Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.38682852T>A | CA364348231 | GLO1 | c.332A>T (p.Glu111Val) n.364A>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.38682852T>G | CA126152 | GLO1 | c.332A>C (p.Glu111Ala) n.364A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.38682852T= | CA1622355676 | GLO1 | c.332A= (p.Glu111=) n.364A= | dbSNP |