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BRCA2 c.4376dup ;(p.N1459Kfs*7)
Variant ID: 13-32912866-T-TA
NM_000059.3(
BRCA2
):c.4376dup;(p.N1459Kfs*7)
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:
Importance of multigene panel test in patients with consanguineous marriage and family history of breast cancer.
Oncology Letters
Ozmen, Vahit V; Caglayan, Ahmet Okay AO; Yararbas, Kanay K; Ordu, Cetin C; Aktepe, Fatma F; Ozmen, Tolga T; Ilgun, Ahmet Serkan AS; Soybir, Gursel G; Alco, Gul G; Tsaousis, Georgios N GN; Papadopoulou, Eirini E; Agiannitopoulos, Konstantinos K; Pepe, Georgia G; Kampouri, Stavroula S; Nasioulas, George G; Sezgin, Efe E; Soran, Atilla A
Publication Date: 2022-04
Variant appearance in text: BRCA2: 4376dupA
PubMed Link:
35261632
Variant Present in the following documents:
ol-23-04-13238.pdf
View BVdb publication page