| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.56385014C>A | CA23054262 | c.759+93872G>T (n.759+93872G>T) c.366+15080G>T c.192+98249G>T c.378+98249G>T c.768+98249G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 1 | g.56385014C>T | CA737156480 | c.759+93872G>A (n.759+93872G>A) c.366+15080G>A c.192+98249G>A c.378+98249G>A c.768+98249G>A | dbSNP gnomAD v3 gnomAD v4 |