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Mutations on the Protein: P69905 From Positions: 28 To 36

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4
0
7




Swiss-Prot Polymorphism: VAR_025002
p.ARG32LYS
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002752
p.ARG32SER
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002751
p.GLU31LYS
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002753
p.LEU35ARG
N/A
N/A
N/A


OMIM Disease: 141800.0111
p.GLU30LYS
N/A
N/A
HEMOGLOBIN O (PADOVA)


OMIM Disease: 141800.0112
p.LEU34ARG
N/A
N/A
HEMOGLOBIN OGI||HEMOGLOBIN QUEENS


OMIM Disease: 141850.0055
p.ARG31SER
N/A
N/A
HEMOGLOBIN PRATO


OMIM Disease: 141850.0054
p.GLU30GLN
N/A
N/A
HEMOGLOBIN G (HONOLULU)||HEMOGLOBIN G (HONG KONG);;||HEMOGLOBIN G (SINGAPORE);;||HEMOGLOBIN G (CHINESE)


OMIM Disease: 141850.0026
p.LEU29PRO
N/A
N/A
HEMOGLOBIN AGRINIO||HEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED


OMIM Disease: 141850.0058
p.PHE33SER
N/A
N/A
HEMOGLOBIN CHARTRES


OMIM Disease: 141850.0074
p.SER35PRO
N/A
N/A
HEMOGLOBIN H HYDROPS FETALIS SYNDROME






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