Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32337431A>T | CA017194 | BRCA2 | c.3076A>T (p.Lys1026Ter) c.2707A>T (p.Lys903Ter) n.3076A>T | ClinVar dbSNP gnomAD v4 |
13 | g.32337431A>G | CA387775191 | BRCA2 | c.3076A>G (p.Lys1026Glu) c.2707A>G (p.Lys903Glu) n.3076A>G | dbSNP gnomAD v4 |
13 | g.32337431A= | CA2082814208 | BRCA2 | c.3076A= (p.Lys1026=) c.2707A= (p.Lys903=) n.3076A= | dbSNP |