Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.10300722G>A | CA14769299 | SNAP25 | c.552+1310G>A (n.552+1310G>A) n.2780+1310G>A n.966+1310G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.10300722G= | CA2349731132 | SNAP25 | c.552+1310G= (n.552+1310G=) n.2780+1310G= n.966+1310G= | dbSNP |