Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRCA2 c.668dup ;(p.H223Qfs*2)
Variant ID: 13-32903615-C-CA
NM_000059.3(
BRCA2
):c.668dup;(p.H223Qfs*2)
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:
Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers.
Frontiers In Oncology
Hamdi, Yosr Y; Mighri, Najah N; Boujemaa, Maroua M; Mejri, Nesrine N; Ben Nasr, Sonia S; Ben Rekaya, Mariem M; Messaoud, Olfa O; Bouaziz, Hanen H; Berrazega, Yosra Y; Rachdi, Haifa H; Jaidane, Olfa O; Daoud, Nouha N; Zribi, Aref A; Ayari, Jihene J; El Benna, Houda H; Labidi, Soumaya S; Ben Hassouna, Jamel J; Haddaoui, Abderazzek A; Rahal, Khaled K; Benna, Farouk F; Mrad, Ridha R; Ben Ahmed, Slim S; Boussen, Hamouda H; Boubaker, Samir S; Abdelhak, Sonia S
Publication Date: 2021
Variant appearance in text: BRCA2: 668dupA
PubMed Link:
34490083
Variant Present in the following documents:
fonc-11-674965.pdf
View BVdb publication page