A36V (p.Ala36Val) variant of CDKN1A (P38936)
A36V (p.Ala36Val) in CDKN1A (P38936) 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 0.46 / 1. The record also includes population frequency data and structural context.
A36V (p.Ala36Val) variant details
- p.Ala36Val
- rs746709171
- NCI-TCGA Cosmic COSV9978
- cosmic curated COSV99781
- ExAC rs746709171
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.462
- AlphaMissense 0.18
- MetaLR 0.42
- MetaSVM -0.58
- PolyPhen-2 0.90
- SIFT 0.08
- MutPred 0.37
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available