BRCA2 c.8754+526C>T

Variant ID: 13-32951454-C-T

NM_000059.3(BRCA2):c.8754+526C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: BRCA2: 8754+526C>T; rs9567623
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Hereditary breast cancer in the Han Chinese population.

Journal Of Epidemiology
Cao, Wenming W; Wang, Xiaojia X; Li, Ji-Cheng JC
Publication Date: 2013

Variant appearance in text: rs9567623
PubMed Link: 23318652
Variant Present in the following documents:
  • Main text
  • je-23-075.pdf
View BVdb publication page