GCK c.460_462delinsATC ;(p.V154I)

Variant ID: 7-44190576-CAC-GAT

NM_000162.3(GCK):c.460_462delinsATC;(p.V154I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: V154I
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page