Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.149379201G>ACA365998514TAB2n.1701G>A
c.1286G>A (p.Gly429Asp)
c.434G>A (p.Gly145Asp)
c.1190G>A (p.Gly397Asp)
6g.149379201G>CCA365998516TAB2n.1701G>C
c.1286G>C (p.Gly429Ala)
c.434G>C (p.Gly145Ala)
c.1190G>C (p.Gly397Ala)
6g.149379201G>TCA365998518TAB2n.1701G>T
c.1286G>T (p.Gly429Val)
c.434G>T (p.Gly145Val)
c.1190G>T (p.Gly397Val)
6g.149379202T>ACA452720989TAB2n.1702T>A
c.1287T>A (p.Gly429=)
c.435T>A (p.Gly145=)
c.1191T>A (p.Gly397=)
6g.149379202T>CCA452720992TAB2n.1702T>C
c.1287T>C (p.Gly429=)
c.435T>C (p.Gly145=)
c.1191T>C (p.Gly397=)
6g.149379202T>GCA452720993TAB2n.1702T>G
c.1287T>G (p.Gly429=)
c.435T>G (p.Gly145=)
c.1191T>G (p.Gly397=)
6g.149379203C>ACA365998522TAB2n.1703C>A
c.1288C>A (p.Pro430Thr)
c.436C>A (p.Pro146Thr)
c.1192C>A (p.Pro398Thr)
6g.149379203C>GCA365998524TAB2n.1703C>G
c.1288C>G (p.Pro430Ala)
c.436C>G (p.Pro146Ala)
c.1192C>G (p.Pro398Ala)
6g.149379203C>TCA365998526TAB2n.1703C>T
c.1288C>T (p.Pro430Ser)
c.436C>T (p.Pro146Ser)
c.1192C>T (p.Pro398Ser)
6g.149379204C>ACA365998530TAB2n.1704C>A
c.1289C>A (p.Pro430His)
c.437C>A (p.Pro146His)
c.1193C>A (p.Pro398His)
6g.149379204C>GCA365998532TAB2n.1704C>G
c.1289C>G (p.Pro430Arg)
c.437C>G (p.Pro146Arg)
c.1193C>G (p.Pro398Arg)
6g.149379204C>TCA365998534TAB2n.1704C>T
c.1289C>T (p.Pro430Leu)
c.437C>T (p.Pro146Leu)
c.1193C>T (p.Pro398Leu)
 gnomAD v4
6g.149379205T>ACA452720998TAB2n.1705T>A
c.1290T>A (p.Pro430=)
c.438T>A (p.Pro146=)
c.1194T>A (p.Pro398=)
6g.149379205T>CCA452720999TAB2n.1705T>C
c.1290T>C (p.Pro430=)
c.438T>C (p.Pro146=)
c.1194T>C (p.Pro398=)
6g.149379205T>GCA452721000TAB2n.1705T>G
c.1290T>G (p.Pro430=)
c.438T>G (p.Pro146=)
c.1194T>G (p.Pro398=)
 gnomAD v4
6g.149379206G>ACA365998537TAB2n.1706G>A
c.1291G>A (p.Ala431Thr)
c.439G>A (p.Ala147Thr)
c.1195G>A (p.Ala399Thr)
6g.149379206G>CCA365998540TAB2n.1706G>C
c.1291G>C (p.Ala431Pro)
c.439G>C (p.Ala147Pro)
c.1195G>C (p.Ala399Pro)
6g.149379206G>TCA365998542TAB2n.1706G>T
c.1291G>T (p.Ala431Ser)
c.439G>T (p.Ala147Ser)
c.1195G>T (p.Ala399Ser)
6g.149379207C>ACA365998546TAB2n.1707C>A
c.1292C>A (p.Ala431Asp)
c.440C>A (p.Ala147Asp)
c.1196C>A (p.Ala399Asp)
6g.149379207C>GCA365998550TAB2n.1707C>G
c.1292C>G (p.Ala431Gly)
c.440C>G (p.Ala147Gly)
c.1196C>G (p.Ala399Gly)
6g.149379207C>TCA365998548TAB2n.1707C>T
c.1292C>T (p.Ala431Val)
c.440C>T (p.Ala147Val)
c.1196C>T (p.Ala399Val)
6g.149379208C>ACA452721008TAB2n.1708C>A
c.1293C>A (p.Ala431=)
c.441C>A (p.Ala147=)
c.1197C>A (p.Ala399=)
6g.149379208C=CA1671916139TAB2n.1708C=
c.1293C= (p.Ala431=)
c.441C= (p.Ala147=)
c.1197C= (p.Ala399=)
6g.149379208C>GCA452721010TAB2n.1708C>G
c.1293C>G (p.Ala431=)
c.441C>G (p.Ala147=)
c.1197C>G (p.Ala399=)
 gnomAD v4
6g.149379208C>TCA452721011TAB2n.1708C>T
c.1293C>T (p.Ala431=)
c.441C>T (p.Ala147=)
c.1197C>T (p.Ala399=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.149379209T>ACA365998553TAB2n.1709T>A
