BRCA2 c.1633_1635delinsATG ;(p.V545M)

Variant ID: 13-32907248-GTT-ATG

NM_000059.3(BRCA2):c.1633_1635delinsATG;(p.V545M)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31

Variant appearance in text: BRCA2: V545M
PubMed Link: 33384420
Variant Present in the following documents:
  • Main text
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