Variant #0000001533 (NC_000004.11:g.178360002A>G, NM_000027.3:c.404T>C (AGA))

Chromosome 4
Allele Unknown
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.178360002A>G
DNA change (hg38) g.177438848A>G
Published as -
ISCN -
DB-ID AGA_000015
Variant remarks 2 Canadian sibs (com-het) with AGU
Reference PubMed: Laitinen et al. 1997
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 12:56:09 +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 +/+ 4 c.404T>C r.(404u>c) p.(Phe135Ser)


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