E107Q (p.Glu107Gln) variant of CNGA1 (P29973)
E107Q (p.Glu107Gln) in CNGA1 (P29973) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E107Q (p.Glu107Gln) variant details
- p.Glu107Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available