Variant #0000001525 (NC_000004.11:g.178361514_178361515del, NM_000027.3:c.200_201del (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.178361514_178361515del
DNA change (hg38) g.177440360_177440361del
Published as c.199_200delGA
ISCN -
DB-ID AGA_000007 See all 2 reported entries
Variant remarks 7 Finnish AGU families
Reference PubMed: Isoniemi et al. 1995
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 10:22:39 +02:00 (CEST)
Date last edited 2020-06-16 16:39:37 +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 +/+ 2 c.200_201del r.200_201delag p.Glu67Alafs*3


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