Variant #0000001645 (NC_000009.11:g.6554673C>T, NM_000170.2:c.2311G>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.6554673C>T
DNA change (hg38) g.6554673C>T
Published as -
ISCN -
DB-ID GLDC_000061 See all 12 reported entries
Variant remarks 4 or more GCE families.
Reference PubMed: Kure et al. 2004, PubMed: Conter et al. 2006, Originally published: Kure S, et al (2003) A comprehensive mutation analysis of GLDC, AMT and GCSH in glycine encephalopathy. J Inherit Metab Dis 26(Supplement 2): 132-O.
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 14:13:03 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GLDC NM_000170.2 +?/+? 19 c.2311G>A r.(2311g>a) p.(Gly771Arg) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.