M31T (p.Met31Thr) variant of TNFRSF13B (O14836)
M31T (p.Met31Thr) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data.
M31T (p.Met31Thr) variant details
- p.Met31Thr
- ExAC rs757910034
- gnomAD rs757910034
- Missense
- Variant Prioritization Score for Impact Estimate 0.617
- REVEL 0.69
- CADD 23.30
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00012)