Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
6g.149379115C>TCA452720660TAB2n.1615C>T
c.1200C>T (p.Val400=)
c.348C>T (p.Val116=)
c.1104C>T (p.Val368=)
6g.149379116A=CA1671916043TAB2n.1616A=
c.1201A= (p.Met401=)
c.349A= (p.Met117=)
c.1105A= (p.Met369=)
6g.149379116A>CCA365998172TAB2n.1616A>C
c.1201A>C (p.Met401Leu)
c.349A>C (p.Met117Leu)
c.1105A>C (p.Met369Leu)
6g.149379116A>GCA365998174TAB2n.1616A>G
c.1201A>G (p.Met401Val)
c.349A>G (p.Met117Val)
c.1105A>G (p.Met369Val)
 dbSNP gnomAD v4
6g.149379116A>TCA365998173TAB2n.1616A>T
c.1201A>T (p.Met401Leu)
c.349A>T (p.Met117Leu)
c.1105A>T (p.Met369Leu)
6g.149379117T>ACA365998175TAB2n.1617T>A
c.1202T>A (p.Met401Lys)
c.350T>A (p.Met117Lys)
c.1106T>A (p.Met369Lys)
6g.149379117T>CCA365998176TAB2n.1617T>C
c.1202T>C (p.Met401Thr)
c.350T>C (p.Met117Thr)
c.1106T>C (p.Met369Thr)
 dbSNP
6g.149379117T>GCA365998177TAB2n.1617T>G
c.1202T>G (p.Met401Arg)
c.350T>G (p.Met117Arg)
c.1106T>G (p.Met369Arg)
6g.149379117T=CA1671916046TAB2n.1617T=
c.1202T= (p.Met401=)
c.350T= (p.Met117=)
c.1106T= (p.Met369=)
6g.149379118G>ACA365998178TAB2n.1618G>A
c.1203G>A (p.Met401Ile)
c.351G>A (p.Met117Ile)
c.1107G>A (p.Met369Ile)
 gnomAD v4
6g.149379118G>CCA365998179TAB2n.1618G>C
c.1203G>C (p.Met401Ile)
c.351G>C (p.Met117Ile)
c.1107G>C (p.Met369Ile)
6g.149379118G>TCA365998180TAB2n.1618G>T
c.1203G>T (p.Met401Ile)
c.351G>T (p.Met117Ile)
c.1107G>T (p.Met369Ile)
6g.149379119C>ACA452720675TAB2n.1619C>A
c.1204C>A (p.Arg402=)
c.352C>A (p.Arg118=)
c.1108C>A (p.Arg370=)
6g.149379119C=CA1671916048TAB2n.1619C=
c.1204C= (p.Arg402=)
c.352C= (p.Arg118=)
c.1108C= (p.Arg370=)
6g.149379119C>GCA365998181TAB2n.1619C>G
c.1204C>G (p.Arg402Gly)
c.352C>G (p.Arg118Gly)
c.1108C>G (p.Arg370Gly)
6g.149379119C>TCA4041509TAB2n.1619C>T
c.1204C>T (p.Arg402Trp)
c.352C>T (p.Arg118Trp)
c.1108C>T (p.Arg370Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.149379120G>ACA365998182TAB2n.1620G>A
c.1205G>A (p.Arg402Gln)
c.353G>A (p.Arg118Gln)
c.1109G>A (p.Arg370Gln)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
6g.149379120G>CCA365998183TAB2n.1620G>C
c.1205G>C (p.Arg402Pro)
c.353G>C (p.Arg118Pro)
c.1109G>C (p.Arg370Pro)
6g.149379120G=CA1671916052TAB2n.1620G=
c.1205G= (p.Arg402=)
c.353G= (p.Arg118=)
c.1109G= (p.Arg370=)
6g.149379120G>TCA365998184TAB2n.1620G>T
c.1205G>T (p.Arg402Leu)
c.353G>T (p.Arg118Leu)
c.1109G>T (p.Arg370Leu)
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)

Number of alleles fetched