BRCA2 c.1553_1554insT ;(p.S519Kfs*8)

Variant ID: 13-32907168-C-CT

NM_000059.3(BRCA2):c.1553_1554insT;(p.S519Kfs*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Improved Efficiency and Reliability of NGS Amplicon Sequencing Data Analysis for Genetic Diagnostic Procedures Using AGSA Software.

Biomed Research International
Poulet, Axel A; Privat, Maud M; Ponelle, Flora F; Viala, Sandrine S; Decousus, Stephanie S; Perin, Axel A; Lafarge, Laurence L; Ollier, Marie M; El Saghir, Nagi S NS; Uhrhammer, Nancy N; Bignon, Yves-Jean YJ; Bidet, Yannick Y
Publication Date: 2016

Variant appearance in text: BRCA2: 1553_1554insT
PubMed Link: 27656653
Variant Present in the following documents:
  • Main text
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