| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100598284C>T | CA333839948 | TNMD | c.577+627C>T (n.577+627C>T) c.388+627C>T (n.388+627C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.100598284C>A | CA2448039608 | TNMD | c.577+627C>A (n.577+627C>A) c.388+627C>A (n.388+627C>A) | dbSNP |
| X | g.100598284C>G | CA2448039609 | TNMD | c.577+627C>G (n.577+627C>G) c.388+627C>G (n.388+627C>G) | dbSNP |