Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32355114C>T | CA025004 | BRCA2 | c.7261C>T (p.Gln2421Ter) c.6892C>T (p.Gln2298Ter) n.7261C>T c.7165C>T (p.Gln2389Ter) | ClinVar dbSNP |
13 | g.32355114C>A | CA387740550 | BRCA2 | c.7261C>A (p.Gln2421Lys) c.6892C>A (p.Gln2298Lys) n.7261C>A c.7165C>A (p.Gln2389Lys) | dbSNP |
13 | g.32355114C>G | CA387740552 | BRCA2 | c.7261C>G (p.Gln2421Glu) c.6892C>G (p.Gln2298Glu) n.7261C>G c.7165C>G (p.Gln2389Glu) | dbSNP |