S62A (p.Ser62Ala) variant of TNFRSF13C (Q96RJ3)
S62A (p.Ser62Ala) 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.
S62A (p.Ser62Ala) variant details
- p.Ser62Ala
- gnomAD 22-41926284-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.138
- REVEL 0.01
- MetaLR 0.04
- MetaSVM -1.05
- CADD 16.80
- PolyPhen-2 0.15
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Literature evidence available