| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.72195460G>A | CA16042767 | FOLR1 | c.357+1G>A (n.357+1G>A) | ClinVar dbSNP |
| 11 | g.72195460G= | CA1981879973 | FOLR1 | c.357+1G= (n.357+1G=) | dbSNP |
| 11 | g.72195460G>C | CA381732825 | FOLR1 | c.357+1G>C (n.357+1G>C) | dbSNP gnomAD v4 |