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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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