S13G (p.Ser13Gly) variant of TNFRSF13B (O14836)
S13G (p.Ser13Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data.
S13G (p.Ser13Gly) variant details
- p.Ser13Gly
- TOPMed rs1452918381
- Missense
- Variant Prioritization Score for Impact Estimate 0.376
- REVEL 0.20
- CADD 13.20
- PolyPhen-2 0.00
- SIFT 0.43
- Most common in the African/African-American population (allele frequency 4.8e-05)