Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.12045605_12045609dup | CA69988973 | SYN2 | c.377+40677_377+40681dup (n.377+40677_377+40681dup) n.563+40677_563+40681dup | dbSNP |
3 | g.12045605_12045609del | CA69988975 | SYN2 | c.377+40677_377+40681del (n.377+40677_377+40681del) n.563+40677_563+40681del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |