Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.67165841C>T | CA118625 | HSF4 | n.638C>T n.854C>T c.355C>T (p.Arg119Cys) c.229C>T (p.Arg77Cys) c.3C>T c.*102C>T (n.*102C>T) n.422C>T n.574C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.67165841C= | CA2229209017 | HSF4 | n.638C= n.854C= c.355C= (p.Arg119=) c.229C= (p.Arg77=) c.3C= c.*102C= (n.*102C=) n.422C= n.574C= | dbSNP |