Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129529049G>T | CA256669 | RHO | c.316G>T (p.Gly106Trp) | ClinVar dbSNP |
3 | g.129529049G>C | CA354496864 | RHO | c.316G>C (p.Gly106Arg) | ClinVar dbSNP |
3 | g.129529049G>A | CA256683 | RHO | c.316G>A (p.Gly106Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129529049G= | CA1401206060 | RHO | c.316G= (p.Gly106=) | dbSNP |