Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.26779863C>ACA416968970ARID1Ac.5965C>A (p.Arg1989=)
c.4816C>A (p.Arg1606=)
c.4813C>A (p.Arg1605=)
c.1382C>A
c.4819C>A (p.Arg1607=)
n.1765C>A
c.2654C>A
c.5314C>A (p.Arg1772=)
c.1463C>A
dbSNP gnomAD v4
1g.26779863C>TCA10576101ARID1Ac.5965C>T (p.Arg1989Ter)
c.4816C>T (p.Arg1606Ter)
c.4813C>T (p.Arg1605Ter)
c.1382C>T
c.4819C>T (p.Arg1607Ter)
n.1765C>T
c.2654C>T
c.5314C>T (p.Arg1772Ter)
c.1463C>T
ClinVar dbSNP COSMIC
1g.26779863C>GCA339189201ARID1Ac.5965C>G (p.Arg1989Gly)
c.4816C>G (p.Arg1606Gly)
c.4813C>G (p.Arg1605Gly)
c.1382C>G
c.4819C>G (p.Arg1607Gly)
n.1765C>G
c.2654C>G
c.5314C>G (p.Arg1772Gly)
c.1463C>G
ClinVar dbSNP

Number of alleles fetched