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Mutations on the Protein: NP_958817 From Positions: 626 To 660

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0
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10



OMIM Disease: 104760.0009
p.ALA638THR
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0011
p.ILE641VAL
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0019
p.LEU630VAL
N/A
N/A
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT


OMIM Disease: 104760.0017
p.THR639ALA
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0015
p.THR639ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0004
p.VAL642GLY
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0002
p.VAL642ILE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0021
p.VAL642LEU
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0012
p.VAL640MET
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1


OMIM Disease: 104760.0003
p.VAL642PHE
N/A
N/A
ALZHEIMER DISEASE, FAMILIAL, 1






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