Variant #0000001690 (NC_000009.11:g.6540109G>T, NM_000170.2:c.2607C>A (GLDC))

Chromosome 9
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.6540109G>T
DNA change (hg38) g.6540109G>T
Published as 3 cDNA splice variants: exon 22 del, exon 22-23 del and 87-bp ins
ISCN -
DB-ID GLDC_000105 See all 2 reported entries
Variant remarks 9 homozygous consanguineous Israeli Bedouin kindred with GCE
Reference PubMed: Flusser et al. 2005
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-09-05 10:24:55 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GLDC NM_000170.2 +/+ 22 c.2607C>A r.[=, spl] p.[=, ?] -


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.