| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32355250T>C | CA157623 | BRCA2 | c.7397T>C (p.Val2466Ala) c.7028T>C (p.Val2343Ala) n.7397T>C c.7301T>C (p.Val2434Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32355250T= | CA025053 | BRCA2 | c.7397T= (p.Val2466=) c.7028T= (p.Val2343=) n.7397T= c.7301T= (p.Val2434=) | ClinVar dbSNP |
| 13 | g.32355250T>G | CA387741814 | BRCA2 | c.7397T>G (p.Val2466Gly) c.7028T>G (p.Val2343Gly) n.7397T>G c.7301T>G (p.Val2434Gly) | dbSNP |