BRCA2 c.-40+222C>T

Variant ID: 13-32890026-C-T

NM_000059.4(BRCA2):c.-40+222C>T

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Single nucleotide polymorphisms and the risk of developing a second primary cancer among head and neck cancer patients: a systematic literature review and meta-analysis.

Bmc Cancer
Hoxhaj, Ilda I; Vukovic, Vladimir V; Boccia, Stefania S; Pastorino, Roberta R
Publication Date: 2021-06-02

Variant appearance in text: rs9562605
PubMed Link: 34078296
Variant Present in the following documents:
  • Main text
  • 12885_2021_Article_8335.pdf
View BVdb publication page



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: -40+222C>T; rs9562605
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



A Chinese family affected by lynch syndrome caused by MLH1 mutation.

Bmc Medical Genetics
Jia, Shuqin S; Zhang, Meng M; Sun, Yu Y; Yan, Hai H; Zhao, Fangping F; Li, Ziyu Z; Ji, Jiafu J
Publication Date: 2018-06-22

Variant appearance in text: BRCA2: -40+222C>T; rs9562605
PubMed Link: 29929473
Variant Present in the following documents:
  • 12881_2018_605_MOESM2_ESM.xlsx, sheet 1
  • 12881_2018_605_MOESM2_ESM.xlsx, sheet 2
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: rs9562605
PubMed Link: 21161372
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs9562605
PubMed Link: 20522537
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants.

Cancer Prevention Research (Philadelphia, Pa.)
Wu, Xifeng X; Spitz, Margaret R MR; Lee, J Jack JJ; Lippman, Scott M SM; Ye, Yuanqing Y; Yang, Hushan H; Khuri, Fadlo R FR; Kim, Edward E; Gu, Jian J; Lotan, Reuben R; Hong, Waun K WK
Publication Date: 2009-07

Variant appearance in text: rs9562605
PubMed Link: 19584075
Variant Present in the following documents:
  • Main text
View BVdb publication page



LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.

Bmc Genetics
Chang, Hsueh-Wei HW; Chuang, Li-Yeh LY; Chang, Yan-Jhu YJ; Cheng, Yu-Huei YH; Hung, Yu-Chen YC; Chen, Hsiang-Chi HC; Yang, Cheng-Hong CH
Publication Date: 2009-06-06

Variant appearance in text: rs9562605
PubMed Link: 19500380
Variant Present in the following documents:
  • Main text
  • 1471-2156-10-26.pdf
View BVdb publication page