Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129533710C>T | CA256663 | RHO | c.1039C>T (p.Pro347Ser) | ClinVar dbSNP |
3 | g.129533710C>A | CA354471278 | RHO | c.1039C>A (p.Pro347Thr) | ClinVar dbSNP |
3 | g.129533710C>G | CA354471279 | RHO | c.1039C>G (p.Pro347Ala) | ClinVar dbSNP |
3 | g.129533710C= | CA1401213449 | RHO | c.1039C= (p.Pro347=) | dbSNP |