D26N (p.Asp26Asn) variant of TNFRSF9 (Q07011)
D26N (p.Asp26Asn) 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 0.25 / 1. The record also includes population frequency data and structural context.
D26N (p.Asp26Asn) variant details
- p.Asp26Asn
- NCI-TCGA Cosmic COSV1010
- cosmic curated COSV10109
- 1000Genomes rs2151420715
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.13
- CADD 11.50
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available