BRCA1 c.1115G>A ;(p.W372*)

Variant ID: 17-41246433-C-T

NM_007294.3(BRCA1):c.1115G>A;(p.W372*)

This variant was identified in 29 publications

View GRCh38 version.




Publications:


Whole-exome Sequencing of Nigerian Prostate Tumors from the Prostate Cancer Transatlantic Consortium (CaPTC) Reveals DNA Repair Genes Associated with African Ancestry.

Cancer Research Communications
White, Jason A JA; Kaninjing, Ernest T ET; Adeniji, Kayode A KA; Jibrin, Paul P; Obafunwa, John O JO; Ogo, Chidiebere N CN; Mohammed, Faruk F; Popoola, Ademola A; Fatiregun, Omolara A OA; Oluwole, Olabode P OP; Karanam, Balasubramanyam B; Elhussin, Isra I; Ambs, Stefan S; Tang, Wei W; Davis, Melissa M; Polak, Paz P; Campbell, Moray J MJ; Brignole, Kathryn R KR; Rotimi, Solomon O SO; Dean-Colomb, Windy W; Odedina, Folake T FT; Martin, Damali N DN; Yates, Clayton C
Publication Date: 2022-09

Variant appearance in text: BRCA1: 1115G>A; Trp372Ter; rs397508838
PubMed Link: 36922933
Variant Present in the following documents:
  • crc-22-0136-s01.xlsx, sheet 1
View BVdb publication page



Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: BRCA1: 1115G>A; Trp372Ter
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.

International Journal Of Cancer
Qin, Zixin Z; Li, Jiaheng J; Tam, Benjamin B; Sinha, Siddharth S; Zhao, Bojin B; Bhaskaran, Shanmuga Priya SP; Huang, Teng T; Wu, Xiaobing X; Chian, Jia Sheng JS; Guo, Maoni M; Kou, Si Hoi SH; Lei, Huijun H; Zhang, Li L; Wang, Xiaoyu X; Lagniton, Philip Naderev P PNP; Xiao, Fengxia F; Jiang, Xinyang X; Wang, San Ming SM
Publication Date: 2022-11-17

Variant appearance in text: BRCA1: 1115G>A; Trp372*; rs397508838
PubMed Link: 36385461
Variant Present in the following documents:
  • IJC-152-1159-s006.xlsx, sheet 2
  • IJC-152-1159-s011.xlsx, sheet 1
  • IJC-152-1159-s010.xlsx, sheet 4
  • IJC-152-1159-s009.xlsx, sheet 1
  • IJC-152-1159-s002.xlsx, sheet 1
  • IJC-152-1159-s005.xlsx, sheet 2
  • IJC-152-1159-s010.xlsx, sheet 1
View BVdb publication page



Analysis of matched primary and recurrent BRCA1/2 mutation-associated tumors identifies recurrence-specific drivers.

Nature Communications
Shah, Jennifer B JB; Pueschl, Dana D; Wubbenhorst, Bradley B; Fan, Mengyao M; Pluta, John J; D'Andrea, Kurt K; Hubert, Anna P AP; Shilan, Jake S JS; Zhou, Wenting W; Kraya, Adam A AA; Llop Guevara, Alba A; Ruan, Catherine C; Serra, Violeta V; Balmaña, Judith J; Feldman, Michael M; Morin, Pat J PJ; Nayak, Anupma A; Maxwell, Kara N KN; Domchek, Susan M SM; Nathanson, Katherine L KL
Publication Date: 2022-11-07

Variant appearance in text: BRCA1: W372X
PubMed Link: 36344544
Variant Present in the following documents:
  • 41467_2022_34523_MOESM14_ESM.xlsx, sheet 3
View BVdb publication page



Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.

