R10P (p.Arg10Pro) variant of TNFRSF4 (P43489)
R10P (p.Arg10Pro) in TNFRSF4 (P43489) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data.
R10P (p.Arg10Pro) variant details
- p.Arg10Pro
- ExAC rs774474644
- TOPMed rs774474644
- gnomAD rs774474644
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.0824
- REVEL 0.11
- CADD 0.12
- PolyPhen-2 0.00
- SIFT 0.08
- EBI: Variant of uncertain significance (in dbSNP:rs35304565)
- UniProt: Uncertain significance (in dbSNP:rs35304565)
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)