GCK c.1092C>G ;(p.C364W)

Variant ID: 7-44185257-G-C

NM_000162.3(GCK):c.1092C>G;(p.C364W)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts.

American Journal Of Human Genetics
Mirshahi, Uyenlinh L UL; Colclough, Kevin K; Wright, Caroline F CF; Wood, Andrew R AR; Beaumont, Robin N RN; Tyrrell, Jessica J; Laver, Thomas W TW; Stahl, Richard R; Golden, Alicia A; Goehringer, Jessica M JM; , ; Frayling, Timothy F TF; Hattersley, Andrew T AT; Carey, David J DJ; Weedon, Michael N MN; Patel, Kashyap A KA
Publication Date: 2022-11-03

Variant appearance in text: GCK: 1092C>G; Cys364Trp
PubMed Link: 36257325
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: GCK: C364W
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page