Communications Biology
Hakkaart, Christopher C; Pearson, John F JF; Marquart, Louise L; Dennis, Joe J; Wiggins, George A R GAR; Barnes, Daniel R DR; Robinson, Bridget A BA; Mace, Peter D PD; Aittomäki, Kristiina K; Andrulis, Irene L IL; Arun, Banu K BK; Azzollini, Jacopo J; Balmaña, Judith J; Barkardottir, Rosa B RB; Belhadj, Sami S; Berger, Lieke L; Blok, Marinus J MJ; Boonen, Susanne E SE; Borde, Julika J; Bradbury, Angela R AR; Brunet, Joan J; Buys, Saundra S SS; Caligo, Maria A MA; Campbell, Ian I; Chung, Wendy K WK; Claes, Kathleen B M KBM; , ; , ; Collonge-Rame, Marie-Agnès MA; Cook, Jackie J; Cosgrove, Casey C; Couch, Fergus J FJ; Daly, Mary B MB; Dandiker, Sita S; Davidson, Rosemarie R; de la Hoya, Miguel M; de Putter, Robin R; Delnatte, Capucine C; Dhawan, Mallika M; Diez, Orland O; Ding, Yuan Chun YC; Domchek, Susan M SM; Donaldson, Alan A; Eason, Jacqueline J; Easton, Douglas F DF; Ehrencrona, Hans H; Engel, Christoph C; Evans, D Gareth DG; Faust, Ulrike U; Feliubadaló, Lidia L; Fostira, Florentia F; Friedman, Eitan E; Frone, Megan M; Frost, Debra D; Garber, Judy J; Gayther, Simon A SA; Gehrig, Andrea A; Gesta, Paul P; Godwin, Andrew K AK; Goldgar, David E DE; Greene, Mark H MH; Hahnen, Eric E; Hake, Christopher R CR; Hamann, Ute U; Hansen, Thomas V O TVO; Hauke, Jan J; Hentschel, Julia J; Herold, Natalie N; Honisch, Ellen E; Hulick, Peter J PJ; Imyanitov, Evgeny N EN; , ; , ; , ; Isaacs, Claudine C; Izatt, Louise L; Izquierdo, Angel A; Jakubowska, Anna A; James, Paul A PA; Janavicius, Ramunas R; John, Esther M EM; Joseph, Vijai V; Karlan, Beth Y BY; Kemp, Zoe Z; Kirk, Judy J; Konstantopoulou, Irene I; Koudijs, Marco M; Kwong, Ava A; Laitman, Yael Y; Lalloo, Fiona F; Lasset, Christine C; Lautrup, Charlotte C; Lazaro, Conxi C; Legrand, Clémentine C; Leslie, Goska G; Lesueur, Fabienne F; Mai, Phuong L PL; Manoukian, Siranoush S; Mari, Véronique V; Martens, John W M JWM; McGuffog, Lesley L; Mebirouk, Noura N; Meindl, Alfons A; Miller, Austin A; Montagna, Marco M; Moserle, Lidia L; Mouret-Fourme, Emmanuelle E; Musgrave, Hannah H; Nambot, Sophie S; Nathanson, Katherine L KL; Neuhausen, Susan L SL; Nevanlinna, Heli H; Yie, Joanne Ngeow Yuen JNY; Nguyen-Dumont, Tu T; Nikitina-Zake, Liene L; Offit, Kenneth K; Olah, Edith E; Olopade, Olufunmilayo I OI; Osorio, Ana A; Ott, Claus-Eric CE; Park, Sue K SK; Parsons, Michael T MT; Pedersen, Inge Sokilde IS; Peixoto, Ana A; Perez-Segura, Pedro P; Peterlongo, Paolo P; Pocza, Timea T; Radice, Paolo P; Ramser, Juliane J; Rantala, Johanna J; Rodriguez, Gustavo C GC; Rønlund, Karina K; Rosenberg, Efraim H EH; Rossing, Maria M; Schmutzler, Rita K RK; Shah, Payal D PD; Sharif, Saba S; Sharma, Priyanka P; Side, Lucy E LE; Simard, Jacques J; Singer, Christian F CF; Snape, Katie K; Steinemann, Doris D; Stoppa-Lyonnet, Dominique D; Sutter, Christian C; Tan, Yen Yen YY; Teixeira, Manuel R MR; Teo, Soo Hwang SH; Thomassen, Mads M; Thull, Darcy L DL; Tischkowitz, Marc M; Toland, Amanda E AE; Trainer, Alison H AH; Tripathi, Vishakha V; Tung, Nadine N; van Engelen, Klaartje K; van Rensburg, Elizabeth J EJ; Vega, Ana A; Viel, Alessandra A; Walker, Lisa L; Weitzel, Jeffrey N JN; Wevers, Marike R MR; Chenevix-Trench, Georgia G; Spurdle, Amanda B AB; Antoniou, Antonis C AC; Walker, Logan C LC
Publication Date: 2022-10-06

Variant appearance in text: BRCA1: 1115G>A; Trp372X
PubMed Link: 36203093
Variant Present in the following documents:
  • 42003_2022_3978_MOESM4_ESM.xlsx, sheet 14
View BVdb publication page



Clinical relevance of pathogenic germline variants in mismatch repair genes in Chinese breast cancer patients.

