Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.97601889G>T | CA5634231 | HOGA1 | c.733G>T (p.Val245Phe) c.143G>T c.244G>T (p.Val82Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.97601889G>A | CA203959 | HOGA1 | c.733G>A (p.Val245Ile) c.143G>A c.244G>A (p.Val82Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |