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Mutations on the Protein: Q8WXF7 From Positions: 140 To 167

4
3
0
1



Swiss-Prot Disease: VAR_019446
p.ALA161PRO
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_067655
p.GLN154GLU
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_065509
p.LEU157TRP
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


OMIM Disease: 606439.0008
p.LEU157TRP
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT






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