Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.25390874C>A | CA339067260 | RHCE | c.676G>T (p.Ala226Ser) c.487-1761G>T (n.487-1761G>T) c.487-5030G>T (n.487-5030G>T) c.628G>T (p.Ala210Ser) n.831G>T c.107+11722G>T c.*132-1761G>T (n.*132-1761G>T) c.556G>T (p.Ala186Ser) c.547G>T (p.Ala183Ser) c.508G>T (p.Ala170Ser) c.781G>T (p.Ala261Ser) c.-4294966581G>T | dbSNP |
1 | g.25390874C>T | CA339067261 | RHCE | c.676G>A (p.Ala226Thr) c.487-1761G>A (n.487-1761G>A) c.487-5030G>A (n.487-5030G>A) c.628G>A (p.Ala210Thr) n.831G>A c.107+11722G>A c.*132-1761G>A (n.*132-1761G>A) c.556G>A (p.Ala186Thr) c.547G>A (p.Ala183Thr) c.508G>A (p.Ala170Thr) c.781G>A (p.Ala261Thr) c.-4294966581G>A | dbSNP |
1 | g.25390874C>G | CA694712 | RHCE | c.676G>C (p.Ala226Pro) c.487-1761G>C (n.487-1761G>C) c.487-5030G>C (n.487-5030G>C) c.628G>C (p.Ala210Pro) n.831G>C c.107+11722G>C c.*132-1761G>C (n.*132-1761G>C) c.556G>C (p.Ala186Pro) c.547G>C (p.Ala183Pro) c.508G>C (p.Ala170Pro) c.781G>C (p.Ala261Pro) c.-4294966581G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |