H98N (p.His98Asn) variant of TNFRSF1A (P19438)
H98N (p.His98Asn) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
H98N (p.His98Asn) variant details
- p.His98Asn
- ExAC rs755815269
- gnomAD rs755815269
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.18
- CADD 12.40
- PolyPhen-2 0.01
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available