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