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Mutations on the Protein: NP_001191230 From Positions: 677 To 714

10
0
0
10



OMIM Disease: 104760.0009
p.ALA695THR
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0011
p.ILE698VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0019
p.LEU687VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT


OMIM Disease: 104760.0017
p.THR696ALA
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0015
p.THR696ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0004
p.VAL699GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0002
p.VAL699ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0021
p.VAL699LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0012
p.VAL697MET
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0003
p.VAL699PHE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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