P23R (p.Pro23Arg) variant of RB1 (P06400)
P23R (p.Pro23Arg) in RB1 (P06400) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes published literature and structural context.
P23R (p.Pro23Arg) variant details
- p.Pro23Arg
- rs1952053594
- ClinGen CA388250260
- ClinVar RCV002362317
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.417
- AlphaMissense 0.11
- MetaLR 0.42
- MetaSVM -0.60
- PolyPhen-2 0.01
- SIFT 0.04
- MutPred 0.32
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)