Variant #0000001607 (NC_000009.11:g.6610345T>C, NM_000170.2:c.482A>G (GLDC))

Chromosome 9
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6610345T>C
DNA change (hg38) g.6610345T>C
Published as -
ISCN -
DB-ID GLDC_000024 See all 5 reported entries
Variant remarks 2 Palestinian Arab sibs (hom) with GCE
Reference PubMed: Korman et al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/64 CONT
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 08:31:21 +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 +/+? 4 c.482A>G r.(482a>g) p.(Tyr161Cys) -


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