APC c.2195dup ;(p.N732Kfs*2)

Variant ID: 5-112173483-C-CA

NM_000038.5(APC):c.2195dup;(p.N732Kfs*2)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comprehensive analysis of germline mutations in northern Brazil: a panel of 16 genes for hereditary cancer-predisposing syndrome investigation.

Bmc Cancer
Vidal, Amanda Ferreira AF; Ferraz, Rafaella Sousa RS; El-Husny, Antonette A; Silva, Caio Santos CS; Vinasco-Sandoval, Tatiana T; Magalhães, Leandro L; Raiol-Moraes, Milene M; Barra, Williams Fernandes WF; Pereira, Cynthia Lara Brito Lins CLBL; de Assumpção, Paulo Pimentel PP; de Brito, Leonardo Miranda LM; Vialle, Ricardo Assunção RA; Santos, Sidney S; Ribeiro-Dos-Santos, Ândrea Â; Ribeiro-Dos-Santos, André M AM
Publication Date: 2021-04-07

Variant appearance in text: APC: 2195dupA; Asn732fs
PubMed Link: 33827469
Variant Present in the following documents:
  • Main text
  • 12885_2021_Article_8089.pdf
View BVdb publication page