c.1294T>A (p.Phe432Ile)
c.442T>A (p.Phe148Ile)
c.1198T>A (p.Phe400Ile)
6g.149379209T>CCA365998557TAB2n.1709T>C
c.1294T>C (p.Phe432Leu)
c.442T>C (p.Phe148Leu)
c.1198T>C (p.Phe400Leu)
 gnomAD v4
6g.149379209T>GCA365998555TAB2n.1709T>G
c.1294T>G (p.Phe432Val)
c.442T>G (p.Phe148Val)
c.1198T>G (p.Phe400Val)
6g.149379210T>ACA365998560TAB2n.1710T>A
c.1295T>A (p.Phe432Tyr)
c.443T>A (p.Phe148Tyr)
c.1199T>A (p.Phe400Tyr)
6g.149379210T>CCA365998562TAB2n.1710T>C
c.1295T>C (p.Phe432Ser)
c.443T>C (p.Phe148Ser)
c.1199T>C (p.Phe400Ser)
6g.149379210T>GCA365998564TAB2n.1710T>G
c.1295T>G (p.Phe432Cys)
c.443T>G (p.Phe148Cys)
c.1199T>G (p.Phe400Cys)
6g.149379211T>ACA365998566TAB2n.1711T>A
c.1296T>A (p.Phe432Leu)
c.444T>A (p.Phe148Leu)
c.1200T>A (p.Phe400Leu)
6g.149379211T>CCA452721014TAB2n.1711T>C
c.1296T>C (p.Phe432=)
c.444T>C (p.Phe148=)
c.1200T>C (p.Phe400=)
 gnomAD v4
6g.149379211T>GCA365998568TAB2n.1711T>G
c.1296T>G (p.Phe432Leu)
c.444T>G (p.Phe148Leu)
c.1200T>G (p.Phe400Leu)
6g.149379212A>CCA365998571TAB2n.1712A>C
c.1297A>C (p.Ile433Leu)
c.445A>C (p.Ile149Leu)
c.1201A>C (p.Ile401Leu)
6g.149379212A>GCA365998573TAB2n.1712A>G
c.1297A>G (p.Ile433Val)
c.445A>G (p.Ile149Val)
c.1201A>G (p.Ile401Val)
6g.149379212A>TCA365998574TAB2n.1712A>T
c.1297A>T (p.Ile433Phe)
c.445A>T (p.Ile149Phe)
c.1201A>T (p.Ile401Phe)
6g.149379213T>ACA365998576TAB2n.1713T>A
c.1298T>A (p.Ile433Asn)
c.446T>A (p.Ile149Asn)
c.1202T>A (p.Ile401Asn)
6g.149379213T>CCA365998578TAB2n.1713T>C
c.1298T>C (p.Ile433Thr)
c.446T>C (p.Ile149Thr)
c.1202T>C (p.Ile401Thr)
 dbSNP gnomAD v2 gnomAD v4
6g.149379213T>GCA365998580TAB2n.1713T>G
c.1298T>G (p.Ile433Ser)
c.446T>G (p.Ile149Ser)
c.1202T>G (p.Ile401Ser)
6g.149379213T=CA1671916142TAB2n.1713T=
c.1298T= (p.Ile433=)
c.446T= (p.Ile149=)
c.1202T= (p.Ile401=)
6g.149379214T>ACA452721025TAB2n.1714T>A
c.1299T>A (p.Ile433=)
c.447T>A (p.Ile149=)
c.1203T>A (p.Ile401=)
6g.149379214T>CCA452721024TAB2n.1714T>C
c.1299T>C (p.Ile433=)
c.447T>C (p.Ile149=)
c.1203T>C (p.Ile401=)
6g.149379214T>GCA365998582TAB2n.1714T>G
c.1299T>G (p.Ile433Met)
c.447T>G (p.Ile149Met)
c.1203T>G (p.Ile401Met)
6g.149379215C>ACA365998585TAB2n.1715C>A
c.1300C>A (p.His434Asn)
c.448C>A (p.His150Asn)
c.1204C>A (p.His402Asn)
6g.149379215C>GCA365998583TAB2n.1715C>G
c.1300C>G (p.His434Asp)
c.448C>G (p.His150Asp)
c.1204C>G (p.His402Asp)
6g.149379215C>TCA365998584TAB2n.1715C>T
c.1300C>T (p.His434Tyr)
c.448C>T (p.His150Tyr)
c.1204C>T (p.His402Tyr)
6g.149379216A>CCA365998588TAB2n.1716A>C
c.1301A>C (p.His434Pro)
c.449A>C (p.His150Pro)
c.1205A>C (p.His402Pro)
6g.149379216A>GCA365998590TAB2n.1716A>G
c.1301A>G (p.His434Arg)
c.449A>G (p.His150Arg)
c.1205A>G (p.His402Arg)
 gnomAD v4
6g.149379216A>TCA365998592TAB2n.1716A>T
c.1301A>T (p.His434Leu)
c.449A>T (p.His150Leu)
c.1205A>T (p.His402Leu)

Number of alleles fetched