)
dbSNP
6g.149379135T>ACA365998215TAB2n.1635T>A
c.1220T>A (p.Leu407His)
c.368T>A (p.Leu123His)
c.1124T>A (p.Leu375His)
6g.149379135T>CCA365998216TAB2n.1635T>C
c.1220T>C (p.Leu407Pro)
c.368T>C (p.Leu123Pro)
c.1124T>C (p.Leu375Pro)
6g.149379135T>GCA365998217TAB2n.1635T>G
c.1220T>G (p.Leu407Arg)
c.368T>G (p.Leu123Arg)
c.1124T>G (p.Leu375Arg)
6g.149379136C>ACA452720750TAB2n.1636C>A
c.1221C>A (p.Leu407=)
c.369C>A (p.Leu123=)
c.1125C>A (p.Leu375=)
6g.149379136C=CA1671916067TAB2n.1636C=
c.1221C= (p.Leu407=)
c.369C= (p.Leu123=)
c.1125C= (p.Leu375=)

Number of alleles fetched