Bibliome.ai browser hg19
Search
About
Stats
FAQ
APC c.1431A>T ;(p.E477D)
Variant ID: 5-112162827-A-T
NM_000038.5(
APC
):c.1431A>T;(p.E477D)
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:
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Respiratory Research
Wang, Mingbang M; Zhuang, Deyi D; Mei, Mei M; Ma, Haiyan H; Li, Zixiu Z; He, Fusheng F; Cheng, Guoqiang G; Lin, Guang G; Zhou, Wenhao W
Publication Date: 2020-02-13
Variant appearance in text: APC: E477D
PubMed Link:
32054482
Variant Present in the following documents:
Main text
12931_2020_Article_1314.pdf
View BVdb publication page