| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.5313911C>T | CA10603471 | PROKR2 | c.458+1G>A (n.458+1G>A) c.350+1G>A (n.350+1G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.5313911C= | CA2347441579 | PROKR2 | c.458+1G= (n.458+1G=) c.350+1G= (n.350+1G=) | dbSNP |