| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.51029595T>G | CA1909414679 | PRKG1 | c.266+37951T>G (n.266+37951T>G) | dbSNP |
| 10 | g.51029595T>C | CA207062103 | PRKG1 | c.266+37951T>C (n.266+37951T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.51029595T>A | CA1909414678 | PRKG1 | c.266+37951T>A (n.266+37951T>A) | dbSNP |