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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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