Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32336892C>A | CA387772497 | BRCA2 | c.2537C>A (p.Ser846Ter) c.2168C>A (p.Ser723Ter) n.2537C>A | dbSNP |
13 | g.32336892C>T | CA387772498 | BRCA2 | c.2537C>T (p.Ser846Leu) c.2168C>T (p.Ser723Leu) n.2537C>T | ClinVar dbSNP |
13 | g.32336892C>G | CA015578 | BRCA2 | c.2537C>G (p.Ser846Ter) c.2168C>G (p.Ser723Ter) n.2537C>G | ClinVar dbSNP |