DMD c.167_168delinsAG ;(p.G56E)

Variant ID: X-32867863-GC-CT

NM_004006.2(DMD):c.167_168delinsAG;(p.G56E)

This variant was identified in 2 publications

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: DMD: G56E
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Computational design of a PAK1 binding protein.

Journal Of Molecular Biology
Jha, Ramesh K RK; Leaver-Fay, Andrew A; Yin, Shuangye S; Wu, Yibing Y; Butterfoss, Glenn L GL; Szyperski, Thomas T; Dokholyan, Nikolay V NV; Kuhlman, Brian B
Publication Date: 2010-07-09

Variant appearance in text: DMD: G56E
PubMed Link: 20460129
Variant Present in the following documents:
  • Main text
View BVdb publication page