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