Mutations on the Protein: P40337 From Positions: 85 To 96
Swiss-Prot Disease: VAR_005704 
p.GLY93ASP
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005703 
p.GLY93CYS
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005705 
p.GLY93SER
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Polymorphism: VAR_005699 
Swiss-Prot Disease: VAR_005700 
p.LEU89PRO
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Polymorphism: VAR_005701 
Swiss-Prot Disease: VAR_005693 
p.PRO86ALA
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005695 
p.PRO86ARG
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_008097 
p.PRO86HIS
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005694 
p.PRO86LEU
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005696 
p.PRO86SER
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005697 
p.TRP88ARG
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005698 
p.TRP88SER
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
OMIM Disease: 608537.0026 
p.GLY93SER
N/A
| |
N/A
|
|---|
PHEOCHROMOCYTOMA
|
|---|
OMIM Disease: 608537.0007 
p.TRP88SER
N/A
| |
N/A
|
|---|
HEMANGIOBLASTOMA, SPORADIC CEREBELLAR||VON HIPPEL-LINDAU SYNDROME, 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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