| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.152648922C>T | CA4582330 | XRCC2 | c.395G>A (p.Arg132His) c.563G>A (p.Arg188His) n.585G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648922C>G | CA370198419 | XRCC2 | c.395G>C (p.Arg132Pro) c.563G>C (p.Arg188Pro) n.585G>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.152648922C>A | CA370198418 | XRCC2 | c.395G>T (p.Arg132Leu) c.563G>T (p.Arg188Leu) n.585G>T | ClinVar dbSNP gnomAD v4 |
| 7 | g.152648922C= | CA1753247102 | XRCC2 | c.395G= (p.Arg132=) c.563G= (p.Arg188=) n.585G= | dbSNP |