Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
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

Number of alleles fetched