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Mutations on the Protein: Q8WXF7 From Positions: 391 To 419

7
3
0
4


Swiss-Prot Disease: VAR_065512
p.ARG415TRP
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_065511
p.MET408VAL
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_067658
p.PHE413VAL
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


OMIM Disease: 606439.0013
p.ARG416CYS
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT


OMIM Disease: 606439.0014
p.ARG415GLN
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT


OMIM Disease: 606439.0007
p.ARG415TRP
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT


OMIM Disease: 606439.0006
p.MET408VAL
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT






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