APP c.626G>A ;(p.W209*)

Variant ID: 21-27423352-C-T

NM_000484.3(APP):c.626G>A;(p.W209*)

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:

Mutational analysis in familial Alzheimer's disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146Ile.

Scientific Reports
Lin, Yung-Shuan YS; Cheng, Chih-Ya CY; Liao, Yi-Chu YC; Hong, Chen-Jee CJ; Fuh, Jong-Ling JL
Publication Date: 2020-11-13

Variant appearance in text: APP: 626G>A
PubMed Link: 33188256
Variant Present in the following documents:
  • 41598_2020_76794_MOESM2_ESM.pdf
View BVdb publication page