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BRCA1 c.5332+78C>A
Variant ID: 17-41203002-G-T
NM_007294.3(
BRCA1
):c.5332+78C>A
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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: 5332+78C>A
PubMed Link:
35456503
Variant Present in the following documents:
genes-13-00697.pdf
View BVdb publication page