D36N (p.Asp36Asn) variant of TNFRSF1A (P19438)
D36N (p.Asp36Asn) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data and structural context.
D36N (p.Asp36Asn) variant details
- p.Asp36Asn
- TOPMed rs1469655659
- gnomAD rs1469655659
- Missense
- Variant Prioritization Score for Impact Estimate 0.538
- REVEL 0.44
- CADD 13.10
- PolyPhen-2 0.00
- SIFT 0.16
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available