Npj Breast Cancer
Hu, Li L; Sun, Jie J; Li, Zhongwu Z; Qu, Ziwei Z; Liu, Yan Y; Wan, Qiting Q; Liu, Jiaming J; Ding, Xinyun X; Zang, Fan F; Zhang, Juan J; Yao, Lu L; Xu, Ye Y; Wang, Yin Y; Xie, Yuntao Y
Publication Date: 2022-04-21

Variant appearance in text: BRCA1: 1115G>A
PubMed Link: 35449176
Variant Present in the following documents:
  • 41523_2022_417_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil.

Breast Cancer Research And Treatment
Felix, Gabriela E S GES; Guindalini, Rodrigo Santa Cruz RSC; Zheng, Yonglan Y; Walsh, Tom T; Sveen, Elisabeth E; Lopes, Taisa Manuela Machado TMM; Côrtes, Juliana J; Zhang, Jing J; Carôzo, Polyanna P; Santos, Irlânia I; Bonfim, Thaís Ferreira TF; Garicochea, Bernardo B; Toralles, Maria Betânia Pereira MBP; Meyer, Roberto R; Netto, Eduardo Martins EM; Abe-Sandes, Kiyoko K; King, Mary-Claire MC; de Oliveira Nascimento, Ivana Lucia IL; Olopade, Olufunmilayo I OI
Publication Date: 2022-06

Variant appearance in text: BRCA1: 1115G>A
PubMed Link: 35353237
Variant Present in the following documents:
  • Main text
  • 10549_2022_Article_6560.pdf
View BVdb publication page



Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.

Haematologica
Gilad, Oded O; Dgany, Orly O; Noy-Lotan, Sharon S; Krasnov, Tanya T; Yacobovich, Joanne J; Rabinowicz, Ron R; Goldberg, Tracie T; Kuperman, Amir A AA; Abu-Quider, Abed A; Miskin, Hagit H; Kapelushnik, Noa N; Mandel-Shorer, Noa N; Shimony, Shai S; Harlev, Dan D; Ben-Ami, Tal T; Adam, Etai E; Levin, Carina C; Aviner, Shraga S; Elhasid, Ronit R; Berger-Achituv, Sivan S; Chaitman-Yerushalmi, Lilach L; Kodman, Yona Y; Oniashvilli, Nino N; Hameiri-Grosman, Michal M; Izraeli, Shai S; Tamary, Hannah H; Steinberg-Shemer, Orna O
Publication Date: 2022-09-01

Variant appearance in text: BRCA1: 1115G>A; Trp372Ter; rs397508838
PubMed Link: 35295078
Variant Present in the following documents:
  • 2021_280116_GILAD_SUPPL.pdf
  • 1072081.pdf
View BVdb publication page



Human BRCA pathogenic variants were originated during recent human history.

Life Science Alliance
Li, Jiaheng J; Zhao, Bojin B; Huang, Teng T; Qin, Zixin Z; Wang, San Ming SM
Publication Date: 2022-05

Variant appearance in text: BRCA1: W372X
PubMed Link: 35165121
Variant Present in the following documents:
  • LSA-2021-01263_TableS5.xlsx, sheet 2
View BVdb publication page



A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: BRCA1: W372*; rs397508838
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 7
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 4
View BVdb publication page



The shifting landscape of genetic alterations separating endometriosis and ovarian endometrioid carcinoma.

American Journal Of Cancer Research
Gaia-Oltean, Adriana I AI; Pop, Laura A LA; Cojocneanu, Roxana M RM; Buse, Mihail M; Zimta, Andreea A AA; Kubelac, Paul P; Irimie, Alexandru A; Coza, Ovidiu F OF; Roman, Horace H; Berindan-Neagoe, Ioana I
Publication Date: 2021

Variant appearance in text: BRCA1: 1115G>A
PubMed Link: 33948387
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of pathogenic variants in cancer genes using base editing screens with editing efficiency correction.

