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Mutations on the Protein: NP_000035 From Positions: 736 To 782

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OMIM Disease: 313700.0011
p.ALA771THR
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL


OMIM Disease: 313700.0010
p.ARG772CYS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0003
p.ARG773CYS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0015
p.ARG773HIS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0057
p.GLY743GLU
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0056
p.GLY743VAL
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL||ANDROGEN INSENSITIVITY, COMPLETE, INCLUDED


OMIM Disease: 313700.0039
p.MET780ILE
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0059
p.SER740CYS
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL


OMIM Disease: 313700.0008
p.TYR761CYS
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL






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