P26Q (p.Pro26Gln) variant of BRCA2 (P51587)
P26Q (p.Pro26Gln) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance.
P26Q (p.Pro26Gln) variant details
- p.Pro26Gln
- TOPMed rs1566215668
- gnomAD rs1566215668
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance