P7A (p.Pro7Ala) variant of TNFRSF1A (P19438)
P7A (p.Pro7Ala) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
P7A (p.Pro7Ala) variant details
- p.Pro7Ala
- ExAC rs200727600
- TOPMed rs200727600
- gnomAD rs200727600
- Missense
- Variant Prioritization Score for Impact Estimate 0.552
- REVEL 0.64
- CADD 22.20
- PolyPhen-2 0.15
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available