Known Diseases associated with this Protein: |  AMYOTROPHY, HEREDITARY NEURALGIC
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Domains found on the Protein Table of Mutations found on the Protein| Source ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
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| dbSNP | rs2627223 | Polymorphism | p.MET569VAL | N/A | | dbSNP | rs34587622 | Polymorphism | p.PRO138ARG | N/A | | OMIM | 604061.0001 | Disease | p.ARG81TRP | AMYOTROPHY, HEREDITARY NEURALGIC | | OMIM | 604061.0002 | Disease | p.SER86PHE | AMYOTROPHY, HEREDITARY NEURALGIC |
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 |
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164698498
septin-9 isoform b [Homo sapiens]
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