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Mutations on the Protein: NP_005563 From Positions: 458 To 486

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OMIM Disease: 150330.0025
p.ARG471CYS
N/A
N/A
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL


OMIM Disease: 150330.0010
p.ARG482GLN
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0012
p.ARG482LEU
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0011
p.ARG482TRP
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0015
p.GLY465ASP
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2






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