Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.97584820C>TCA471091106HOGA1c.117C>T (p.Tyr39=)
n.498C>T
ClinVar dbSNP gnomAD v4
10g.97584820C>ACA203942HOGA1c.117C>A (p.Tyr39Ter)
n.498C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched