APC c.1204_1206delinsTGG ;(p.R402W)

Variant ID: 5-112154933-CGT-TGG

NM_000038.5(APC):c.1204_1206delinsTGG;(p.R402W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing.

Frontiers In Cardiovascular Medicine
Zhou, Yue Y; Bai, Kai K; Wang, Yu Y; Meng, Zhuo Z; Zhou, Shuang S; Jiang, Shiwei S; Wang, Hualin H; Wang, Jian J; Yang, Mei M; Wang, Qingjie Q; Sun, Kun K; Chen, Sun S
Publication Date: 2021

Variant appearance in text: APC: R402W
PubMed Link: 35141295
Variant Present in the following documents:
  • Main text
  • fcvm-08-811156.pdf
View BVdb publication page