| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.894156C>T | CA4961650 | DMRT1 | c.783C>T (p.Pro261=) n.932C>T c.309C>T (p.Pro103=) c.831C>T (p.Pro277=) c.587-22607C>T (n.587-22607C>T) c.539-22607C>T (n.539-22607C>T) c.237C>T (p.Pro79=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.894156C>G | CA4961651 | DMRT1 | c.783C>G (p.Pro261=) n.932C>G c.309C>G (p.Pro103=) c.831C>G (p.Pro277=) c.587-22607C>G (n.587-22607C>G) c.539-22607C>G (n.539-22607C>G) c.237C>G (p.Pro79=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.894156C= | CA1827190881 | DMRT1 | c.783C= (p.Pro261=) n.932C= c.309C= (p.Pro103=) c.831C= (p.Pro277=) c.587-22607C= (n.587-22607C=) c.539-22607C= (n.539-22607C=) c.237C= (p.Pro79=) | dbSNP |