Variant #0000001679 (NC_000009.11:g.6540050C>G, NC_000009.11(NM_000170.2):c.2665+1G>C (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.6540050C>G
DNA change (hg38) g.6540050C>G
Published as -
ISCN -
DB-ID GLDC_000094 See all 14 reported entries
Variant remarks 2 GCE families
Reference PubMed: Kure et al. 2006
ClinVar ID -
dbSNP ID rs149070244
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-09-05 09:27:55 +02:00 (CEST)
Date last edited 2020-06-25 12:32:58 +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 +?/+? 22i c.2665+1G>C r.spl? p.? -


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