Variant #0000001542 (NC_000004.11:g.178355542dup, NM_000027.3:c.800dup (AGA))

Chromosome 4
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.178355542dup
DNA change (hg38) g.177434388dup
Published as ins T after T800
ISCN -
DB-ID AGA_000024
Variant remarks 1 Spanish-American AGU patient
Reference PubMed: Ikonen et al. 1991
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-08-30 14:17:27 +02:00 (CEST)
Date last edited 2019-02-27 20:52:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGA NM_000027.3 +/+ 7 c.800dup r.800dupu p.Pro268Alafs*52


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