Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|

17 | g.43047705T>A | CA003573 | BRCA1 | c.5407-2A>T (p.=) c.5266-2A>T (p.=) c.2095-2A>T (p.=) c.2021-2A>T (p.=) c.5470-2A>T (p.=) n.5543-2A>T n.5584-2A>T c.1981-2A>T (p.=) c.*5190-2A>T (p.=) c.337-2A>T (p.=) c.880-2A>T (p.=) c.106-2A>T (p.=) | ClinVar dbSNP |

17 | g.43047705T>C | CA003572 | BRCA1 | c.5407-2A>G (p.=) c.5266-2A>G (p.=) c.2095-2A>G (p.=) c.2021-2A>G (p.=) c.5470-2A>G (p.=) n.5543-2A>G n.5584-2A>G c.1981-2A>G (p.=) c.*5190-2A>G (p.=) c.337-2A>G (p.=) c.880-2A>G (p.=) c.106-2A>G (p.=) | ClinVar dbSNP |