Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.10142184C>T | CA348491 | VHL | c.337C>T (p.Arg113Ter) | ClinVar dbSNP COSMIC |
3 | g.10142184C>A | CA040327 | VHL | c.337C>A (p.Arg113=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.10142184C>G | CA351751365 | VHL | c.337C>G (p.Arg113Gly) | ClinVar dbSNP gnomAD v4 |
3 | g.10142184C= | CA1345066550 | VHL | c.337C= (p.Arg113=) | dbSNP |