| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.97854657C>A | CA374348384 | FOXE1 | c.743C>A (p.Ala248Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.97854657C>G | CA204453 | FOXE1 | c.743C>G (p.Ala248Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.97854657C>T | CA374348385 | FOXE1 | c.743C>T (p.Ala248Val) | dbSNP gnomAD v4 |