Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129528884G>C | CA256687 | RHO | c.151G>C (p.Gly51Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.129528884G>T | CA354495943 | RHO | c.151G>T (p.Gly51Cys) | dbSNP |
3 | g.129528884G= | CA1401205449 | RHO | c.151G= (p.Gly51=) | dbSNP |