BRCA1 c.5152+80del

Variant ID: 17-41215810-AC-A

NM_007294.3(BRCA1):c.5152+80del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 Variants.

Genes
Alenezi, Wejdan M WM; Fierheller, Caitlin T CT; Revil, Timothée T; Serruya, Corinne C; Mes-Masson, Anne-Marie AM; Foulkes, William D WD; Provencher, Diane D; El Haffaf, Zaki Z; Ragoussis, Jiannis J; Tonin, Patricia N PN
Publication Date: 2022-04-15

Variant appearance in text: BRCA1: 5152+80del
PubMed Link: 35456503
Variant Present in the following documents:
  • genes-13-00697.pdf
View BVdb publication page