BRCA1 c.5093_5096del ;(p.E1698Gfs*3)

Variant ID: 17-41215946-CCGTT-C

NM_007294.3(BRCA1):c.5093_5096del;(p.E1698Gfs*3)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Integrative Analysis of Germline Rare Variants in Clear and Non-Clear Cell Renal Cell Carcinoma.

Medrxiv : The Preprint Server For Health Sciences
Han, Seunghun S; Camp, Sabrina Y SY; Chu, Hoyin H; Collins, Ryan R; Gillani, Riaz R; Park, Jihye J; Bakouny, Ziad Z; Ricker, Cora A CA; Reardon, Brendan B; Moore, Nicholas N; Kofman, Eric E; Labaki, Chris C; Braun, David D; Choueiri, Toni K TK; AlDubayan, Saud H SH; Van Allen, Eliezer M EM
Publication Date: 2023-01-19

Variant appearance in text: BRCA1: 5093_5096del
PubMed Link: 36712083
Variant Present in the following documents:
  • media-1.xlsx, sheet 5
View BVdb publication page



Integrating a Next Generation Sequencing Panel into Clinical Practice in Ovarian Cancer.

Yonsei Medical Journal
Lee, Yong Jae YJ; Kim, Dachan D; Kim, Hyun Soo HS; Na, Kiyong K; Lee, Jung Yun JY; Nam, Eun Ji EJ; Kim, Sang Wun SW; Kim, Sunghoon S; Kim, Young Tae YT
Publication Date: 2019-10

Variant appearance in text: BRCA1: 5093_5096del
PubMed Link: 31538426
Variant Present in the following documents:
  • Main text
  • ymj-60-914.pdf
View BVdb publication page