Varaico: Literature-Extracted Genetic Variants

Gene:BRCA2
Variant:p.P26R
Back to variants list

BRCA2

NM_000059.4:p.P26R

Associated Papers

Precision screening facilitates clinical classification of BRCA2-PALB2 binding variants with benign and pathogenic functional effects.

Bose M et al.

The Journal of Clinical Investigation, 2025

Understanding and predicting the functional consequences of missense mutations in BRCA1 and BRCA2.

Aljarf R et al.

Scientific Reports, 2022

35729312 (PubMed )
Supplement: 41598_2022_13508_MOESM2_ESM.xlsx › Sheet1

Genomic mutation features identify distinct BRCA-associated mutation characteristics in endometrioid carcinoma and endometrioid ovarian carcinoma.

Cao C et al.

Aging, 2021

34837690 (PubMed )
Supplement: aging-13-203710-s004.xlsx › Sheet1

C77G in PTPRC (CD45) is no risk allele for ovarian cancer, but associated with less aggressive disease.

Landskron J et al.

Plos One, 2017

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."