S78F (p.Ser78Phe) variant of TNFRSF4 (P43489)
S78F (p.Ser78Phe) in TNFRSF4 (P43489) 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.
S78F (p.Ser78Phe) variant details
- p.Ser78Phe
- ExAC rs750629113
- TOPMed rs750629113
- gnomAD rs750629113
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.29
- CADD 21.00
- PolyPhen-2 0.54
- SIFT 0.04
- Most common in the African/African-American population (allele frequency 7.2e-05)