| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.10142124G>A | CA020230 | VHL | c.277G>A (p.Gly93Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 3 | g.10142124G>C | CA357130 | VHL | c.277G>C (p.Gly93Arg) | ClinVar dbSNP COSMIC |
| 3 | g.10142124G>T | CA357106 | VHL | c.277G>T (p.Gly93Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.10142124G= | CA1345066132 | VHL | c.277G= (p.Gly93=) | dbSNP |