T35A (p.Thr35Ala) variant of TNFRSF9 (Q07011)
T35A (p.Thr35Ala) in TNFRSF9 (Q07011) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
T35A (p.Thr35Ala) variant details
- p.Thr35Ala
- NCI-TCGA Cosmic COSV1010
- cosmic curated COSV10109
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.371
- REVEL 0.18
- CADD 25.50
- PolyPhen-2 0.86
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available