| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.47449163G>C | CA10587996 | RAPSN | c.-199C>G (n.-199C>G) | ClinVar dbSNP |
| 11 | g.47449163G>T | CA2613410744 | RAPSN | c.-199C>A (n.-199C>A) | dbSNP gnomAD v4 |
| 11 | g.47449163G= | CA1969379750 | RAPSN | c.-199C= (n.-199C=) | dbSNP |