BRCA1 c.4986+3G>A

Variant ID: 17-41222942-C-T

NM_007294.3(BRCA1):c.4986+3G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A CRISPR-based base-editing screen for the functional assessment of BRCA1 variants.

Oncogene
Kweon, Jiyeon J; Jang, An-Hee AH; Shin, Ha Rim HR; See, Ji-Eun JE; Lee, Woochang W; Lee, Jong Won JW; Chang, Suhwan S; Kim, Kyunggon K; Kim, Yongsub Y
Publication Date: 2020-01

Variant appearance in text: BRCA1: 4986+3G>A
PubMed Link: 31467430
Variant Present in the following documents:
  • Main text
  • 41388_2019_Article_968.pdf
View BVdb publication page



Accurate classification of BRCA1 variants with saturation genome editing.

Nature
Findlay, Gregory M GM; Daza, Riza M RM; Martin, Beth B; Zhang, Melissa D MD; Leith, Anh P AP; Gasperini, Molly M; Janizek, Joseph D JD; Huang, Xingfan X; Starita, Lea M LM; Shendure, Jay J
Publication Date: 2018-10

Variant appearance in text: BRCA1: 4986+3G>A
PubMed Link: 30209399
Variant Present in the following documents:
  • NIHMS1501643-supplement-2.xlsx, sheet 1
View BVdb publication page