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Mutations on the Protein: P69905 From Positions: 57 To 64

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Swiss-Prot Polymorphism: VAR_002776
p.GLY58ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002778
p.GLY60ASP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002779
p.GLY60VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_025388
p.HIS59GLN
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002777
p.HIS59TYR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002774
p.LYS57ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002780
p.LYS61ASN
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002782
p.LYS62ASN
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002775
p.LYS57THR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002783
p.LYS62THR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002784
p.VAL63MET
N/A
N/A
N/A


OMIM Disease: 141800.0118
p.ALA63ASP
N/A
N/A
HEMOGLOBIN PONTOISE||HEMOGLOBIN J (PONTOISE)


OMIM Disease: 141800.0086
p.GLY57ARG
N/A
N/A
HEMOGLOBIN L (PERSIAN GULF)


OMIM Disease: 141800.0107
p.GLY57ASP
N/A
N/A
HEMOGLOBIN NORFOLK||HEMOGLOBIN J (NORFOLK);;||HEMOGLOBIN KAGOSHIMA;;||HEMOGLOBIN NISHIK


OMIM Disease: 141800.0174
p.GLY59ASP
N/A
N/A
HEMOGLOBIN ADANA||HEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED


OMIM Disease: 141800.0151
p.GLY59VAL
N/A
N/A
HEMOGLOBIN TOTTORI


OMIM Disease: 141800.0092
p.HIS58TYR
N/A
N/A
HEMOGLOBIN M (BOSTON)||HEMOGLOBIN GOTHENBURG;;||HEMOGLOBIN M (GOTHENBURG);;||HEMOGLOBIN M (OSAKA);;||HEMOGLOBIN M (KISKU


OMIM Disease: 141800.0160
p.LYS60ASN
N/A
N/A
HEMOGLOBIN ZAMBIA


OMIM Disease: 141800.0024
p.LYS60GLU
N/A
N/A
HEMOGLOBIN DAGESTAN


OMIM Disease: 141800.0059
p.LYS61THR
N/A
N/A
HEMOGLOBIN J (ANATOLIA)


OMIM Disease: 141850.0065
p.GLY59ARG
N/A
N/A
HEMOGLOBIN ZURICH ALBISRIEDEN||ALPHA-PLUS-THALASSEMIA, INCLUDED


OMIM Disease: 141850.0073
p.GLY59ASP
N/A
N/A
HEMOGLOBIN H HYDROPS FETALIS SYNDROME


OMIM Disease: 141850.0039
p.HIS58GLN
N/A
N/A
HEMOGLOBIN BOGHE


OMIM Disease: 141850.0008
p.LYS61ASN
N/A
N/A
HEMOGLOBIN J (BUDA)||ERYTHROCYTOSIS


OMIM Disease: 141850.0006
p.VAL62MET
N/A
N/A
HEMOGLOBIN EVANS






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