Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7565469C>A | CA362674520 | DSP | c.888C>A (p.Tyr296Ter) n.212C>A n.406C>A | ClinVar dbSNP |
6 | g.7565469C>T | CA052938 | DSP | c.888C>T (p.Tyr296=) n.212C>T n.406C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.7565469C>G | CA007801 | DSP | c.888C>G (p.Tyr296Ter) n.212C>G n.406C>G | ClinVar dbSNP |