Variant #0000036142 (NC_000009.11:g.6565421T>C, NM_000170.2:c.1859A>G (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.6565421T>C
DNA change (hg38) g.6565421T>C
Published as -
ISCN -
DB-ID GLDC_000109 See all 2 reported entries
Variant remarks 1 GCE patient (het)
Reference PubMed: Kanekar et al. 2013
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 2014-04-03 17:40:23 +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 +?/+? 15 c.1859A>G r.(?) p.(Gln620Arg) -


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