Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.26779863C>A | CA416968970 | ARID1A | c.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 |
1 | g.26779863C>T | CA10576101 | ARID1A | c.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 |
1 | g.26779863C>G | CA339189201 | ARID1A | c.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 |