Genome Biology
Huang, Changcai C; Li, Guangyu G; Wu, Jiayu J; Liang, Junbo J; Wang, Xiaoyue X
Publication Date: 2021-03-10

Variant appearance in text: BRCA1: W372X
PubMed Link: 33691754
Variant Present in the following documents:
  • 13059_2021_2305_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Germline molecular data in hereditary breast cancer in Brazil: Lessons from a large single-center analysis.

Plos One
Sandoval, Renata Lazari RL; Leite, Ana Carolina Rathsam ACR; Barbalho, Daniel Meirelles DM; Assad, Daniele Xavier DX; Barroso, Romualdo R; Polidorio, Natalia N; Dos Anjos, Carlos Henrique CH; de Miranda, Andréa Discaciati AD; Ferreira, Ana Carolina Salles de Mendonça ACSM; Fernandes, Gustavo Dos Santos GDS; Achatz, Maria Isabel MI
Publication Date: 2021

Variant appearance in text: BRCA1: 1115G>A; Trp372*; rs397508838
PubMed Link: 33606809
Variant Present in the following documents:
  • Main text
  • pone.0247363.pdf
View BVdb publication page



A Case Report of Germline Compound Heterozygous Mutations in the BRCA1 Gene of an Ovarian and Breast Cancer Patient.

International Journal Of Molecular Sciences
Kwong, Ava A; Ho, Cecilia Y S CYS; Shin, Vivian Y VY; Au, Chun Hang CH; Chan, Tsun Leung TL; Ma, Edmond S K ESK
Publication Date: 2021-01-17

Variant appearance in text: BRCA1: Trp372*
PubMed Link: 33477375
Variant Present in the following documents:
  • Main text
  • ijms-22-00889.pdf
View BVdb publication page



Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency.

Journal Of Medical Genetics
Chirita-Emandi, Adela A; Andreescu, Nicoleta N; Popa, Cristina C; Mihailescu, Alexandra A; Riza, Anca-Lelia AL; Plesea, Razvan R; Ioana, Mihai M; Arghirescu, Smaranda S; Puiu, Maria M
Publication Date: 2021-09

Variant appearance in text: BRCA1: 1115G>A; Trp372Ter
PubMed Link: 32843487
Variant Present in the following documents:
  • Main text
  • jmedgenet-2020-107198.pdf
View BVdb publication page



Prediction of the functional impact of missense variants in BRCA1 and BRCA2 with BRCA-ML.

Npj Breast Cancer
Hart, Steven N SN; Polley, Eric C EC; Shimelis, Hermella H; Yadav, Siddhartha S; Couch, Fergus J FJ
Publication Date: 2020

Variant appearance in text: BRCA1: 1115G>A; Trp372X
PubMed Link: 32377563
Variant Present in the following documents:
  • 41523_2020_159_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes.

Scientific Reports
De Talhouet, Solene S; Peron, Julien J; Vuilleumier, Aurelie A; Friedlaender, Alex A; Viassolo, Valeria V; Ayme, Aurélie A; Bodmer, Alexandre A; Treilleux, Isabelle I; Lang, Noemie N; Tille, Jean- Christophe JC; Chappuis, Pierre O PO; Buisson, Adrien A; Giraud, Sophie S; Lasset, Christine C; Bonadona, Valerie V; Trédan, Olivier O; Labidi-Galy, S Intidhar SI
Publication Date: 2020-04-27

Variant appearance in text: BRCA1: 1115G>A; Trp372*
PubMed Link: 32341426
Variant Present in the following documents:
  • 41598_2020_63759_MOESM1_ESM.pdf
View BVdb publication page



OncoOmics approaches to reveal essential genes in breast cancer: a panoramic view from pathogenesis to precision medicine.

Scientific Reports
López-Cortés, Andrés A; Paz-Y-Miño, César C; Guerrero, Santiago S; Cabrera-Andrade, Alejandro A; Barigye, Stephen J SJ; Munteanu, Cristian R CR; González-Díaz, Humberto H; Pazos, Alejandro A; Pérez-Castillo, Yunierkis Y; Tejera, Eduardo E
Publication Date: 2020-03-24

Variant appearance in text: N/A
PubMed Link: 32210335
Variant Present in the following documents:
View BVdb publication page



Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Li, Hongyan H; LaDuca, Holly H; Pesaran, Tina T; Chao, Elizabeth C EC; Dolinsky, Jill S JS; Parsons, Michael M; Spurdle, Amanda B AB; Polley, Eric C EC; Shimelis, Hermela H; Hart, Steven N SN; Hu, Chunling C; Couch, Fergus J FJ; Goldgar, David E DE
Publication Date: 2020-04

Variant appearance in text: BRCA1: 1115G>A
PubMed Link: 31853058
Variant Present in the following documents:
  • 41436_2019_729_MOESM2_ESM.xls, sheet 1
View BVdb publication page



Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility.

