Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157198899C>TCA151059ARID1Bc.4312C>T (p.Gln1438Ter)
c.4381C>T (p.Gln1461Ter)
c.4600C>T (p.Gln1534Ter)
c.4351C>T (p.Gln1451Ter)
c.4063C>T (p.Gln1355Ter)
c.2629C>T (p.Gln877Ter)
c.1792C>T (p.Gln598Ter)
c.1423C>T (p.Gln475Ter)
n.2934C>T
n.391C>T
c.4471C>T (p.Gln1491Ter)
n.2468C>T
c.1839C>T
c.1753C>T
n.1137C>T
c.1813C>T (p.Gln605Ter)
c.1972C>T (p.Gln658Ter)
c.4102C>T (p.Gln1368Ter)
c.4222C>T (p.Gln1408Ter)
c.3301C>T (p.Gln1101Ter)
c.3121C>T (p.Gln1041Ter)
c.2881C>T (p.Gln961Ter)
c.2500C>T (p.Gln834Ter)
c.1363C>T (p.Gln455Ter)
c.4432C>T (p.Gln1478Ter)
c.4333C>T (p.Gln1445Ter)
c.4303C>T (p.Gln1435Ter)
c.4273C>T (p.Gln1425Ter)
c.4144C>T (p.Gln1382Ter)
c.4123C>T (p.Gln1375Ter)
n.4427-1806C>T
ClinVar dbSNP
6g.157198899C=CA1675542249ARID1Bc.4312C= (p.Gln1438=)
c.4381C= (p.Gln1461=)
c.4600C= (p.Gln1534=)
c.4351C= (p.Gln1451=)
c.4063C= (p.Gln1355=)
c.2629C= (p.Gln877=)
c.1792C= (p.Gln598=)
c.1423C= (p.Gln475=)
n.2934C=
n.391C=
c.4471C= (p.Gln1491=)
n.2468C=
c.1839C=
c.1753C=
n.1137C=
c.1813C= (p.Gln605=)
c.1972C= (p.Gln658=)
c.4102C= (p.Gln1368=)
c.4222C= (p.Gln1408=)
c.3301C= (p.Gln1101=)
c.3121C= (p.Gln1041=)
c.2881C= (p.Gln961=)
c.2500C= (p.Gln834=)
c.1363C= (p.Gln455=)
c.4432C= (p.Gln1478=)
c.4333C= (p.Gln1445=)
c.4303C= (p.Gln1435=)
c.4273C= (p.Gln1425=)
c.4144C= (p.Gln1382=)
c.4123C= (p.Gln1375=)
n.4427-1806C=
dbSNP

Number of alleles fetched