Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.133352509G>A | CA10603164 | SURF1 | c.688C>T (p.Arg230Ter) n.598C>T n.678C>T c.361C>T (p.Arg121Ter) | ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4 |
9 | g.133352509G= | CA1882634144 | SURF1 | c.688C= (p.Arg230=) n.598C= n.678C= c.361C= (p.Arg121=) | dbSNP |