E49G (p.Glu49Gly) variant of CNGA1 (P29973)
E49G (p.Glu49Gly) 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.
E49G (p.Glu49Gly) variant details
- p.Glu49Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available