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Mutations on the Protein: NP_001129603 From Positions: 561 To 594

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OMIM Disease: 104760.0005
p.ALA582GLY
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT||ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED


OMIM Disease: 104760.0023
p.ALA563THR
N/A
N/A
ALZHEIMER DISEASE, PROTECTION AGAINST


OMIM Disease: 104760.0022
p.ALA563VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1, AUTOSOMAL RECESSIVE


OMIM Disease: 104760.0016
p.ASN584ASP
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT


OMIM Disease: 104760.0001
p.GLU583GLN
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT


OMIM Disease: 104760.0013
p.GLU583GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1||CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT, INCLUDED


OMIM Disease: 104760.0014
p.GLU583LYS
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT


OMIM Disease: 104760.0008
p.MET561LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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