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Mutations on the Protein: O43602 From Positions: 176 To 198

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Swiss-Prot Disease: VAR_007827
p.ARG183SER
N/A
N/A
Lissencephaly, X-linked 1 (LISX1)


Swiss-Prot Disease: VAR_007826
p.GLY181ALA
N/A
N/A
Subcortical band heterotopia X-linked (SBHX)


Swiss-Prot Disease: VAR_026028
p.ILE185THR
N/A
N/A
Subcortical band heterotopia X-linked (SBHX)


Swiss-Prot Disease: VAR_026027
p.LEU178ARG
N/A
N/A
Subcortical band heterotopia X-linked (SBHX)


OMIM Disease: 300121.0013
p.ARG196HIS
N/A
N/A
LISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED


OMIM Disease: 300121.0002
p.ARG192TRP
N/A
N/A
LISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED






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