Variant #0000243967 (NC_000021.8:g.27269954C>G, NM_000484.3:c.1995G>C (APP))

Chromosome 21
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27269954C>G
DNA change (hg38) g.25897642C>G
Published as -
ISCN -
DB-ID APP_000022
Variant remarks Not segregating with disease. Detected in 1 patient and 1 unaffected, aged, relative.. /r/Point mutation in coding region predicting an amino acid substitution
Reference -
ClinVar ID -
dbSNP ID rs63750363
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 21:58:31 +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 -/? 16 c.1995G>C r.(?) p.(Glu665Asp)


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