Q58H (p.Gln58His) variant of TNFRSF13C (Q96RJ3)
Q58H (p.Gln58His) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and published literature.
Q58H (p.Gln58His) variant details
- p.Gln58His
- gnomAD 22-41926294-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.144
- REVEL 0.03
- MetaLR 0.05
- MetaSVM -1.06
- CADD 11.80
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Literature evidence available