S78T (p.Ser78Thr) variant of TNFRSF4 (P43489)
S78T (p.Ser78Thr) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
S78T (p.Ser78Thr) variant details
- p.Ser78Thr
- ExAC rs756177147
- TOPMed rs756177147
- gnomAD rs756177147
- Missense
- Variant Prioritization Score for Impact Estimate 0.307
- REVEL 0.27
- CADD 13.80
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the African/African-American population (allele frequency 7.2e-05)