D119N (p.Asp119Asn) variant of TNFRSF9 (Q07011)
D119N (p.Asp119Asn) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
D119N (p.Asp119Asn) variant details
- p.Asp119Asn
- gnomAD 1-7937748-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.04
- CADD 22.90
- PolyPhen-2 0.02
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available