Variant #0000243963 (NC_000021.8:g.27264108C>T, NM_000484.3:c.2137G>A (APP))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27264108C>T
DNA change (hg38) g.25891796C>T
Published as -
ISCN -
DB-ID APP_000019 See all 6 reported entries
Variant remarks Detected in 1 AD patient and in 5 unaffected, aged relatives.. /r/Double point mutation in coding region. The first mutation at codon A713 causes an amino acid change. The second mutation at codon V715 is a silent mutation
Reference -
ClinVar ID -
dbSNP ID rs63750066
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0001 View details
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +02:00 (CEST)
Date last edited 2020-07-16 21:58:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APP NM_000484.3 +/? 17 c.2137G>A r.(?) p.(Ala713Thr)


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