APP c.1195G>A ;(p.E399K)

Variant ID: 21-27354686-C-T

NM_000484.3(APP):c.1195G>A;(p.E399K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease.

Faseb Journal : Official Publication Of The Federation Of American Societies For Experimental Biology
Westerlund, Marie M; Behbahani, Homira H; Gellhaar, Sandra S; Forsell, Charlotte C; Belin, Andrea Carmine AC; Anvret, Anna A; Zettergren, Anna A; Nissbrandt, Hans H; Lind, Charlotta C; Sydow, Olof O; Graff, Caroline C; Olson, Lars L; Ankarcrona, Maria M; Galter, Dagmar D
Publication Date: 2011-04

Variant appearance in text: APP: 1195G>A
PubMed Link: 21163861
Variant Present in the following documents:
  • Main text
View BVdb publication page