| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.30941459C>G | CA16621096 | MORC2 | c.798G>C (p.Arg266Ser) n.640G>C c.612G>C (p.Arg204Ser) n.352G>C c.822G>C (p.Arg274Ser) c.813G>C (p.Arg271Ser) c.663G>C (p.Arg221Ser) | ClinVar dbSNP |
| 22 | g.30941459C>A | CA411241151 | MORC2 | c.798G>T (p.Arg266Ser) n.640G>T c.612G>T (p.Arg204Ser) n.352G>T c.822G>T (p.Arg274Ser) c.813G>T (p.Arg271Ser) c.663G>T (p.Arg221Ser) | ClinVar dbSNP |