Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.119278256T>C | CA128668 | CBL | c.*638T>C (n.*638T>C) c.1186T>C (p.Cys396Arg) c.1180T>C (p.Cys394Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
11 | g.119278256T>A | CA382912715 | CBL | c.*638T>A (n.*638T>A) c.1186T>A (p.Cys396Ser) c.1180T>A (p.Cys394Ser) | dbSNP gnomAD v4 |
11 | g.119278256T>G | CA382912721 | CBL | c.*638T>G (n.*638T>G) c.1186T>G (p.Cys396Gly) c.1180T>G (p.Cys394Gly) | dbSNP gnomAD v4 COSMIC |
11 | g.119278256T= | CA2003905990 | CBL | c.*638T= (n.*638T=) c.1186T= (p.Cys396=) c.1180T= (p.Cys394=) | dbSNP |