S88G (p.Ser88Gly) variant of TNFRSF13B (O14836)
S88G (p.Ser88Gly) in TNFRSF13B (O14836) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data.
S88G (p.Ser88Gly) variant details
- p.Ser88Gly
- gnomAD rs2087568984
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.667
- REVEL 0.70
- CADD 24.20
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Most common in the 1KG:CLM population (allele frequency 0.0053)