BRCA2 c.676del ;(p.T226Lfs*4)

Variant ID: 13-32903624-TA-T

NM_000059.3(BRCA2):c.676del;(p.T226Lfs*4)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Array genotyping as diagnostic approach in medical genetics.

Molecular Genetics & Genomic Medicine
Witsch-Baumgartner, Martina M; Schwaninger, Gunda G; Schnaiter, Simon S; Kollmann, Franziska F; Burkhard, Silja S; Gröbner, Rebekka R; Mühlegger, Beatrix B; Schamschula, Esther E; Kirchmeier, Peter P; Zschocke, Johannes J
Publication Date: 2022-09

Variant appearance in text: BRCA2: 676del
PubMed Link: 35912641
Variant Present in the following documents:
  • MGG3-10-e2016.pdf
View BVdb publication page



Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.

Bmc Medicine
Haverfield, Eden V EV; Esplin, Edward D ED; Aguilar, Sienna J SJ; Hatchell, Kathryn E KE; Ormond, Kelly E KE; Hanson-Kahn, Andrea A; Atwal, Paldeep S PS; Macklin-Mantia, Sarah S; Hines, Stephanie S; Sak, Caron W-M CW; Tucker, Steven S; Bleyl, Steven B SB; Hulick, Peter J PJ; Gordon, Ora K OK; Velsher, Lea L; Gu, Jessica Y J JYJ; Weissman, Scott M SM; Kruisselbrink, Teresa T; Abel, Christopher C; Kettles, Michele M; Slavotinek, Anne A; Mendelsohn, Bryce A BA; Green, Robert C RC; Aradhya, Swaroop S; Nussbaum, Robert L RL
Publication Date: 2021-08-18

Variant appearance in text: BRCA2: 676del
PubMed Link: 34404389
Variant Present in the following documents:
  • 12916_2021_1999_MOESM2_ESM.pdf
View BVdb publication page



Application of cell-free DNA for genomic tumor profiling: a feasibility study.

Oncotarget
Ahlborn, Lise B LB; Rohrberg, Kristoffer S KS; Gabrielaite, Migle M; Tuxen, Ida V IV; Yde, Christina W CW; Spanggaard, Iben I; Santoni-Rugiu, Eric E; Nielsen, Finn C FC; Lassen, Ulrik U; Mau-Sorensen, Morten M; Østrup, Olga O
Publication Date: 2019-02-15

Variant appearance in text: N/A
PubMed Link: 30858924
Variant Present in the following documents:
View BVdb publication page



Germline variation in BRCA1/2 is highly ethnic-specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients.

International Journal Of Cancer
Bhaskaran, Shanmuga Priya SP; Chandratre, Khyati K; Gupta, Hemant H; Zhang, Li L; Wang, Xiaoyu X; Cui, Jian J; Kim, Yeong C YC; Sinha, Siddharth S; Jiang, Luhan L; Lu, Boya B; Wu, Xiaobing X; Qin, Zixin Z; Huang, Teng T; Wang, San Ming SM
Publication Date: 2019-08-15

Variant appearance in text: BRCA2: 676del
PubMed Link: 30702160
Variant Present in the following documents:
  • IJC-145-962-s007.xlsx, sheet 2
View BVdb publication page