Mutations on the Protein: NP_937799 From Positions: 120 To 129
OMIM Disease: 608537.0004 

p.ARG126GLY

N/A
| |

N/A
|
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VON HIPPEL-LINDAU SYNDROME
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OMIM Disease: 608537.0003 

p.ARG126TRP

N/A
| |

N/A
|
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VON HIPPEL-LINDAU SYNDROME||PHEOCHROMOCYTOMA, INCLUDED
|
---|
OMIM Disease: 608537.0027 

p.GLN123ARG

N/A
| |

N/A
|
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VON HIPPEL-LINDAU SYNDROME
|
---|
OMIM Disease: 608537.0018 

p.LEU122PRO

N/A
| |

N/A
|
---|

RENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS
|
---|
OMIM Disease: 608537.0013 

p.VAL125PHE

N/A
| |

N/A
|
---|

VON HIPPEL-LINDAU SYNDROME
|
---|
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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