Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.97584820C>T | CA471091106 | HOGA1 | c.117C>T (p.Tyr39=) n.498C>T | ClinVar dbSNP gnomAD v4 |
10 | g.97584820C>A | CA203942 | HOGA1 | c.117C>A (p.Tyr39Ter) n.498C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.97584820C= | CA1930492629 | HOGA1 | c.117C= (p.Tyr39=) n.498C= | dbSNP |