Variant #0000244044 (NC_000021.8:g.26185992G>A, NM_000484.3:c.(2124C>T) (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.26185992G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID APP_000021 See all 4 reported entries
Variant remarks Silent point mutation in coding region
Variant Error [EREF/EUNCERTAIN]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APP NM_000484.3 -/? 17 c.(2124C>T) r.(?) p.(=)


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