G94A (p.Gly94Ala) variant of COMP (P49747)
G94A (p.Gly94Ala) in COMP (P49747) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G94A (p.Gly94Ala) variant details
- p.Gly94Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available