D36H (p.Asp36His) variant of TNFRSF1A (P19438)
D36H (p.Asp36His) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
D36H (p.Asp36His) variant details
- p.Asp36His
- TOPMed rs1469655659
- gnomAD rs1469655659
- Missense
- Variant Prioritization Score for Impact Estimate 0.655
- REVEL 0.65
- CADD 12.80
- PolyPhen-2 0.03
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available