G32D (p.Gly32Asp) variant of MCCC2 (Q9HCC0)
G32D (p.Gly32Asp) in MCCC2 (Q9HCC0) 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 0.59 / 1. The record also includes population frequency data and structural context.
G32D (p.Gly32Asp) variant details
- p.Gly32Asp
- NCI-TCGA Cosmic COSV6015
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.587
- REVEL 0.57
- CADD 22.50
- PolyPhen-2 0.01
- SIFT 0.17
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available