APP c.410A>G ;(p.H137R)

Variant ID: 21-27425610-T-C

NM_000484.3(APP):c.410A>G;(p.H137R)

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:

Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers.

Human Mutation
Lalli, Matthew A MA; Garcia, Gloria G; Madrigal, Lucia L; Arcos-Burgos, Mauricio M; Arcila, Mary Luz ML; Kosik, Kenneth S KS; Lopera, Francisco F
Publication Date: 2012-12

Variant appearance in text: APP: 410A>G; His137Arg
PubMed Link: 22829467
Variant Present in the following documents:
  • Main text
View BVdb publication page