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Mutations on the Protein: P01116 From Positions: 57 To 66

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Swiss-Prot Disease: VAR_016030
p.ALA59THR
N/A
N/A
Gastric cancer (GASC)


Swiss-Prot Polymorphism: VAR_036306
p.GLN61ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_006841
p.GLN61HIS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_026112
p.GLY60ARG
N/A
N/A
Cardiofaciocutaneous syndrome 2 (CFC2)


Swiss-Prot Disease: VAR_065146
p.GLY60SER
N/A
N/A
Noonan syndrome 3 (NS3)


Swiss-Prot Disease: VAR_026111
p.THR58ILE
N/A
N/A
Noonan syndrome 3 (NS3)


OMIM Disease: 190070.0004
p.ALA59THR
N/A
N/A
BLADDER CANCER, TRANSITIONAL CELL, SOMATIC


OMIM Disease: 190070.0009
p.GLY60ARG
N/A
N/A
CARDIOFACIOCUTANEOUS SYNDROME 2


OMIM Disease: 190070.0020
p.GLY60SER
N/A
N/A
NOONAN SYNDROME 3


OMIM Disease: 190070.0011
p.THR58ILE
N/A
N/A
NOONAN SYNDROME 3






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