Variant #0000001637 (NC_000009.11:g.6592870C>T, NM_000170.2:c.1382G>A (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.6592870C>T
DNA change (hg38) g.6592870C>T
Published as -
ISCN -
DB-ID GLDC_000053 See all 12 reported entries
Variant remarks GCE mutation
Reference PubMed: Conter et al. 2006, Published originally: Van Hove JLK, Mathieu V, Schollen E, et al (2003) Prognosis of nonketotic hyperglycinemia. J Inherit Metab Dis 26(Supplement 2): A141-O
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 13:28:30 +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 +?/+? 10 c.1382G>A r.(1382g>a) p.(Arg461Gln) -


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