Variant #0000000072 (NC_000007.13:g.44185198_44185215del, NM_000162.3:c.1134_1151del (GCK))

Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.44185198_44185215del
Reference -
DB-ID GCK_000002
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 2019-03-18 14:20:27 +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 ./+? 9 c.1134_1151del r.(?) p.(Ala379_Ala384del)