Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157181137C>TCA129764ARID1Bc.3514C>T (p.Arg1172Ter)
c.3583C>T (p.Arg1195Ter)
c.3802C>T (p.Arg1268Ter)
c.1687C>T (p.Arg563Ter)
c.3553C>T (p.Arg1185Ter)
c.3265C>T (p.Arg1089Ter)
c.1831C>T (p.Arg611Ter)
c.994C>T (p.Arg332Ter)
c.628C>T (p.Arg210Ter)
c.3673C>T (p.Arg1225Ter)
n.1670C>T
c.1041C>T
c.955C>T
n.339C>T
c.1015C>T (p.Arg339Ter)
c.1174C>T (p.Arg392Ter)
c.3304C>T (p.Arg1102Ter)
c.1690C>T (p.Arg564Ter)
c.466C>T (p.Arg156Ter)
c.875C>T
c.3424C>T (p.Arg1142Ter)
c.2503C>T (p.Arg835Ter)
c.2323C>T (p.Arg775Ter)
c.2083C>T (p.Arg695Ter)
c.1702C>T (p.Arg568Ter)
c.565C>T (p.Arg189Ter)
c.3634C>T (p.Arg1212Ter)
c.3535C>T (p.Arg1179Ter)
c.3505C>T (p.Arg1169Ter)
c.3475C>T (p.Arg1159Ter)
c.3346C>T (p.Arg1116Ter)
c.3325C>T (p.Arg1109Ter)
n.3717C>T
ClinVar dbSNP
6g.157181137C>ACA452780818ARID1Bc.3514C>A (p.Arg1172=)
c.3583C>A (p.Arg1195=)
c.3802C>A (p.Arg1268=)
c.1687C>A (p.Arg563=)
c.3553C>A (p.Arg1185=)
c.3265C>A (p.Arg1089=)
c.1831C>A (p.Arg611=)
c.994C>A (p.Arg332=)
c.628C>A (p.Arg210=)
c.3673C>A (p.Arg1225=)
n.1670C>A
c.1041C>A
c.955C>A
n.339C>A
c.1015C>A (p.Arg339=)
c.1174C>A (p.Arg392=)
c.3304C>A (p.Arg1102=)
c.1690C>A (p.Arg564=)
c.466C>A (p.Arg156=)
c.875C>A
c.3424C>A (p.Arg1142=)
c.2503C>A (p.Arg835=)
c.2323C>A (p.Arg775=)
c.2083C>A (p.Arg695=)
c.1702C>A (p.Arg568=)
c.565C>A (p.Arg189=)
c.3634C>A (p.Arg1212=)
c.3535C>A (p.Arg1179=)
c.3505C>A (p.Arg1169=)
c.3475C>A (p.Arg1159=)
c.3346C>A (p.Arg1116=)
c.3325C>A (p.Arg1109=)
n.3717C>A
dbSNP gnomAD v4
6g.157181137C>GCA366228259ARID1Bc.3514C>G (p.Arg1172Gly)
c.3583C>G (p.Arg1195Gly)
c.3802C>G (p.Arg1268Gly)
c.1687C>G (p.Arg563Gly)
c.3553C>G (p.Arg1185Gly)
c.3265C>G (p.Arg1089Gly)
c.1831C>G (p.Arg611Gly)
c.994C>G (p.Arg332Gly)
c.628C>G (p.Arg210Gly)
c.3673C>G (p.Arg1225Gly)
n.1670C>G
c.1041C>G
c.955C>G
n.339C>G
c.1015C>G (p.Arg339Gly)
c.1174C>G (p.Arg392Gly)
c.3304C>G (p.Arg1102Gly)
c.1690C>G (p.Arg564Gly)
c.466C>G (p.Arg156Gly)
c.875C>G
c.3424C>G (p.Arg1142Gly)
c.2503C>G (p.Arg835Gly)
c.2323C>G (p.Arg775Gly)
c.2083C>G (p.Arg695Gly)
c.1702C>G (p.Arg568Gly)
c.565C>G (p.Arg189Gly)
c.3634C>G (p.Arg1212Gly)
c.3535C>G (p.Arg1179Gly)
c.3505C>G (p.Arg1169Gly)
c.3475C>G (p.Arg1159Gly)
c.3346C>G (p.Arg1116Gly)
c.3325C>G (p.Arg1109Gly)
n.3717C>G
dbSNP

Number of alleles fetched