BRCA2 c.4453dup ;(p.I1485Nfs*3)

Variant ID: 13-32912944-C-CA

NM_000059.3(BRCA2):c.4453dup;(p.I1485Nfs*3)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: BRCA2: 4453_4454insA
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 4
View BVdb publication page



Characteristics of BRCA1/2 pathogenic germline mutations in chinese NSCLC patients and a comparison with HBOC.

Hereditary Cancer In Clinical Practice
Xu, Zheyuan Z; Wang, Yang Y; Wang, Lan L; Cui, Fengxian F; Zhang, Libin L; Xiong, Jian J; Peng, Hao H
Publication Date: 2021-02-09

Variant appearance in text: BRCA2: I1485Nfs*3
PubMed Link: 33563323
Variant Present in the following documents:
  • Main text
  • 13053_2021_Article_174.pdf
View BVdb publication page