S56T (p.Ser56Thr) variant of TNFRSF1A (P19438)
S56T (p.Ser56Thr) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
S56T (p.Ser56Thr) variant details
- p.Ser56Thr
- ExAC rs770344578
- gnomAD rs770344578
- Missense
- Variant Prioritization Score for Impact Estimate 0.346
- REVEL 0.48
- CADD 5.56
- PolyPhen-2 0.02
- SIFT 0.36
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available