APP c.1978A>T ;(p.N660Y)

Variant ID: 21-27269971-T-A

NM_000484.3(APP):c.1978A>T;(p.N660Y)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Genomics and Functional Genomics of Alzheimer's Disease.

Neurotherapeutics : The Journal Of The American Society For Experimental Neurotherapeutics
Kamboh, M Ilyas MI
Publication Date: 2022-01

Variant appearance in text: APP: Asn660Tyr
PubMed Link: 34935119
Variant Present in the following documents:
  • Main text
  • 13311_2021_Article_1152.pdf
View BVdb publication page



Processing of Mutant β-Amyloid Precursor Protein and the Clinicopathological Features of Familial Alzheimer's Disease.

Aging And Disease
Bi, Christopher C; Bi, Stephanie S; Li, Bin B
Publication Date: 2019-04

Variant appearance in text: APP: N660Y
PubMed Link: 31011484
Variant Present in the following documents:
  • Main text
  • ad-10-2-383.pdf
View BVdb publication page



Monoaminergic neuropathology in Alzheimer's disease.

Progress In Neurobiology
Šimić, Goran G; Babić Leko, Mirjana M; Wray, Selina S; Harrington, Charles R CR; Delalle, Ivana I; Jovanov-Milošević, Nataša N; Bažadona, Danira D; Buée, Luc L; de Silva, Rohan R; Di Giovanni, Giuseppe G; Wischik, Claude M CM; Hof, Patrick R PR
Publication Date: 2017-04

Variant appearance in text: APP: Asn660Tyr
PubMed Link: 27084356
Variant Present in the following documents:
  • Main text
View BVdb publication page



Rare Variants and Transcriptomics in Alzheimer disease.

Current Genetic Medicine Reports
Humphries, Crystal C; Kohli, Martin A MA
Publication Date: 2014-06-01

Variant appearance in text: APP: N660Y
PubMed Link: 25045597
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alzheimer's disease risk genes and mechanisms of disease pathogenesis.

Biological Psychiatry
Karch, Celeste M CM; Goate, Alison M AM
Publication Date: 2015-01-01

Variant appearance in text: APP: N660Y
PubMed Link: 24951455
Variant Present in the following documents:
  • Main text
View BVdb publication page



Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.

Plos One
Cruchaga, Carlos C; Haller, Gabe G; Chakraverty, Sumitra S; Mayo, Kevin K; Vallania, Francesco L M FL; Mitra, Robi D RD; Faber, Kelley K; Williamson, Jennifer J; Bird, Tom T; Diaz-Arrastia, Ramon R; Foroud, Tatiana M TM; Boeve, Bradley F BF; Graff-Radford, Neill R NR; St Jean, Pamela P; Lawson, Michael M; Ehm, Margaret G MG; Mayeux, Richard R; Goate, Alison M AM; ,
Publication Date: 2012

Variant appearance in text: APP: N660Y
PubMed Link: 22312439
Variant Present in the following documents:
  • Main text
  • pone.0031039.pdf
View BVdb publication page