|  | Tips:  The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
|---|
 Default View:
| |
|---|
Domains found on the Protein Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
|---|
| dbSNP | rs61741619 | Polymorphism | p.ARG644HIS | N/A | | dbSNP | rs11555803 | Polymorphism | p.ARG257LYS | N/A | | dbSNP | rs3811182 | Polymorphism | p.ILE311MET | N/A | | dbSNP | rs3751501 | Polymorphism | p.SER478PHE | N/A | | dbSNP | rs61741621 | Polymorphism | p.SER645PHE | N/A | | dbSNP | rs1885097 | Polymorphism | p.SER467PRO | N/A |
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
|
7662238
apoptotic chromatin condensation inducer in the nucleus isoform 1 [Homo sapiens]
0
6
0
6
0