Molecular Genetics & Genomic Medicine
Keupp, Katharina K; Hampp, Stephanie S; Hübbel, Annette A; Maringa, Monika M; Kostezka, Sarah S; Rhiem, Kerstin K; Waha, Anke A; Wappenschmidt, Barbara B; Pujol, Roser R; Surrallés, Jordi J; Schmutzler, Rita K RK; Wiesmüller, Lisa L; Hahnen, Eric E
Publication Date: 2019-09

Variant appearance in text: BRCA1: Trp372*
PubMed Link: 31347298
Variant Present in the following documents:
  • Main text
  • MGG3-7-e863.pdf
View BVdb publication page



Whole-exome sequencing of ovarian cancer families uncovers putative predisposition genes.

International Journal Of Cancer
Zhu, Qianqian Q; Zhang, Jianmin J; Chen, Yanmin Y; Hu, Qiang Q; Shen, He H; Huang, Ruea-Yea RY; Liu, Qian Q; Kaur, Jasmine J; Long, Mark M; Battaglia, Sebastiano S; Eng, Kevin H KH; Lele, Shashikant B SB; Zsiros, Emese E; Villella, Jeannine J; Lugade, Amit A; Yao, Song S; Liu, Song S; Moysich, Kirsten K; Odunsi, Kunle O KO
Publication Date: 2020-04-15

Variant appearance in text: BRCA1: W372X; rs397508838
PubMed Link: 31265121
Variant Present in the following documents:
View BVdb publication page



The germline mutational landscape of BRCA1 and BRCA2 in Brazil.

Scientific Reports
Palmero, Edenir Inêz EI; Carraro, Dirce Maria DM; Alemar, Barbara B; Moreira, Miguel Angelo Martins MAM; Ribeiro-Dos-Santos, Ândrea Â; Abe-Sandes, Kiyoko K; Galvão, Henrique Campos Reis HCR; Reis, Rui Manuel RM; de Pádua Souza, Cristiano C; Campacci, Natalia N; Achatz, Maria Isabel MI; Brianese, Rafael Canfield RC; da Cruz Formiga, Maria Nirvana MN; Makdissi, Fabiana Baroni FB; Vargas, Fernando Regla FR; Evangelista Dos Santos, Anna Cláudia AC; Seuanez, Hector N HN; Lobo de Souza, Kelly Rose KR; Netto, Cristina B O CBO; Santos-Silva, Patrícia P; da Silva, Gustavo Stumpf GS; Burbano, Rommel M R RMR; Santos, Sidney S; Assumpção, Paulo Pimentel PP; Bernardes, Izabel Maria Monteiro IMM; Machado-Lopes, Taisa Manuela Bonfim TMB; Bomfim, Thais Ferreira TF; Toralles, Maria Betânia Pereira MBP; Nascimento, Ivana I; Garicochea, Bernardo B; Simon, Sergio D SD; Noronha, Simone S; de Lima, Fernanda Teresa FT; Chami, Anisse Marques AM; Bittar, Camila Matzenbacher CM; Bines, Jose J; Artigalas, Osvaldo O; Esteves-Diz, Maria Del Pilar MDP; Lajus, Tirzah Braz Petta TBP; Gifoni, Ana Carolina Leite Vieira Costa ACLVC; Guindalini, Rodrigo S C RSC; Cintra, Terezinha Sarquis TS; Schwartz, Ida V D IVD; Bernardi, Pricila P; Miguel, Diego D; Nogueira, Sonia Tereza Dos Santos STDS; Herzog, Josef J; Weitzel, Jeffrey N JN; Ashton-Prolla, Patricia P
Publication Date: 2018-06-15

Variant appearance in text: BRCA1: 1115G>A
PubMed Link: 29907814
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_27315.pdf
  • 41598_2018_27315_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Seo, Aaron A; Steinberg-Shemer, Orna O; Unal, Sule S; Casadei, Silvia S; Walsh, Tom T; Gumruk, Fatma F; Shalev, Stavit S; Shimamura, Akiko A; Akarsu, Nurten Ayse NA; Tamary, Hannah H; King, Mary-Claire MC
Publication Date: 2018-05-15

Variant appearance in text: BRCA1: 1115G>A; W372X
PubMed Link: 29712865
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pathogenic Germline Variants in 10,389 Adult Cancers.

