| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.102846899G>C | CA114363 | PAH | c.965C>G (p.Ala322Gly) c.950C>G (p.Ala317Gly) n.724C>G n.627C>G c.74-2468C>G n.480C>G c.913-2468C>G (n.913-2468C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.102846899G>A | CA16020905 | PAH | c.965C>T (p.Ala322Val) c.950C>T (p.Ala317Val) n.724C>T n.627C>T c.74-2468C>T n.480C>T c.913-2468C>T (n.913-2468C>T) | dbSNP gnomAD v4 COSMIC |