Variant #0000001660 (NC_000009.11:g.6592182dup, NM_000170.2:c.1444dup (GLDC))

Chromosome 9
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.6592182dup
DNA change (hg38) g.6592182dup
Published as c.1443insG
ISCN -
DB-ID GLDC_000076 See all 2 reported entries
Variant remarks 1 Caucasian GCE patient (P104; com-het)
Reference PubMed: Kure et al. 2006
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 2012-09-05 08:46:44 +02:00 (CEST)
Date last edited 2020-06-25 12:34:58 +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 +/+ 11 c.1444dup r.(?) p.(Asp482Glyfs*10) -


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