| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.162281498C>T | CA163488 | IFIH1 | c.*951G>A (n.*951G>A) c.1354G>A (p.Ala452Thr) n.964G>A c.1042G>A (p.Ala348Thr) c.637G>A (p.Ala213Thr) | ClinVar dbSNP |
| 2 | g.162281498C= | CA1303148773 | IFIH1 | c.*951G= (n.*951G=) c.1354G= (p.Ala452=) n.964G= c.1042G= (p.Ala348=) c.637G= (p.Ala213=) | dbSNP |