| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154604995G>T | CA108774409 | FGG | c.1201C>A (p.Arg401=) c.1225C>A (p.Arg409=) n.749C>A n.1743C>A | dbSNP |
| 4 | g.154604995G>A | CA108774405 | FGG | c.1201C>T (p.Arg401Trp) c.1225C>T (p.Arg409Trp) n.749C>T n.1743C>T | ClinVar dbSNP gnomAD v4 |
| 4 | g.154604995G>C | CA126410 | FGG | c.1201C>G (p.Arg401Gly) c.1225C>G (p.Arg409Gly) n.749C>G n.1743C>G | ClinVar dbSNP |