| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.7572029A>C | CA448525567 | DSP | c.2091A>C (p.Gly697=) n.732A>C | dbSNP |
| 6 | g.7572029A>G | CA005242 | DSP | c.2091A>G (p.Gly697=) n.732A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.7572029A>T | CA448525570 | DSP | c.2091A>T (p.Gly697=) n.732A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |