| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.10142110G>T | CA351750675 | VHL | c.263G>T (p.Trp88Leu) | dbSNP COSMIC |
| 3 | g.10142110G>A | CA020197 | VHL | c.263G>A (p.Trp88Ter) | ClinVar dbSNP COSMIC |
| 3 | g.10142110G>C | CA020202 | VHL | c.263G>C (p.Trp88Ser) | ClinVar dbSNP COSMIC |
| 3 | g.10142110G= | CA1345066056 | VHL | c.263G= (p.Trp88=) | dbSNP |