Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32362691C>G | CA025361 | BRCA2 | c.7974C>G (p.Tyr2658Ter) c.7605C>G (p.Tyr2535Ter) c.441C>G (p.Tyr147Ter) c.7982C>G (n.7982C>G) c.539C>G c.7878C>G (p.Tyr2626Ter) | ClinVar dbSNP |
13 | g.32362691C>T | CA483261063 | BRCA2 | c.7974C>T (p.Tyr2658=) c.7605C>T (p.Tyr2535=) c.441C>T (p.Tyr147=) c.7982C>T (n.7982C>T) c.539C>T c.7878C>T (p.Tyr2626=) | ClinVar dbSNP |
13 | g.32362691C>A | CA10589460 | BRCA2 | c.7974C>A (p.Tyr2658Ter) c.7605C>A (p.Tyr2535Ter) c.441C>A (p.Tyr147Ter) c.7982C>A (n.7982C>A) c.539C>A c.7878C>A (p.Tyr2626Ter) | ClinVar dbSNP |