Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32340314C>T | CA023417 | BRCA2 | c.5959C>T (p.Gln1987Ter) c.5590C>T (p.Gln1864Ter) n.5959C>T | ClinVar dbSNP COSMIC COSMIC |
13 | g.32340314C>G | CA387787606 | BRCA2 | c.5959C>G (p.Gln1987Glu) c.5590C>G (p.Gln1864Glu) n.5959C>G | dbSNP COSMIC COSMIC |
13 | g.32340314C>A | CA387787605 | BRCA2 | c.5959C>A (p.Gln1987Lys) c.5590C>A (p.Gln1864Lys) n.5959C>A | dbSNP |