A35V (p.Ala35Val) variant of CD28 (P10747)
A35V (p.Ala35Val) in CD28 (P10747) 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 0.19 / 1. The record also includes population frequency data and structural context.
A35V (p.Ala35Val) variant details
- p.Ala35Val
- rs1202305808
- NCI-TCGA Cosmic COSV1001
- cosmic curated COSV10014
- NCI-TCGA Cosmic COSV9904
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.186
- REVEL 0.13
- MetaLR 0.18
- MetaSVM -0.84
- CADD 1.83
- PolyPhen-2 0.12
- SIFT 0.26
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available