BRCA2 c.7007+1298A>C

Variant ID: 13-32922331-A-C

NM_000059.3(BRCA2):c.7007+1298A>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Gene networks and expression quantitative trait loci associated with adjuvant chemotherapy response in high-grade serous ovarian cancer.

Bmc Cancer
Choi, Jihoon J; Topouza, Danai G DG; Tarnouskaya, Anastasiya A; Nesdoly, Sean S; Koti, Madhuri M; Duan, Qing Ling QL
Publication Date: 2020-05-13

Variant appearance in text: rs11571686
PubMed Link: 32404140
Variant Present in the following documents:
  • Main text
  • 12885_2020_Article_6922.pdf
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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: 7007+1298A>C; rs11571686
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status.

Breast Cancer Research And Treatment
Figueiredo, Jane C JC; Brooks, Jennifer D JD; Conti, David V DV; Poynter, Jenny N JN; Teraoka, Sharon N SN; Malone, Kathleen E KE; Bernstein, Leslie L; Lee, Won D WD; Duggan, David J DJ; Siniard, Ashley A; Concannon, Patrick P; Capanu, Marinela M; Lynch, Charles F CF; Olsen, Jørgen H JH; Haile, Robert W RW; Bernstein, Jonine L JL
Publication Date: 2011-06

Variant appearance in text: rs11571686
PubMed Link: 21161372
Variant Present in the following documents:
  • Main text
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Variation within DNA repair pathway genes and risk of multiple sclerosis.

American Journal Of Epidemiology
Briggs, Farren B S FB; Goldstein, Benjamin A BA; McCauley, Jacob L JL; Zuvich, Rebecca L RL; De Jager, Philip L PL; Rioux, John D JD; Ivinson, Adrian J AJ; Compston, Alastair A; Hafler, David A DA; Hauser, Stephen L SL; Oksenberg, Jorge R JR; Sawcer, Stephen J SJ; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Barcellos, Lisa F LF; ,
Publication Date: 2010-07-15

Variant appearance in text: rs11571686
PubMed Link: 20522537
Variant Present in the following documents:
  • Main text
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Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.

Breast Cancer Research : Bcr
Baynes, Caroline C; Healey, Catherine S CS; Pooley, Karen A KA; Scollen, Serena S; Luben, Robert N RN; Thompson, Deborah J DJ; Pharoah, Paul D P PD; Easton, Douglas F DF; Ponder, Bruce A J BA; Dunning, Alison M AM; ,
Publication Date: 2007

Variant appearance in text: rs11571686
PubMed Link: 17428325
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between common variation in 120 candidate genes and breast cancer risk.

Plos Genetics
Pharoah, Paul D P PD; Tyrer, Jonathan J; Dunning, Alison M AM; Easton, Douglas F DF; Ponder, Bruce A J BA; ,
Publication Date: 2007-03-16

Variant appearance in text: rs11571686
PubMed Link: 17367212
Variant Present in the following documents:
View BVdb publication page