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)
|
|---|
Swiss-Prot Disease: VAR_011684 
p.VAL165LEU
N/A
| |
N/A
|
|---|
Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM)
|
|---|
Swiss-Prot Disease: VAR_062448 
p.VAL165MET
N/A
| |
N/A
|
|---|
Nemaline myopathy 3 (NEM3)
|
|---|
OMIM Disease: 102610.0004 
p.VAL163LEU
N/A
| |
N/A
|
|---|
NEMALINE MYOPATHY 3
|
|---|
OMIM Disease: 102610.0014 
p.VAL163MET
N/A
| |
N/A
|
|---|
NEMALINE MYOPATHY 3
|
|---|
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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