Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.24277772A>T | CA1616427655 | DCDC2 | c.922+277T>A (n.922+277T>A) | dbSNP |
6 | g.24277772A>G | CA136634427 | DCDC2 | c.922+277T>C (n.922+277T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.24277772A>C | CA1616427653 | DCDC2 | c.922+277T>G (n.922+277T>G) | dbSNP |