Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.26779036T>GCA339183958ARID1Ac.5138T>G (p.Leu1713Arg)
c.3989T>G (p.Leu1330Arg)
c.3986T>G (p.Leu1329Arg)
c.555T>G
c.3992T>G (p.Leu1331Arg)
n.938T>G
c.1827T>G
c.4487T>G (p.Leu1496Arg)
c.636T>G
dbSNP
1g.26779036T>ACA339183957ARID1Ac.5138T>A (p.Leu1713Gln)
c.3989T>A (p.Leu1330Gln)
c.3986T>A (p.Leu1329Gln)
c.555T>A
c.3992T>A (p.Leu1331Gln)
n.938T>A
c.1827T>A
c.4487T>A (p.Leu1496Gln)
c.636T>A
dbSNP COSMIC
1g.26779036T>CCA208601ARID1Ac.5138T>C (p.Leu1713Pro)
c.3989T>C (p.Leu1330Pro)
c.3986T>C (p.Leu1329Pro)
c.555T>C
c.3992T>C (p.Leu1331Pro)
n.938T>C
c.1827T>C
c.4487T>C (p.Leu1496Pro)
c.636T>C
ClinVar dbSNP COSMIC

Number of alleles fetched