##gff-version 3
Q7L592	UniProtKB	Transit peptide	1	46	.	.	.	Note=Mitochondrion;Ontology_term=ECO:0000255;evidence=ECO:0000255	
Q7L592	UniProtKB	Chain	47	441	.	.	.	ID=PRO_0000315672;Note=Protein arginine methyltransferase NDUFAF7%2C mitochondrial	
Q7L592	UniProtKB	Alternative sequence	73	99	.	.	.	ID=VSP_030606;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:17974005;Dbxref=PMID:17974005	
Q7L592	UniProtKB	Alternative sequence	157	227	.	.	.	ID=VSP_030607;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:17974005;Dbxref=PMID:17974005	
Q7L592	UniProtKB	Natural variant	39	39	.	.	.	ID=VAR_038274;Note=P->A;Dbxref=dbSNP:rs2714473	
Q7L592	UniProtKB	Natural variant	266	266	.	.	.	ID=VAR_079608;Note=Found in patients with myopia%3B likely pathogenic%3B may decrease mitochondrial complex I activity%3B decreases the production of ATP%3B decreases reactive oxygen species production. D->E;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:28837730;Dbxref=PMID:28837730	
Q7L592	UniProtKB	Mutagenesis	124	124	.	.	.	Note=Loss of function. G->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:24838397;Dbxref=PMID:24838397