Q99P (p.Gln99Pro) variant of TNFRSF13B (O14836)
Q99P (p.Gln99Pro) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
Q99P (p.Gln99Pro) variant details
- p.Gln99Pro
- gnomAD rs1375800035
- Missense
- Variant Prioritization Score for Impact Estimate 0.526
- REVEL 0.50
- CADD 15.30
- PolyPhen-2 0.31
- SIFT 0.11
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available