R3Q (p.Arg3Gln) variant of TNFRSF13C (Q96RJ3)
R3Q (p.Arg3Gln) in TNFRSF13C (Q96RJ3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data.
R3Q (p.Arg3Gln) variant details
- p.Arg3Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.01
- CADD 7.08
- PolyPhen-2 0.01
- SIFT 0.22
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 0.00015)