Primary_Gene,CHROM,POS,REF,ALT,QUAL,Primary_Effect,AA_Substitution,GeneId,TranscriptId,BioType,variants_impact_LOW,variants_impact_MODERATE,variants_impact_MODIFIER,variants_effect_downstream_gene_variant,variants_effect_missense_variant,variants_effect_non_coding_transcript_exon_variant,variants_effect_synonymous_variant,variants_effect_upstream_gene_variant
bluF,Chromosome,1214839,C,T,6.51248,missense_variant,Glu213Lys,b1163,AAC74247,protein_coding,0,1,0,0,1,0,0,0
fhuB,Chromosome,172282,T,C,7.30814,missense_variant,Leu274Pro,b0153,AAC73264,protein_coding,0,1,0,0,1,0,0,0
queE,Chromosome,2905289,A,G,6.51248,missense_variant,Trp44Arg,b2777,AAC75819,protein_coding,0,1,0,0,1,0,0,0
rhsD,Chromosome,527288,G,A,14.0265,missense_variant,Arg1343Lys,b0497,AAC73599,protein_coding,0,1,0,0,1,0,0,0
ruvB,Chromosome,1945062,C,T,3.22451,missense_variant,Ala99Thr,b1860,AAC74930,protein_coding,0,1,0,0,1,0,0,0
uidR,Chromosome,1696719,C,T,4.38466,missense_variant,Gly112Arg,b1618,AAC74690,protein_coding,0,1,0,0,1,0,0,0
waaY,Chromosome,3800784,A,C,3.7766,missense_variant,Val61Gly,b3625,AAC76649,protein_coding,0,1,0,0,1,0,0,0
yagM,Chromosome,294310,C,T,10.7923,missense_variant,Glu164Lys,b0279,AAC73382,protein_coding,0,1,0,0,1,0,0,0
ycaM,Chromosome,947808,G,A,8.99921,missense_variant,Glu194Lys,b0899,AAC73985,protein_coding,0,1,0,0,1,0,0,0
ydcH,Chromosome,1498809,A,C,3.22451,missense_variant,Lys53Asn,b1426,AAC74508,protein_coding,0,1,0,0,1,0,0,0
yoaE,Chromosome,1901309,C,G,5.75677,missense_variant,Gly93Arg,b1816,AAC74886,protein_coding,0,1,0,0,1,0,0,0