BRCA2 c.1437C>G ;(p.D479E)

Variant ID: 13-32907052-C-G

NM_000059.3(BRCA2):c.1437C>G;(p.D479E)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Understanding and predicting the functional consequences of missense mutations in BRCA1 and BRCA2.

Scientific Reports
Aljarf, Raghad R; Shen, Mengyuan M; Pires, Douglas E V DEV; Ascher, David B DB
Publication Date: 2022-06-21

Variant appearance in text: BRCA2: D479E
PubMed Link: 35729312
Variant Present in the following documents:
  • 41598_2022_13508_MOESM2_ESM.xlsx, sheet 1
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: BRCA2: 1437C>G; Asp479Glu
PubMed Link: 32377563
Variant Present in the following documents:
  • 41523_2020_159_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Pancreatic acinar cell carcinoma is associated with BRCA2 germline mutations: a case report and literature review.

Cancer Biology & Therapy
Kryklyva, Valentyna V; Haj Mohammad, Nadia N; Morsink, Folkert H M FHM; Ligtenberg, Marjolijn J L MJL; Offerhaus, G Johan A GJA; Nagtegaal, Iris D ID; de Leng, Wendy W J WWJ; Brosens, Lodewijk A A LAA
Publication Date: 2019

Variant appearance in text: BRCA2: 1437C>G; D479E
PubMed Link: 31002019
Variant Present in the following documents:
  • Main text
  • kcbt-20-07-1595274.pdf
View BVdb publication page



Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Hart, Steven N SN; Hoskin, Tanya T; Shimelis, Hermela H; Moore, Raymond M RM; Feng, Bingjian B; Thomas, Abigail A; Lindor, Noralane M NM; Polley, Eric C EC; Goldgar, David E DE; Iversen, Edwin E; Monteiro, Alvaro N A ANA; Suman, Vera J VJ; Couch, Fergus J FJ
Publication Date: 2019-01

Variant appearance in text: BRCA2: D479E
PubMed Link: 29884841
Variant Present in the following documents:
  • NIHMS953431-supplement-Table_S2.xls, sheet 1
View BVdb publication page



Mutations driving CLL and their evolution in progression and relapse.

Nature
Landau, Dan A DA; Tausch, Eugen E; Taylor-Weiner, Amaro N AN; Stewart, Chip C; Reiter, Johannes G JG; Bahlo, Jasmin J; Kluth, Sandra S; Bozic, Ivana I; Lawrence, Mike M; Böttcher, Sebastian S; Carter, Scott L SL; Cibulskis, Kristian K; Mertens, Daniel D; Sougnez, Carrie L CL; Rosenberg, Mara M; Hess, Julian M JM; Edelmann, Jennifer J; Kless, Sabrina S; Kneba, Michael M; Ritgen, Matthias M; Fink, Anna A; Fischer, Kirsten K; Gabriel, Stacey S; Lander, Eric S ES; Nowak, Martin A MA; Döhner, Hartmut H; Hallek, Michael M; Neuberg, Donna D; Getz, Gad G; Stilgenbauer, Stephan S; Wu, Catherine J CJ
Publication Date: 2015-10-22

Variant appearance in text: BRCA2: 1437C>G; D479E
PubMed Link: 26466571
Variant Present in the following documents:
  • NIHMS715090-supplement-Supplementary_Table_3.xlsx, sheet 1
View BVdb publication page



Whole exome sequencing reveals recurrent mutations in BRCA2 and FAT genes in acinar cell carcinomas of the pancreas.

Scientific Reports
Furukawa, Toru T; Sakamoto, Hitomi H; Takeuchi, Shoko S; Ameri, Mitra M; Kuboki, Yuko Y; Yamamoto, Toshiyuki T; Hatori, Takashi T; Yamamoto, Masakazu M; Sugiyama, Masanori M; Ohike, Nobuyuki N; Yamaguchi, Hiroshi H; Shimizu, Michio M; Shibata, Noriyuki N; Shimizu, Kyoko K; Shiratori, Keiko K
Publication Date: 2015-03-06

Variant appearance in text: BRCA2: D479E
PubMed Link: 25743105
Variant Present in the following documents:
  • Main text
  • srep08829.pdf
View BVdb publication page