F78S (p.Phe78Ser) variant of TNFRSF13B (O14836)
F78S (p.Phe78Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data.
F78S (p.Phe78Ser) variant details
- p.Phe78Ser
- gnomAD rs1197261395
- Missense
- Variant Prioritization Score for Impact Estimate 0.504
- REVEL 0.51
- CADD 22.50
- PolyPhen-2 0.22
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00041)