Variant #0000001632 (NC_000009.11:g.6604637G>A, NM_000170.2:c.1009C>T (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.6604637G>A
DNA change (hg38) g.6604637G>A
Published as -
ISCN -
DB-ID GLDC_000048 See all 16 reported entries
Variant remarks 1 German GCE patient (Patient 24; com-het)
Reference PubMed: Conter et al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2012-09-04 12:56:06 +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 +/+ 7 c.1009C>T r.(1009c>u) p.(Arg337*) -


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