R35G (p.Arg35Gly) variant of F2 (Prothrombin)
R35G (p.Arg35Gly) in F2 (Prothrombin) 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 0.40 / 1. The record also includes population frequency data and structural context.
R35G (p.Arg35Gly) variant details
- p.Arg35Gly
- rs144785536
- NCI-TCGA Cosmic COSV6131
- cosmic curated COSV61314
- 1000Genomes rs144785536
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.27
- CADD 14.70
- PolyPhen-2 0.00
- SIFT 0.21
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available