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Mutations on the Protein: NP_001129602 From Positions: 607 To 643

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OMIM Disease: 104760.0005
p.ALA636GLY
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT||ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED


OMIM Disease: 104760.0023
p.ALA617THR
N/A
N/A
ALZHEIMER DISEASE, PROTECTION AGAINST


OMIM Disease: 104760.0022
p.ALA617VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1, AUTOSOMAL RECESSIVE


OMIM Disease: 104760.0016
p.ASN638ASP
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT


OMIM Disease: 104760.0010
p.GLU609ASP
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0001
p.GLU637GLN
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT


OMIM Disease: 104760.0013
p.GLU637GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1||CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT, INCLUDED


OMIM Disease: 104760.0014
p.GLU637LYS
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT


OMIM Disease: 104760.0008
p.LYS614ASN
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0008
p.MET615LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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