P26S (p.Pro26Ser) variant of BRCA2 (P51587)
P26S (p.Pro26Ser) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes variant effect predictions and published literature.
P26S (p.Pro26Ser) variant details
- p.Pro26Ser
- rs2138703603
- ClinGen CA387754044
- ClinVar RCV002257063
- Ensembl rs2138703603
- Uncertain significance
- Missense
- AlphaMissense 0.51
- MetaLR 0.08
- MetaSVM -1.18
- SIFT 0.00
- MutPred 0.49
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)