Mutations on the Protein: P68133 From Positions: 151 To 170
Swiss-Prot Disease: VAR_062447 

p.ASP156ASN

N/A
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N/A
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Nemaline myopathy 3 (NEM3)
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Swiss-Prot Disease: VAR_011684 

p.VAL165LEU

N/A
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N/A
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Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM)
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Swiss-Prot Disease: VAR_062448 

p.VAL165MET

N/A
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N/A
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Nemaline myopathy 3 (NEM3)
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OMIM Disease: 102610.0004 

p.VAL163LEU

N/A
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N/A
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NEMALINE MYOPATHY 3
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OMIM Disease: 102610.0014 

p.VAL163MET

N/A
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N/A
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NEMALINE MYOPATHY 3
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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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