| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.47587120T>C | CA2427975727 | SYN1 | c.775-9619A>G (n.775-9619A>G) | dbSNP |
| X | g.47587120T>G | CA329046241 | SYN1 | c.775-9619A>C (n.775-9619A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.47587120T= | CA2427975726 | SYN1 | c.775-9619A= (n.775-9619A=) | dbSNP |