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Mutations on the Protein: P05067 From Positions: 693 To 732

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14



Swiss-Prot Disease: VAR_000019
p.ALA713THR
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Polymorphism: VAR_000018
p.ALA713VAL
N/A
N/A
N/A


Swiss-Prot Disease: VAR_014217
p.ASP694ASN
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


Swiss-Prot Disease: VAR_000017
p.GLU693GLN
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


Swiss-Prot Disease: VAR_014215
p.GLU693GLY
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_014216
p.GLU693LYS
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


Swiss-Prot Disease: VAR_000020
p.ILE716VAL
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_010109
p.LEU723PRO
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_032276
p.LEU705VAL
N/A
N/A
Cerebral amyloid angiopathy, APP-related (CAA-APP)


Swiss-Prot Disease: VAR_032277
p.THR714ALA
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_014218
p.THR714ILE
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_000022
p.VAL717GLY
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_000021
p.VAL717ILE
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_014219
p.VAL717LEU
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_010108
p.VAL715MET
N/A
N/A
Alzheimer disease 1 (AD1)


Swiss-Prot Disease: VAR_000023
p.VAL717PHE
N/A
N/A
Alzheimer disease 1 (AD1)


OMIM Disease: 104760.0009
p.ALA713THR
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0016
p.ASN694ASP
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT


OMIM Disease: 104760.0001
p.GLU693GLN
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT


OMIM Disease: 104760.0013
p.GLU693GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1||CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT, INCLUDED


OMIM Disease: 104760.0014
p.GLU693LYS
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT


OMIM Disease: 104760.0011
p.ILE716VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0019
p.LEU705VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT


OMIM Disease: 104760.0017
p.THR714ALA
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0015
p.THR714ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0004
p.VAL717GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0002
p.VAL717ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0021
p.VAL717LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0012
p.VAL715MET
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0003
p.VAL717PHE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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