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Mutations on the Protein: P11413 From Positions: 180 To 206

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5
0
4




Swiss-Prot Polymorphism: VAR_002474
p.ARG198CYS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_002475
p.ARG198PRO
N/A
N/A
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA)


Swiss-Prot Polymorphism: VAR_002472
p.ARG182TRP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002471
p.ASP181VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002473
p.SER188PHE
N/A
N/A
N/A


OMIM Disease: 305900.0035
p.ARG197GLN
N/A
N/A
G6PD MEXICO CITY


OMIM Disease: 305900.0027
p.ARG197LEU
N/A
N/A
G6PD A-


OMIM Disease: 305900.0011
p.PHE186LEU
N/A
N/A
G6PD HARILAOU


OMIM Disease: 305900.0024
p.VAL183LEU
N/A
N/A
G6PD GASTONIA||G6PD MARION;;||G6PD MINNESOTA;;||ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY






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