A18T (p.Ala18Thr) variant of TNFRSF1B (P20333)
A18T (p.Ala18Thr) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
A18T (p.Ala18Thr) variant details
- p.Ala18Thr
- Ensembl rs1039748824
- Missense
- Variant Prioritization Score for Impact Estimate 0.334
- REVEL 0.29
- MetaLR 0.63
- MetaSVM -0.13
- CADD 15.10
- PolyPhen-2 0.19
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 2.1e-06)
- Structural context available