Mutations on the Protein: Q99707 From Positions: 886 To 949
dbSNP Polymorphism: rs1805087 
Swiss-Prot Disease: VAR_004330 
p.HIS920ASP
N/A
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N/A
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Homocystinuria-megaloblastic anemia, cblG complementation type (HMAG)
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OMIM Disease: 156570.0003 
p.HIS920ASP
N/A
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N/A
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HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblG COMPLEMENTATION TYPE
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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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