C62Y (p.Cys62Tyr) variant of TNFRSF13B (O14836)
C62Y (p.Cys62Tyr) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
C62Y (p.Cys62Tyr) variant details
- p.Cys62Tyr
- TOPMed rs1410473109
- gnomAD rs1410473109
- Missense
- Variant Prioritization Score for Impact Estimate 0.752
- REVEL 0.74
- CADD 24.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available