Variant #0000001624 (NC_000009.11:g.6554783T>C, NC_000009.11(NM_000170.2):c.2203-2A>G (GLDC))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6554783T>C
DNA change (hg38) g.6554783T>C
Published as IVS18-2A tagGTG>tggGTG
ISCN -
DB-ID GLDC_000041 See all 4 reported entries
Variant remarks 1 Hispanic GCE patient (het), 1 Turkish GCE patient (hom) and 1 GCE family
Reference PubMed: Toone et al. 2002, PubMed: Kure et al. 2006, PubMed: Ezgu et al. 2014
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 2012-09-04 11:34:23 +02:00 (CEST)
Date last edited 2020-06-25 12:33:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GLDC NM_000170.2 +?/+? 18i c.2203-2A>G r.spl? p.? -


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