Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32363370A>T | CA025485 | BRCA2 | c.8168A>T (p.Asp2723Val) c.7799A>T (p.Asp2600Val) c.635A>T (p.Asp212Val) c.8176A>T (n.8176A>T) c.733A>T c.8072A>T (p.Asp2691Val) | ClinVar dbSNP gnomAD v4 |
13 | g.32363370A>G | CA025484 | BRCA2 | c.8168A>G (p.Asp2723Gly) c.7799A>G (p.Asp2600Gly) c.635A>G (p.Asp212Gly) c.8176A>G (n.8176A>G) c.733A>G c.8072A>G (p.Asp2691Gly) | ClinVar dbSNP gnomAD v4 |
13 | g.32363370A>C | CA025483 | BRCA2 | c.8168A>C (p.Asp2723Ala) c.7799A>C (p.Asp2600Ala) c.635A>C (p.Asp212Ala) c.8176A>C (n.8176A>C) c.733A>C c.8072A>C (p.Asp2691Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |