| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.192335434C>T | CA10588956 | FGF12 | c.341G>A (p.Arg114His) n.408G>A c.155G>A (p.Arg52His) n.343G>A n.374G>A c.83G>A (p.Arg28His) c.44G>A (p.Arg15His) c.233G>A (p.Arg78His) c.146G>A (p.Arg49His) | ClinVar dbSNP COSMIC COSMIC |
| 3 | g.192335434C>A | CA355866459 | FGF12 | c.341G>T (p.Arg114Leu) n.408G>T c.155G>T (p.Arg52Leu) n.343G>T n.374G>T c.83G>T (p.Arg28Leu) c.44G>T (p.Arg15Leu) c.233G>T (p.Arg78Leu) c.146G>T (p.Arg49Leu) | dbSNP |
| 3 | g.192335434C= | CA1429666100 | FGF12 | c.341G= (p.Arg114=) n.408G= c.155G= (p.Arg52=) n.343G= n.374G= c.83G= (p.Arg28=) c.44G= (p.Arg15=) c.233G= (p.Arg78=) c.146G= (p.Arg49=) | dbSNP |