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| | 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. |
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Domains found on the Protein Table of Mutations found on the ProteinSource ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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Swiss-Prot | VAR_042034 | Polymorphism | p.ARG764CYS | N/A | dbSNP | rs77524207 | Polymorphism | p.ARG340GLN | N/A | Swiss-Prot | VAR_066460 | Polymorphism | p.ARG481GLY | N/A | Swiss-Prot | VAR_066469 | Polymorphism | p.ARG748GLY | N/A | Swiss-Prot | VAR_066466 | Polymorphism | p.ASN659LYS | N/A | Swiss-Prot | VAR_066467 | Polymorphism | p.ASN659SER | N/A | Swiss-Prot | VAR_042037 | Polymorphism | p.ASP1071ASN | N/A | Swiss-Prot | VAR_066472 | Polymorphism | p.ASP842TYR | N/A | Swiss-Prot | VAR_066471 | Polymorphism | p.ASP842VAL | N/A | Swiss-Prot | VAR_042036 | Polymorphism | p.GLU996LYS | N/A | Swiss-Prot | VAR_042035 | Polymorphism | p.GLY829ARG | N/A | Swiss-Prot | VAR_042033 | Polymorphism | p.GLY426ASP | N/A | Swiss-Prot | VAR_042032 | Polymorphism | p.GLY79ASP | N/A | Swiss-Prot | VAR_066464 | Polymorphism | p.HIS570ARG | N/A | Swiss-Prot | VAR_066465 | Polymorphism | p.HIS650GLN | N/A | Swiss-Prot | VAR_066463 | Polymorphism | p.ILE562MET | N/A | Swiss-Prot | VAR_066461 | Polymorphism | p.LEU507PRO | N/A | Swiss-Prot | VAR_066468 | Polymorphism | p.LEU705PRO | N/A | dbSNP | rs35597368 | Polymorphism | p.SER478PRO | N/A | Swiss-Prot | VAR_066474 | Disease | p.TYR849CYS | Gastrointestinal stromal tumor (GIST) | Swiss-Prot | VAR_066475 | Polymorphism | p.TYR849SER | N/A | Swiss-Prot | VAR_066462 | Polymorphism | p.VAL561ASP | N/A | OMIM | 173490.0011 | Disease | p.ALA401ASP | VARIANT OF UNKNOWN SIGNIFICANCE | OMIM | 173490.0009 | Disease | p.ASP846TYR | GASTROINTESTINAL STROMAL TUMOR, FAMILIAL | OMIM | 173490.0001 | Disease | p.ASP842VAL | GASTROINTESTINAL STROMAL TUMOR, SOMATIC | OMIM | 173490.0008 | Disease | p.THR674ILE | HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB | OMIM | 173490.0013 | Disease | p.THR1052MET | VARIANT OF UNKNOWN SIGNIFICANCE | OMIM | 173490.0010 | Disease | p.TYR555CYS | GASTROINTESTINAL STROMAL TUMOR, FAMILIAL | OMIM | 173490.0012 | Disease | p.VAL544ALA | VARIANT OF UNKNOWN SIGNIFICANCE | OMIM | 173490.0004 | Disease | p.VAL561ASP | GASTROINTESTINAL STROMAL TUMOR, SOMATIC||GASTROINTESTINAL STROMAL TUMOR, FAMILIAL, INCLUDED |
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.
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