Variant #0000001684 (NC_000009.11:g.6595109G>A, NM_000170.2:c.1166C>T (GLDC))

Chromosome 9
Allele Both (homozygous)
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.6595109G>A
DNA change (hg38) g.6595109G>A
Published as -
ISCN -
DB-ID GLDC_000099 See all 15 reported entries
Variant remarks 2 GCE families (both hom)
Reference PubMed: Dinopoulos et al. 2005
ClinVar ID -
dbSNP ID rs121964979
Origin SUMMARY record
Segregation yes
Frequency 0/200 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-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 09:37:05 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +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 +?/+? 9 c.1166C>T r.(1166c>u) p.(Ala389Val) -


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