A67V (p.Ala67Val) variant of TNFRSF13C (Q96RJ3)
A67V (p.Ala67Val) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
A67V (p.Ala67Val) variant details
- p.Ala67Val
- TOPMed rs1392495883
- gnomAD rs1392495883
- Missense
- Variant Prioritization Score for Impact Estimate 0.204
- REVEL 0.03
- CADD 6.94
- PolyPhen-2 0.02
- SIFT 0.45
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)