Variant #0000001617 (NC_000009.11:g.6605145C>G, NM_000170.2:c.847G>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.6605145C>G
DNA change (hg38) g.6605145C>G
Published as -
ISCN -
DB-ID GLDC_000034 See all 6 reported entries
Variant remarks 1 Newfoundland GCE patient (Patient 1; het)
Reference PubMed: Toone et al. 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-09-04 10:22:30 +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 +?/+? 6 c.847G>C r.(847g>c) p.(Ala283Pro) -


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