Q28P (p.Gln28Pro) variant of PRKAR1A (P10644)
Q28P (p.Gln28Pro) in PRKAR1A (P10644) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Carney complex, type 1. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes published literature and structural context.
Q28P (p.Gln28Pro) variant details
- p.Gln28Pro
- rs1600462191
- ClinGen CA400751932
- ClinVar RCV001017705
- ClinVar RCV002304225
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Carney complex, type 1
- Missense
- Variant Prioritization Score for Impact Estimate 0.697
- AlphaMissense 0.61
- MetaLR 0.66
- MetaSVM 0.39
- PolyPhen-2 0.99
- SIFT 0.01
- MutPred 0.66
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Carney complex, type 1)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Carney Complex. (PMID 20301463)
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)