A15T (p.Ala15Thr) variant of TNFRSF4 (P43489)
A15T (p.Ala15Thr) in TNFRSF4 (P43489) 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 0.36 / 1. The record also includes population frequency data.
A15T (p.Ala15Thr) variant details
- p.Ala15Thr
- rs1269060561
- NCI-TCGA Cosmic COSV5541
- gnomAD rs1269060561
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.361
- REVEL 0.26
- CADD 22.70
- PolyPhen-2 0.99
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 2.4e-05)