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APP c.88G>A ;(p.A30T)
Variant ID: 21-27484433-C-T
NM_000484.3(
APP
):c.88G>A;(p.A30T)
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:
Visualizing APP and BACE-1 approximation in neurons yields insight into the amyloidogenic pathway.
Nature Neuroscience
Das, Utpal U; Wang, Lina L; Ganguly, Archan A; Saikia, Junmi M JM; Wagner, Steven L SL; Koo, Edward H EH; Roy, Subhojit S
Publication Date: 2016-01
Variant appearance in text: APP: A30T
PubMed Link:
26642089
Variant Present in the following documents:
Main text
nihms736516.pdf
View BVdb publication page