D41V (p.Asp41Val) variant of TNFRSF1A (P19438)
D41V (p.Asp41Val) in TNFRSF1A (P19438) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes structural context.
D41V (p.Asp41Val) variant details
- p.Asp41Val
- rs2136823142
- ClinGen CA383551036
- ClinVar RCV001509418
- Ensembl rs2136823142
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.697
- AlphaMissense 0.24
- MetaLR 0.89
- MetaSVM 0.52
- PolyPhen-2 0.48
- SIFT 0.02
- EVE 0.77
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available