P26A (p.Pro26Ala) variant of AIP (AH receptor-interacting protein)
P26A (p.Pro26Ala) in AIP (AH receptor-interacting protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided; Hereditary cancer-predisposing syndrome. The record also includes published literature and structural context.
P26A (p.Pro26Ala) variant details
- p.Pro26Ala
- rs2495387918
- ClinGen CA381545849
- ClinVar RCV003709622
- ClinVar RCV005575209
- Uncertain significance
- not provided; Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (not provided; 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)