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Mutations on the Protein: NP_958816 From Positions: 676 To 713

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0
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10



OMIM Disease: 104760.0009
p.ALA694THR
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0011
p.ILE697VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0019
p.LEU686VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT


OMIM Disease: 104760.0017
p.THR695ALA
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0015
p.THR695ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0004
p.VAL698GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0002
p.VAL698ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0021
p.VAL698LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0012
p.VAL696MET
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0003
p.VAL698PHE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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