Mutations on the Protein: P19429 From Positions: 189 To 200
Swiss-Prot Disease: VAR_016084 
p.ARG192HIS
N/A
| |
N/A
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Cardiomyopathy, familial restrictive 1 (RCM1)
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Swiss-Prot Disease: VAR_016085 
p.ASP196ASN
N/A
| |
N/A
|
|---|
Cardiomyopathy, familial hypertrophic 7 (CMH7)
|
|---|
Swiss-Prot Disease: VAR_016083 
p.ASP190HIS
N/A
| |
N/A
|
|---|
Cardiomyopathy, familial restrictive 1 (RCM1)
|
|---|
OMIM Disease: 191044.0006 
p.ARG192HIS
N/A
| |
N/A
|
|---|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1
|
|---|
OMIM Disease: 191044.0004 
p.ASP196ASN
N/A
| |
N/A
|
|---|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
|
|---|
OMIM Disease: 191044.0005 
p.ASP190GLY
N/A
| |
N/A
|
|---|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7||CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1, INCLUDED
|
|---|
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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