Variant #0000001579 (NC_000009.11:g.(?_6645245)_(6645307_?)del, NC_000009.11(NM_000170.2):c.(?_-1)_(255+1_256-1)del (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.(?_6645245)_(6645307_?)del
DNA change (hg38) -
Published as del Exon 1
ISCN -
DB-ID GLDC_000006 See all 6 reported entries
Variant remarks 9 GCE families
Reference PubMed: Kure et al. 2002, PubMed: Kure et al. 2006, PubMed: Contel et al. 2006, PubMed: Kanno et al. 2007
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 No license selected
Created by Anne Polvi
Date created 2012-08-31 12:34:33 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +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 +/+ _1_1i c.(?_-1)_(255+1_256-1)del r.? p.? -


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