Cell
Huang, Kuan-Lin KL; Mashl, R Jay RJ; Wu, Yige Y; Ritter, Deborah I DI; Wang, Jiayin J; Oh, Clara C; Paczkowska, Marta M; Reynolds, Sheila S; Wyczalkowski, Matthew A MA; Oak, Ninad N; Scott, Adam D AD; Krassowski, Michal M; Cherniack, Andrew D AD; Houlahan, Kathleen E KE; Jayasinghe, Reyka R; Wang, Liang-Bo LB; Zhou, Daniel Cui DC; Liu, Di D; Cao, Song S; Kim, Young Won YW; Koire, Amanda A; McMichael, Joshua F JF; Hucthagowder, Vishwanathan V; Kim, Tae-Beom TB; Hahn, Abigail A; Wang, Chen C; McLellan, Michael D MD; Al-Mulla, Fahd F; Johnson, Kimberly J KJ; , ; Lichtarge, Olivier O; Boutros, Paul C PC; Raphael, Benjamin B; Lazar, Alexander J AJ; Zhang, Wei W; Wendl, Michael C MC; Govindan, Ramaswamy R; Jain, Sanjay S; Wheeler, David D; Kulkarni, Shashikant S; Dipersio, John F JF; Reimand, Jüri J; Meric-Bernstam, Funda F; Chen, Ken K; Shmulevich, Ilya I; Plon, Sharon E SE; Chen, Feng F; Ding, Li L
Publication Date: 2018-04-05

Variant appearance in text: BRCA1: W372*
PubMed Link: 29625052
Variant Present in the following documents:
  • Main text
View BVdb publication page



Combined Inhibition of ATR and WEE1 as a Novel Therapeutic Strategy in Triple-Negative Breast Cancer.

Neoplasia (New York, N.Y.)
Jin, Juan J; Fang, Hehui H; Yang, Fang F; Ji, Wenfei W; Guan, Nan N; Sun, Zijia Z; Shi, Yaqin Y; Zhou, Guohua G; Guan, Xiaoxiang X
Publication Date: 2018-05

Variant appearance in text: BRCA1: Trp372X
PubMed Link: 29605721
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genomic characteristics of trastuzumab-resistant Her2-positive metastatic breast cancer.

Journal Of Cancer Research And Clinical Oncology
de Oliveira Taveira, Mateus M; Nabavi, Sheida S; Wang, Yuker Y; Tonellato, Peter P; Esteva, Francisco J FJ; Cantley, Lewis C LC; Wulf, Gerburg M GM
Publication Date: 2017-07

Variant appearance in text: BRCA1: W372X
PubMed Link: 28247034
Variant Present in the following documents:
  • Main text
  • 432_2017_Article_2358.pdf
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: BRCA1: W372X
PubMed Link: 23318652
Variant Present in the following documents:
  • Main text
  • je-23-075-s001.pdf
  • je-23-075.pdf
View BVdb publication page



Characteristics of triple-negative breast cancer in patients with a BRCA1 mutation: results from a population-based study of young women.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Lee, Eunjung E; McKean-Cowdin, Roberta R; Ma, Huiyan H; Spicer, Darcy V DV; Van Den Berg, David D; Bernstein, Leslie L; Ursin, Giske G
Publication Date: 2011-11-20

Variant appearance in text: N/A
PubMed Link: 22010008
Variant Present in the following documents:
View BVdb publication page



Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: results from a population-based study of young breast cancer patients.

Breast Cancer Research : Bcr
Lee, Eunjung E; McKean-Cowdin, Roberta R; Ma, Huiyan H; Chen, Zhengjia Z; Van Den Berg, David D; Henderson, Brian E BE; Bernstein, Leslie L; Ursin, Giske G
Publication Date: 2008

Variant appearance in text: BRCA1: W372X
PubMed Link: 18284688
Variant Present in the following documents:
View BVdb publication page