Variant #0000000734 (NC_000007.13:g.44193002G>A, NM_000162.3:c.106C>T (GCK))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.44193002G>A
Reference -
DB-ID GCK_000014
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2026-06-29 05:51:33 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
GCK NM_000162.3 +?/+? - c.106C>T r.(?) p.(Arg36Trp) likely pathogenic