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APP c.685G>A ;(p.A229T)
Variant ID: 21-27394336-C-T
NM_000484.3(
APP
):c.685G>A;(p.A229T)
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:
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.
Human Genetics
Cooper, David N DN; Krawczak, Michael M; Polychronakos, Constantin C; Tyler-Smith, Chris C; Kehrer-Sawatzki, Hildegard H
Publication Date: 2013-10
Variant appearance in text: APP: 685G>A; Ala229Thr
PubMed Link:
23820649
Variant Present in the following documents:
Main text
View BVdb publication page