APC c.556_558delinsTGT ;(p.R186C)

Variant ID: 5-112116511-AGA-TGT

NM_000038.5(APC):c.556_558delinsTGT;(p.R186C)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Analysis of genetic alterations identifies the frequent mutation of GNAS in colorectal laterally spreading tumors.

Cancer Communications (London, England)
Nong, Yanying Y; Zhang, Yuru Y; Zhang, Yi Y; Pan, Lei L; Chen, Junsheng J; Zhu, Chaojun C; Han, Lu L; Li, Aimin A; Liu, Side S
Publication Date: 2020-11

Variant appearance in text: APC: R186C
PubMed Link: 32762003
Variant Present in the following documents:
  • Main text
View BVdb publication page



The biological basis and function of GNAS mutation in pseudomyxoma peritonei: a review.

Journal Of Cancer Research And Clinical Oncology
Lin, Yu-Lin YL; Ma, Ru R; Li, Yan Y
Publication Date: 2020-09

Variant appearance in text: APC: R186C
PubMed Link: 32700107
Variant Present in the following documents:
  • Main text
  • 432_2020_Article_3321.pdf
View BVdb publication page



Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material.

Plos One
de Leng, Wendy W J WW; Gadellaa-van Hooijdonk, Christa G CG; Barendregt-Smouter, Françoise A S FA; Koudijs, Marco J MJ; Nijman, Ies I; Hinrichs, John W J JW; Cuppen, Edwin E; van Lieshout, Stef S; Loberg, Robert D RD; de Jonge, Maja M; Voest, Emile E EE; de Weger, Roel A RA; Steeghs, Neeltje N; Langenberg, Marlies H G MH; Sleijfer, Stefan S; Willems, Stefan M SM; Lolkema, Martijn P MP
Publication Date: 2016

Variant appearance in text: APC: R186C
PubMed Link: 26919633
Variant Present in the following documents:
  • pone.0149405.s010.xlsx, sheet 1
View BVdb publication page