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