Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.10142179G>T | CA357019 | VHL | c.332G>T (p.Ser111Ile) | ClinVar dbSNP COSMIC |
3 | g.10142179G>C | CA351751328 | VHL | c.332G>C (p.Ser111Thr) | dbSNP |
3 | g.10142179G>A | CA357091 | VHL | c.332G>A (p.Ser111Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.10142179G= | CA1345066522 | VHL | c.332G= (p.Ser111=) | dbSNP |