A19P (p.Ala19Pro) variant of TNFRSF1B (P20333)
A19P (p.Ala19Pro) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data, published literature, and structural context.
A19P (p.Ala19Pro) variant details
- p.Ala19Pro
- gnomAD 1-12167146-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.448
- REVEL 0.57
- MetaLR 0.62
- MetaSVM -0.39
- CADD 14.80
- PolyPhen-2 0.00
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 4.1e-06)
- Structural context available
- Literature evidence available