Mutations on the Protein: P54098 From Positions: 1177 To 1239
Swiss-Prot Disease: VAR_058897 
p.ASP1184ASN
N/A
| |
N/A
|
|---|
Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB)
|
|---|
Swiss-Prot Disease: VAR_065119 
p.ASP1186HIS
N/A
| |
N/A
|
|---|
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 (PEOA1)
|
|---|
dbSNP Polymorphism: rs3087374 
Swiss-Prot Disease: VAR_058898 
p.LYS1191ASN
N/A
| |
N/A
|
|---|
Mitochondrial DNA depletion syndrome 4A (MTDPS4A)
|
|---|
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 |
|
4
3
1
0
