G13A (p.Gly13Ala) variant of TNFRSF1B (P20333)
G13A (p.Gly13Ala) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
G13A (p.Gly13Ala) variant details
- p.Gly13Ala
- gnomAD 1-12167129-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.324
- REVEL 0.30
- MetaLR 0.61
- MetaSVM -0.19
- CADD 21.00
- PolyPhen-2 0.31
- SIFT 0.36
- Population evidence available
- Structural context available
- Literature evidence available