A111T (p.Ala111Thr) variant of TNFRSF4 (P43489)
A111T (p.Ala111Thr) 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 0.18 / 1. The record also includes population frequency data and structural context.
A111T (p.Ala111Thr) variant details
- p.Ala111Thr
- rs1423127792
- NCI-TCGA Cosmic COSV9976
- TOPMed rs1423127792
- gnomAD rs1423127792
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.05
- CADD 18.60
- PolyPhen-2 0.01
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available