Nucleotide substitution: G619T. Amino acid replacement: G32C. Residue 382 is Leu.
G19564591T
G619T
G32C | G6pd-PA; G10C | G6pd-PB; G10C | G6pd-PC
G32C
Mutation presumed to be responsible for electrophoretic variant.
electrophoretic variant: faster than ZwA suppression of Pgd-lethality: strong
Eanes.
Isolated in Europe.
Isolated in Europe.