A64G (p.Ala64Gly) variant of TNFRSF13B (O14836)
A64G (p.Ala64Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
A64G (p.Ala64Gly) variant details
- p.Ala64Gly
- ESP rs145002378
- ExAC rs145002378
- TOPMed rs145002378
- gnomAD rs145002378
- Missense
- Variant Prioritization Score for Impact Estimate 0.288
- REVEL 0.25
- CADD 19.70
- PolyPhen-2 0.30
- SIFT 0.06
- Most common in the African/African-American population (allele frequency 0.00031)
- Structural context available