D119G (p.Asp119Gly) variant of TNFRSF9 (Q07011)
D119G (p.Asp119Gly) 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.
D119G (p.Asp119Gly) variant details
- p.Asp119Gly
- gnomAD 1-7937747-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- REVEL 0.14
- CADD 23.90
- PolyPhen-2 0.20
- SIFT 0.03
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available