Variant #0000000108 (NC_000007.13:g.44190645G>A, NM_000162.3:c.393C>T (GCK))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.44190645G>A
Reference -
DB-ID GCK_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-10-08 09:16:15 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCK NM_000162.3 ./? 4 c.393C>T r.(=) p.(=)