R67M (p.Arg67Met) variant of TNFRSF13B (O14836)
R67M (p.Arg67Met) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
R67M (p.Arg67Met) variant details
- p.Arg67Met
- gnomAD rs1363140258
- Missense
- Variant Prioritization Score for Impact Estimate 0.338
- REVEL 0.36
- CADD 24.20
- PolyPhen-2 0.48
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00041)