D38N (p.Asp38Asn) variant of TNFRSF9 (Q07011)
D38N (p.Asp38Asn) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
D38N (p.Asp38Asn) variant details
- p.Asp38Asn
- ExAC rs761651539
- gnomAD rs761651539
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.05
- CADD 16.50
- PolyPhen-2 0.00
- SIFT 0.09
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available