Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.119278238G>C | CA382912659 | CBL | c.*620G>C (n.*620G>C) c.1168G>C (p.Asp390His) c.1162G>C (p.Asp388His) | ClinVar dbSNP |
11 | g.119278238G>T | CA123488 | CBL | c.*620G>T (n.*620G>T) c.1168G>T (p.Asp390Tyr) c.1162G>T (p.Asp388Tyr) | ClinVar dbSNP |
11 | g.119278238G>A | CA382912657 | CBL | c.*620G>A (n.*620G>A) c.1168G>A (p.Asp390Asn) c.1162G>A (p.Asp388Asn) | dbSNP |