Variant #0000000676 (NC_000007.13:g.44189445T>G, NM_000162.3:c.593A>C (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.44189445T>G
Reference -
DB-ID GCK_000012
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 2025-10-06 07:23:22 +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.593A>C r.(?) p.(Asp198Ala) likely pathogenic