APC c.3199_3200delinsAC ;(p.Q1067T)

Variant ID: 5-112174490-CA-AC

NM_000038.5(APC):c.3199_3200delinsAC;(p.Q1067T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition.

Plos One
Martin-Morales, Lorena L; Rofes, Paula P; Diaz-Rubio, Eduardo E; Llovet, Patricia P; Lorca, Victor V; Bando, Inmaculada I; Perez-Segura, Pedro P; de la Hoya, Miguel M; Garre, Pilar P; Garcia-Barberan, Vanesa V; Caldes, Trinidad T
Publication Date: 2018

Variant appearance in text: APC: Q1067T
PubMed Link: 30256826
Variant Present in the following documents:
  • Main text
  • pone.0203885.pdf
View BVdb publication page