Variant #0000001543 (NC_000004.11:g.178354404C>T, NM_000027.3:c.904G>A (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.178354404C>T
DNA change (hg38) g.177433250C>T
Published as -
ISCN -
DB-ID AGA_000025
Variant remarks 1 Turkish AGU patient (hom)
Reference PubMed: Ikonen et al. 1991
ClinVar ID -
dbSNP ID rs121964905
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 14:22:03 +02:00 (CEST)
Date last edited 2019-02-27 20:52:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGA NM_000027.3 +/+ 8 c.904G>A r.904g>a p.Gly302Arg


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