Known Diseases associated with this Protein: |  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
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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 | rs7820984 | Polymorphism | p.MET76VAL | N/A | | OMIM | 123980.0002 | Disease | p.LEU215PHE | MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 | | OMIM | 123980.0001 | Disease | p.TRP96CYS | MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 |
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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21359867
cytochrome c1, heme protein, mitochondrial [Homo sapiens]
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