BRCA2 c.1906_1907delinsAG ;(p.S636R)

Variant ID: 13-32907521-TC-AG

NM_000059.3(BRCA2):c.1906_1907delinsAG;(p.S636R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.

Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
Publication Date: 2018-12-13

Variant appearance in text: BRCA2: S636R
PubMed Link: 30545397
Variant Present in the following documents:
  • 13045_2018_679_MOESM3_ESM.pdf
View BVdb publication page