BRCA1 c.4113G>A ;(p.G1371=)

Variant ID: 17-41243033-C-T

NM_007294.3(BRCA1):c.4113G>A;(p.G1371=)

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Familial history and prevalence of BRCA1, BRCA2 and TP53 pathogenic variants in HBOC Brazilian patients from a public healthcare service.

Scientific Reports
Matta, Bruna Palma BP; Gomes, Renan R; Mattos, Daniel D; Olicio, Renata R; Nascimento, Caroline Macedo CM; Ferreira, Gerson Moura GM; Brant, Ayslan Castro AC; Boroni, Mariana M; Furtado, Carolina C; Lima, Valdirene V; Moreira, Miguel Ângelo Martins MÂM; Dos Santos, Anna Cláudia Evangelista ACE
Publication Date: 2022-11-03

Variant appearance in text: N/A
PubMed Link: 36329109
Variant Present in the following documents:
View BVdb publication page



Germline and Somatic mutations in postmenopausal breast cancer patients.

Clinics (Sao Paulo, Brazil)
Nagy, Tauana Rodrigues TR; Maistro, Simone S; Encinas, Giselly G; Katayama, Maria Lucia Hirata MLH; Pereira, Glaucia Fernanda de Lima GFL; Gaburo-Júnior, Nelson N; Franco, Lucas Augusto Moyses LAM; Gouvêa, Ana Carolina Ribeiro Chaves de ACRC; Diz, Maria Del Pilar Estevez MDPE; Leite, Luiz Antonio Senna LAS; Folgueira, Maria Aparecida Azevedo Koike MAAK
Publication Date: 2021

Variant appearance in text: BRCA1: G1371=; rs147448807
PubMed Link: 34287479
Variant Present in the following documents:
  • Main text
  • cln-76-2837.pdf
View BVdb publication page



Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case-control study.

Bmc Cancer
Zayas-Villanueva, Omar Alejandro OA; Campos-Acevedo, Luis Daniel LD; Lugo-Trampe, José de Jesús JJ; Hernández-Barajas, David D; González-Guerrero, Juan Francisco JF; Noriega-Iriondo, María Fernanda MF; Ramírez-Sánchez, Ilse Alejandra IA; Martínez-de-Villarreal, Laura Elia LE
Publication Date: 2019-07-22

Variant appearance in text: BRCA1: Gly1371=; rs147448807
PubMed Link: 31331294
Variant Present in the following documents:
  • 12885_2019_5950_MOESM1_ESM.xlsx, sheet 3
View BVdb publication page



Sources of discordance among germ-line variant classifications in ClinVar.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S
Publication Date: 2017-10

Variant appearance in text: BRCA1: 4113G>A; Gly1371=
PubMed Link: 28569743
Variant Present in the following documents:
  • gim201760x7.xlsx, sheet 2
View BVdb publication page



Genetic testing in hereditary breast and ovarian cancer using massive parallel sequencing.

Biomed Research International
Ruiz, Anna A; Llort, Gemma G; Yagüe, Carmen C; Baena, Neus N; Viñas, Marina M; Torra, Montse M; Brunet, Anna A; Seguí, Miquel A MA; Saigí, Eugeni E; Guitart, Miriam M
Publication Date: 2014

Variant appearance in text: BRCA1: 4113G>A
PubMed Link: 25136594
Variant Present in the following documents:
  • 542541.f1.pdf
View BVdb publication page



BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families.

Disease Markers
Cherbal, Farid F; Salhi, Nadjet N; Bakour, Rabah R; Adane, Saida S; Boualga, Kada K; Maillet, Philippe P
Publication Date: 2012

Variant appearance in text: BRCA1: 4113G>A
PubMed Link: 22684231
Variant Present in the following documents:
  • DM32-06-234136.pdf
View BVdb publication page



BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families.

Disease Markers
Cherbal, Farid F; Bakour, Rabah R; Adane, Saida S; Boualga, Kada K; Benais-Pont, Gaelle G; Maillet, Philippe P
Publication Date: 2010

Variant appearance in text: BRCA1: 4113G>A
PubMed Link: 20683152
Variant Present in the following documents:
  • DM28-06-585278.pdf
View BVdb publication page