A87D (p.Ala87Asp) variant of CHM (P24386)
A87D (p.Ala87Asp) in CHM (P24386) 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 0.11 / 1. The record also includes population frequency data and structural context.
A87D (p.Ala87Asp) variant details
- p.Ala87Asp
- NCI-TCGA Cosmic COSV6256
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.112
- REVEL 0.03
- MetaLR 0.11
- MetaSVM -1.03
- CADD 13.40
- PolyPhen-2 0.06
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available