BRCA2 c.67+1042A>C

Variant ID: 13-32891706-A-C

NM_000059.3(BRCA2):c.67+1042A>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


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: rs206120
PubMed Link: 29929473
Variant Present in the following documents:
  • 12881_2018_605_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium.

Carcinogenesis
Kazma, Rémi R; Babron, Marie-Claude MC; Gaborieau, Valérie V; Génin, Emmanuelle E; Brennan, Paul P; Hung, Rayjean J RJ; McLaughlin, John R JR; Krokan, Hans E HE; Elvestad, Maiken B MB; Skorpen, Frank F; Anderssen, Endre E; Vooder, Tõnu T; Välk, Kristjan K; Metspalu, Andres A; Field, John K JK; Lathrop, Mark M; Sarasin, Alain A; Benhamou, Simone S; ,
Publication Date: 2012-05

Variant appearance in text: rs206120
PubMed Link: 22382497
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: rs206120
PubMed Link: 19500380
Variant Present in the following documents:
  • Main text
  • 1471-2156-10-26.pdf
View BVdb publication page