| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| Y | g.8599012G>C | CA1139016943 | c.89+5983C>G (n.89+5983C>G) c.93-20389C>G (n.93-20389C>G) | dbSNP gnomAD v3 gnomAD v4 | |
| Y | g.8599012G>A | CA337623057 | c.89+5983C>T (n.89+5983C>T) c.93-20389C>T (n.93-20389C>T) | dbSNP gnomAD v3 gnomAD v4 |