Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.12022931_12022933dup | CA69951917 | SYN2 | c.377+18003_377+18005dup (n.377+18003_377+18005dup) n.563+18003_563+18005dup | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.12022931_12022933del | CA2701931307 | SYN2 | c.377+18003_377+18005del (n.377+18003_377+18005del) n.563+18003_563+18005del | dbSNP |