G92V (p.Gly92Val) variant of TNFRSF4 (P43489)
G92V (p.Gly92Val) in TNFRSF4 (P43489) 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 0.80 / 1. The record also includes population frequency data.
G92V (p.Gly92Val) variant details
- p.Gly92Val
- NCI-TCGA Cosmic COSV5541
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.802
- REVEL 0.84
- CADD 23.90
- PolyPhen-2 0.97
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available