RAD51 c.87+110A>G

Variant ID: 15-40991153-A-G

NM_002875.4(RAD51):c.87+110A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.

Molecular Medicine Reports
Li, Yiqiang Y; Lin, Xuemei X; Zhu, Mingwei M; Li, Jingchun J; Yuan, Zhe Z; Xu, Hongwen H
Publication Date: 2020-09

Variant appearance in text: rs2304579
PubMed Link: 32705272
Variant Present in the following documents:
  • Supplementary_Data1.xlsx, sheet 1
View BVdb publication page



Modification of PARP4, XRCC3, and RAD51 Gene Polymorphisms on the Relation between Bisphenol A Exposure and Liver Abnormality.

International Journal Of Environmental Research And Public Health
Kim, Jin Hee JH; Hong, Yun-Chul YC
Publication Date: 2020-04-17

Variant appearance in text: RAD51: 87+110A>G; rs2304579
PubMed Link: 32316696
Variant Present in the following documents:
  • Main text
  • ijerph-17-02794.pdf
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs2304579
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs2304579
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



Genetic susceptibility in childhood acute leukaemias: a systematic review.

Ecancermedicalscience
Brisson, Gisele D GD; Alves, Liliane R LR; Pombo-de-Oliveira, Maria S MS
Publication Date: 2015

Variant appearance in text: rs2304579
PubMed Link: 26045716
Variant Present in the following documents:
  • Main text
View BVdb publication page



RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families.

Springerplus
Pelttari, Liisa M LM; Kiiski, Johanna I JI; Ranta, Salla S; Vilske, Sara S; Blomqvist, Carl C; Aittomäki, Kristiina K; Nevanlinna, Heli H
Publication Date: 2015

Variant appearance in text: rs2304579
PubMed Link: 25918678
Variant Present in the following documents:
  • Main text
  • 40064_2015_Article_880.pdf
View BVdb publication page



Non-Hodgkin lymphoma risk and variants in genes controlling lymphocyte development.

Plos One
Schuetz, Johanna M JM; Daley, Denise D; Leach, Stephen S; Conde, Lucia L; Berry, Brian R BR; Gallagher, Richard P RP; Connors, Joseph M JM; Gascoyne, Randy D RD; Bracci, Paige M PM; Skibola, Christine F CF; Spinelli, John J JJ; Brooks-Wilson, Angela R AR
Publication Date: 2013

Variant appearance in text: rs2304579
PubMed Link: 24098683
Variant Present in the following documents:
  • pone.0075170.s001.xls, sheet 1
View BVdb publication page



Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia.

Cancer Causes & Control : Ccc
Chokkalingam, Anand P AP; Bartley, Karen K; Wiemels, Joseph L JL; Metayer, Catherine C; Barcellos, Lisa F LF; Hansen, Helen M HM; Aldrich, Melinda C MC; Guha, Neela N; Urayama, Kevin Y KY; Scélo, Ghislaine G; Chang, Jeffrey S JS; Month, Stacy R SR; Wiencke, John K JK; Buffler, Patricia A PA
Publication Date: 2011-12

Variant appearance in text: rs2304579
PubMed Link: 21987080
Variant Present in the following documents:
  • Main text
  • 10552_2011_Article_9848.pdf
View BVdb publication page



RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.

American Journal Of Human Genetics
Antoniou, Antonis C AC; Sinilnikova, Olga M OM; Simard, Jacques J; Léoné, Mélanie M; Dumont, Martine M; Neuhausen, Susan L SL; Struewing, Jeffery P JP; Stoppa-Lyonnet, Dominique D; Barjhoux, Laure L; Hughes, David J DJ; Coupier, Isabelle I; Belotti, Muriel M; Lasset, Christine C; Bonadona, Valérie V; Bignon, Yves-Jean YJ; , ; Rebbeck, Timothy R TR; Wagner, Theresa T; Lynch, Henry T HT; Domchek, Susan M SM; Nathanson, Katherine L KL; Garber, Judy E JE; Weitzel, Jeffrey J; Narod, Steven A SA; Tomlinson, Gail G; Olopade, Olufunmilayo I OI; Godwin, Andrew A; Isaacs, Claudine C; Jakubowska, Anna A; Lubinski, Jan J; Gronwald, Jacek J; Górski, Bohdan B; Byrski, Tomasz T; Huzarski, Tomasz T; Peock, Susan S; Cook, Margaret M; Baynes, Caroline C; Murray, Alexandra A; Rogers, Mark M; Daly, Peter A PA; Dorkins, Huw H; , ; Schmutzler, Rita K RK; Versmold, Beatrix B; Engel, Christoph C; Meindl, Alfons A; Arnold, Norbert N; Niederacher, Dieter D; Deissler, Helmut H; , ; Spurdle, Amanda B AB; Chen, Xiaoqing X; Waddell, Nicola N; Cloonan, Nicole N; , ; Kirchhoff, Tomas T; Offit, Kenneth K; Friedman, Eitan E; Kaufmann, Bella B; Laitman, Yael Y; Galore, Gilli G; Rennert, Gad G; Lejbkowicz, Flavio F; Raskin, Leon L; Andrulis, Irene L IL; Ilyushik, Eduard E; Ozcelik, Hilmi H; Devilee, Peter P; Vreeswijk, Maaike P G MP; Greene, Mark H MH; Prindiville, Sheila A SA; Osorio, Ana A; Benitez, Javier J; Zikan, Michal M; Szabo, Csilla I CI; Kilpivaara, Outi O; Nevanlinna, Heli H; Hamann, Ute U; Durocher, Francine F; Arason, Adalgeir A; Couch, Fergus J FJ; Easton, Douglas F DF; Chenevix-Trench, Georgia G; ,
Publication Date: 2007-12

Variant appearance in text: rs2304579
PubMed Link: 17999359
Variant Present in the following documents:
  • Main text
View BVdb publication page