G13V (p.Gly13Val) variant of TNFRSF1B (P20333)
G13V (p.Gly13Val) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
G13V (p.Gly13Val) variant details
- p.Gly13Val
- gnomAD 1-12167129-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.44
- MetaLR 0.75
- MetaSVM 0.05
- CADD 24.40
- PolyPhen-2 0.76
- SIFT 0.09
- Population evidence available
- Structural context available
- Literature evidence available