Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7567421A>T | CA362675719 | DSP | c.1112A>T (p.His371Leu) n.436A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.7567421A>G | CA362675718 | DSP | c.1112A>G (p.His371Arg) n.436A>G | ClinVar dbSNP |
6 | g.7567421A>C | CA004777 | DSP | c.1112A>C (p.His371Pro) n.436A>C | ClinVar dbSNP gnomAD v4 |
6 | g.7567421A= | CA1608620719 | DSP | c.1112A= (p.His371=) n.436A= | dbSNP |