Mutations on the Protein: Q92736 From Positions: 2235 To 2484
Swiss-Prot Disease: VAR_044093 

p.ALA2387PRO

N/A
| |

N/A
|
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Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
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Swiss-Prot Disease: VAR_044095 

p.ALA2403THR

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_011399 

p.ARG2474SER

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_011398 

p.ASN2386ILE

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_044092 

p.GLU2311ASP

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_011397 

p.PRO2328SER

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_011396 

p.SER2246LEU

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_044094 

p.TYR2392CYS

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
Swiss-Prot Disease: VAR_023694 

p.VAL2306ILE

N/A
| |

N/A
|
---|

Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopa
|
---|
OMIM Disease: 180902.0002 

p.ARG2474SER

N/A
| |

N/A
|
---|

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1
|
---|
OMIM Disease: 180902.0005 

p.ASN2386ILE

N/A
| |

N/A
|
---|

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
|
---|
OMIM Disease: 180902.0007 

p.PRO2328SER

N/A
| |

N/A
|
---|

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1
|
---|
OMIM Disease: 180902.0001 

p.SER2246LEU

N/A
| |

N/A
|
---|

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1
|
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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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