P71R (p.Pro71Arg) variant of FOS (Protein c-Fos)
P71R (p.Pro71Arg) in FOS (Protein c-Fos) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
P71R (p.Pro71Arg) variant details
- p.Pro71Arg
- TOPMed rs1000193997
- gnomAD rs1000193997
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.47
- REVEL 0.34
- MetaLR 0.39
- MetaSVM -0.25
- CADD 26.50
- PolyPhen-2 0.95
- SIFT 0.05
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available