Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157196221C>GCA366238246ARID1Bc.4129C>G (p.Gln1377Glu)
c.4198C>G (p.Gln1400Glu)
c.4417C>G (p.Gln1473Glu)
c.4168C>G (p.Gln1390Glu)
c.3880C>G (p.Gln1294Glu)
c.2446C>G (p.Gln816Glu)
c.1609C>G (p.Gln537Glu)
c.1240C>G (p.Gln414Glu)
n.2751C>G
c.4288C>G (p.Gln1430Glu)
n.2285C>G
c.1656C>G
c.1570C>G
n.954C>G
c.1630C>G (p.Gln544Glu)
c.1789C>G (p.Gln597Glu)
c.3919C>G (p.Gln1307Glu)
c.4039C>G (p.Gln1347Glu)
c.3118C>G (p.Gln1040Glu)
c.2938C>G (p.Gln980Glu)
c.2698C>G (p.Gln900Glu)
c.2317C>G (p.Gln773Glu)
c.1180C>G (p.Gln394Glu)
c.4249C>G (p.Gln1417Glu)
c.4150C>G (p.Gln1384Glu)
c.4120C>G (p.Gln1374Glu)
c.4090C>G (p.Gln1364Glu)
c.3961C>G (p.Gln1321Glu)
c.3940C>G (p.Gln1314Glu)
n.4332C>G
dbSNP
6g.157196221C>ACA366238244ARID1Bc.4129C>A (p.Gln1377Lys)
c.4198C>A (p.Gln1400Lys)
c.4417C>A (p.Gln1473Lys)
c.4168C>A (p.Gln1390Lys)
c.3880C>A (p.Gln1294Lys)
c.2446C>A (p.Gln816Lys)
c.1609C>A (p.Gln537Lys)
c.1240C>A (p.Gln414Lys)
n.2751C>A
c.4288C>A (p.Gln1430Lys)
n.2285C>A
c.1656C>A
c.1570C>A
n.954C>A
c.1630C>A (p.Gln544Lys)
c.1789C>A (p.Gln597Lys)
c.3919C>A (p.Gln1307Lys)
c.4039C>A (p.Gln1347Lys)
c.3118C>A (p.Gln1040Lys)
c.2938C>A (p.Gln980Lys)
c.2698C>A (p.Gln900Lys)
c.2317C>A (p.Gln773Lys)
c.1180C>A (p.Gln394Lys)
c.4249C>A (p.Gln1417Lys)
c.4150C>A (p.Gln1384Lys)
c.4120C>A (p.Gln1374Lys)
c.4090C>A (p.Gln1364Lys)
c.3961C>A (p.Gln1321Lys)
c.3940C>A (p.Gln1314Lys)
n.4332C>A
dbSNP
6g.157196221C>TCA129762ARID1Bc.4129C>T (p.Gln1377Ter)
c.4198C>T (p.Gln1400Ter)
c.4417C>T (p.Gln1473Ter)
c.4168C>T (p.Gln1390Ter)
c.3880C>T (p.Gln1294Ter)
c.2446C>T (p.Gln816Ter)
c.1609C>T (p.Gln537Ter)
c.1240C>T (p.Gln414Ter)
n.2751C>T
c.4288C>T (p.Gln1430Ter)
n.2285C>T
c.1656C>T
c.1570C>T
n.954C>T
c.1630C>T (p.Gln544Ter)
c.1789C>T (p.Gln597Ter)
c.3919C>T (p.Gln1307Ter)
c.4039C>T (p.Gln1347Ter)
c.3118C>T (p.Gln1040Ter)
c.2938C>T (p.Gln980Ter)
c.2698C>T (p.Gln900Ter)
c.2317C>T (p.Gln773Ter)
c.1180C>T (p.Gln394Ter)
c.4249C>T (p.Gln1417Ter)
c.4150C>T (p.Gln1384Ter)
c.4120C>T (p.Gln1374Ter)
c.4090C>T (p.Gln1364Ter)
c.3961C>T (p.Gln1321Ter)
c.3940C>T (p.Gln1314Ter)
n.4332C>T
ClinVar dbSNP gnomAD v4 COSMIC COSMIC

Number of alleles fetched