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BRCA2 c.2685_2686del ;(p.N896*)
Variant ID: 13-32911177-CTA-C
NM_000059.3(
BRCA2
):c.2685_2686del;(p.N896*)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa.
Bmc Cancer
ElBiad, Oubaida O; Laraqui, Abdelilah A; El Boukhrissi, Fatima F; Mounjid, Chaimaa C; Lamsisi, Maryame M; Bajjou, Tahar T; Elannaz, Hicham H; Lahlou, Amine Idriss AI; Kouach, Jaouad J; Benchekroune, Khadija K; Oukabli, Mohammed M; Chahdi, Hafsa H; Ennaji, Moulay Mustapha MM; Tanz, Rachid R; Sbitti, Yassir Y; Ichou, Mohammed M; Ennibi, Khalid K; Badaoui, Bouabid B; Sekhsokh, Yassine Y
Publication Date: 2022-02-25
Variant appearance in text: BRCA2: 2685_2686del
PubMed Link:
35216584
Variant Present in the following documents:
Main text
12885_2022_Article_9181.pdf
View BVdb publication page
Towards population-based genetic screenings for breast and ovarian cancer: A comprehensive review from economic evaluations to patient perspectives.
Breast (Edinburgh, Scotland)
Ficarazzi, Filomena F; Vecchi, Manuela M; Ferrari, Maurizio M; Pierotti, Marco A MA
Publication Date: 2021-08
Variant appearance in text: BRCA2: 2685_2686del
PubMed Link:
34022715
Variant Present in the following documents:
main.pdf
View BVdb publication page