PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8471773-4 1993 From these 43 samples, we have identified five different types of nucleotide substitutions in the G6PD gene: at cDNA 1388 from G to A (Arg to His); at cDNA 1376 from G to T (Arg to Leu); at cDNA 1024 from C to T (Leu to Phe); at cDNA 392 from G to T (Gly to Val); at cDNA 95 from A to G (His to Arg). Leucine 181-184 glucose-6-phosphate dehydrogenase Homo sapiens 98-102 31374327-10 2019 A base substitution mutation was identified at c.1466 (c.1466G>T) of G6PD on chromosome X of the patient, which resulted in an amino acid change from arginine to leucine at p.489 (p.R489L). Leucine 165-172 glucose-6-phosphate dehydrogenase Homo sapiens 72-76 8807322-0 1996 G6PD NanKang (517 T-->C; 173 Phe-->Leu): a new Chinese G6PD variant associated with neonatal jaundice. Leucine 41-44 glucose-6-phosphate dehydrogenase Homo sapiens 0-4 8807322-0 1996 G6PD NanKang (517 T-->C; 173 Phe-->Leu): a new Chinese G6PD variant associated with neonatal jaundice. Leucine 41-44 glucose-6-phosphate dehydrogenase Homo sapiens 61-65 10745013-5 2000 RESULTS: We have determined the first crystal structure of a human G6PD (the mutant Canton, Arg459-->Leu) at 3 A resolution. Leucine 104-107 glucose-6-phosphate dehydrogenase Homo sapiens 67-71 10627140-5 1998 The molecular basis of this new Class III G6PD variant is a G-->T mutation at nucleotide 34 in the exon 2, which predicts a Val-->Leu aminoacid substitution at codon 12. Leucine 130-133 glucose-6-phosphate dehydrogenase Homo sapiens 42-46 8471773-4 1993 From these 43 samples, we have identified five different types of nucleotide substitutions in the G6PD gene: at cDNA 1388 from G to A (Arg to His); at cDNA 1376 from G to T (Arg to Leu); at cDNA 1024 from C to T (Leu to Phe); at cDNA 392 from G to T (Gly to Val); at cDNA 95 from A to G (His to Arg). Leucine 213-216 glucose-6-phosphate dehydrogenase Homo sapiens 98-102 1999409-4 1991 Although the patients were all unrelated, G6PD Marion, Gastonia, and Minnesota each had identical mutations, a G----T at nucleotide (nt) 637 in exon 6 leading to a Val----Leu substitution at amino acid 213. Leucine 171-174 glucose-6-phosphate dehydrogenase Homo sapiens 42-46