Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129530917C>G | CA354498053 | RHO | c.403C>G (p.Arg135Gly) | ClinVar dbSNP |
3 | g.129530917C>T | CA122819 | RHO | c.403C>T (p.Arg135Trp) | ClinVar dbSNP gnomAD v4 |
3 | g.129530917C= | CA1401209282 | RHO | c.403C= (p.Arg135=) | dbSNP |
3 | g.129530917C>A | CA435643780 | RHO | c.403C>A (p.Arg135=) | dbSNP gnomAD v4 |