G22A (p.Gly22Ala) variant of COMP (P49747)
G22A (p.Gly22Ala) in COMP (P49747) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes structural context.
G22A (p.Gly22Ala) variant details
- p.Gly22Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.27
- ESM-1b 0.00
- AlphaMissense 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available