| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.45370684G>T | CA633349785 | ERCC2 | c.-519C>A (n.-519C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.45370684G>C | CA14677027 | ERCC2 | c.-519C>G (n.-519C>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.45370684G>A | CA2338399046 | ERCC2 | c.-519C>T (n.-519C>T) | dbSNP gnomAD v4 |