Mutations on the Protein: Q12768 From Positions: 580 To 637
Swiss-Prot Disease: VAR_031956 
p.LEU619PHE
N/A
| |
N/A
|
|---|
Spastic paraplegia 8, autosomal dominant (SPG8)
|
|---|
Swiss-Prot Disease: VAR_031957 
p.VAL626PHE
N/A
| |
N/A
|
|---|
Spastic paraplegia 8, autosomal dominant (SPG8)
|
|---|
OMIM Disease: 610657.0002 
p.LEU619PHE
N/A
| |
N/A
|
|---|
SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT
|
|---|
OMIM Disease: 610657.0001 
p.VAL626PHE
N/A
| |
N/A
|
|---|
SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT
|
|---|
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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