M31R (p.Met31Arg) variant of TNFRSF13B (O14836)
M31R (p.Met31Arg) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data.
M31R (p.Met31Arg) variant details
- p.Met31Arg
- ExAC rs757910034
- gnomAD rs757910034
- Missense
- Variant Prioritization Score for Impact Estimate 0.634
- REVEL 0.71
- CADD 23.90
- PolyPhen-2 0.97
- SIFT 0.00
- Most common in the 1KG:CLM population (allele frequency 0.0053)