Mutations on the Protein: P40337 From Positions: 160 To 170
Swiss-Prot Disease: VAR_005751 
p.ARG161GLN
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005761 
p.ARG167GLN
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005753 
p.ARG161GLY
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005760 
p.ARG167GLY
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005752 
p.ARG161PRO
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005762 
p.ARG167TRP
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005755 
p.CYS162ARG
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005754 
p.CYS162PHE
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005756 
p.CYS162TRP
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005757 
p.CYS162TYR
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005758 
p.GLN164ARG
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_008102 
p.GLN164HIS
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_034998 
p.LEU163PRO
N/A
| |
N/A
|
|---|
Renal cell carcinoma (RCC)
|
|---|
Swiss-Prot Disease: VAR_008103 
p.VAL166ASP
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005763 
p.VAL170ASP
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005765 
p.VAL170GLY
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005759 
p.VAL166PHE
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
Swiss-Prot Disease: VAR_005764 
p.VAL170PHE
N/A
| |
N/A
|
|---|
Von Hippel-Lindau disease (VHLD)
|
|---|
OMIM Disease: 608537.0005 
p.ARG167GLN
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME
|
|---|
OMIM Disease: 608537.0004 
p.ARG167GLY
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME
|
|---|
OMIM Disease: 608537.0006 
p.ARG161TER
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME
|
|---|
OMIM Disease: 608537.0003 
p.ARG167TRP
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME||PHEOCHROMOCYTOMA, INCLUDED
|
|---|
OMIM Disease: 608537.0027 
p.GLN164ARG
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME
|
|---|
OMIM Disease: 608537.0018 
p.LEU163PRO
N/A
| |
N/A
|
|---|
RENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS
|
|---|
OMIM Disease: 608537.0013 
p.VAL166PHE
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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