Variant #0000001532 (NC_000004.11:g.178360754_178360757del, NM_000027.3:c.373_376del (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.178360754_178360757del
DNA change (hg38) g.177439600_177439603del
Published as 372_375del
ISCN -
DB-ID AGA_000014
Variant remarks 1 Pakistani AGU patient
Reference PubMed: Saarela et al. 2001
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 12:34:27 +02:00 (CEST)
Date last edited 2020-06-16 16:39:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGA NM_000027.3 +/+ 3 c.373_376del r.(373_376del) p.(Thr125Phefs*2)


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