| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.10142116A>C | CA351750709 | VHL | c.269A>C (p.Asn90Thr) | ClinVar dbSNP |
| 3 | g.10142116A>G | CA020212 | VHL | c.269A>G (p.Asn90Ser) | ClinVar dbSNP gnomAD v4 |
| 3 | g.10142116A>T | CA357043 | VHL | c.269A>T (p.Asn90Ile) | ClinVar dbSNP COSMIC |
| 3 | g.10142116A= | CA1345066090 | VHL | c.269A= (p.Asn90=) | dbSNP |