DMD c.227_228delinsTG ;(p.N76M)

Variant ID: X-32862936-AT-CA

NM_004006.2(DMD):c.227_228delinsTG;(p.N76M)

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: N76M
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Redundant Functions for Nap1 and Chz1 in H2A.Z Deposition.

Scientific Reports
Dronamraju, Raghuvar R; Ramachandran, Srinivas S; Jha, Deepak K DK; Adams, Alexander T AT; DiFiore, Julia V JV; Parra, Michael A MA; Dokholyan, Nikolay V NV; Strahl, Brian D BD
Publication Date: 2017-09-07

Variant appearance in text: DMD: N76M
PubMed Link: 28883625
Variant Present in the following documents:
  • Main text
  • 41598_2017_11003_MOESM1_ESM.pdf
  • 41598_2017_Article_11003.pdf
View BVdb publication page