BRCA1 c.4699G>T ;(p.G1567*)

Variant ID: 17-41223232-C-A

NM_007294.3(BRCA1):c.4699G>T;(p.G1567*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: 4699G>T; Gly1567X
PubMed Link: 32377563
Variant Present in the following documents:
  • 41523_2020_159_MOESM3_ESM.xlsx, sheet 1
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Clinical and molecular characterization of patients with cancer of unknown primary in the modern era.

Annals Of Oncology : Official Journal Of The European Society For Medical Oncology
Varghese, A M AM; Arora, A A; Capanu, M M; Camacho, N N; Won, H H HH; Zehir, A A; Gao, J J; Chakravarty, D D; Schultz, N N; Klimstra, D S DS; Ladanyi, M M; Hyman, D M DM; Solit, D B DB; Berger, M F MF; Saltz, L B LB
Publication Date: 2017-12-01

Variant appearance in text: BRCA1: G1567*
PubMed Link: 29045506
Variant Present in the following documents:
  • Main text
View BVdb publication page