| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.5302226C>T | CA259603 | PROKR2 | c.969G>A (p.Met323Ile) c.861G>A (p.Met287Ile) | ClinVar dbSNP |
| 20 | g.5302226C= | CA2347436313 | PROKR2 | c.969G= (p.Met323=) c.861G= (p.Met287=) | dbSNP |
| 20 | g.5302226C>A | CA408166557 | PROKR2 | c.969G>T (p.Met323Ile) c.861G>T (p.Met287Ile) | dbSNP gnomAD v4 |