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Mutations on the Protein: Q13402 From Positions: 111 To 222

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Swiss-Prot Disease: VAR_027304
p.ALA198THR
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_009318
p.ARG212CYS
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_009319
p.ARG212HIS
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_027302
p.GLY163ARG
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_009320
p.GLY214ARG
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_027301
p.HIS133ASP
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_024042
p.ILE134ASN
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Polymorphism: VAR_009317
p.ILE205VAL
N/A
N/A
N/A


Swiss-Prot Disease: VAR_027303
p.LYS164ARG
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Disease: VAR_027305
p.THR204ALA
N/A
N/A
Usher syndrome 1B (USH1B)


Swiss-Prot Polymorphism: VAR_066861
p.THR193ILE
N/A
N/A
N/A


Swiss-Prot Disease: VAR_024043
p.THR165MET
N/A
N/A
Usher syndrome 1B (USH1B)


OMIM Disease: 276903.0005
p.ARG212CYS
N/A
N/A
USHER SYNDROME, TYPE IB


OMIM Disease: 276903.0004
p.ARG212HIS
N/A
N/A
USHER SYNDROME, TYPE IB


OMIM Disease: 276903.0001
p.ARG150TER
N/A
N/A
USHER SYNDROME, TYPE IB


OMIM Disease: 276903.0019
p.ASP218ASN
N/A
N/A
DEAFNESS, AUTOSOMAL DOMINANT 11






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