Run ID: SRR6832644
Sample name:
Date: 04-04-2023 17:33:18
Number of reads: 359064
Percentage reads mapped: 14.69
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.87 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5451 | p.Glu71Val | missense_variant | 0.33 |
gyrB | 6302 | p.Ala355Ser | missense_variant | 0.22 |
gyrB | 6576 | c.1339delT | frameshift_variant | 0.4 |
gyrB | 6796 | p.Ile519Met | missense_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 760422 | c.616_618delCTCinsTTG | synonymous_variant | 0.25 |
rpoB | 760466 | c.660C>T | synonymous_variant | 0.33 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.3 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.3 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.3 |
rpoB | 760490 | c.684C>A | synonymous_variant | 0.3 |
rpoB | 760502 | c.696C>T | synonymous_variant | 0.33 |
rpoB | 760508 | c.702G>A | synonymous_variant | 0.33 |
rpoB | 760519 | p.Thr238Ser | missense_variant | 0.38 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.2 |
rpoB | 761594 | c.1788C>T | synonymous_variant | 0.33 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.33 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.3 |
rpoB | 761998 | c.2193_2195delGTC | disruptive_inframe_deletion | 0.3 |
rpoB | 762005 | c.2200_2201insAGC | disruptive_inframe_insertion | 0.43 |
rpoB | 762009 | p.Leu735Ile | missense_variant | 0.43 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.38 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.33 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.33 |
rpoB | 762035 | c.2229G>C | synonymous_variant | 0.27 |
rpoB | 762036 | p.Ile744Val | missense_variant | 0.25 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.18 |
rpoB | 762112 | p.Asn769Ser | missense_variant | 0.22 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.72 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.76 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.75 |
rpoB | 762173 | p.Glu789Asp | missense_variant | 0.71 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.74 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.75 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.75 |
rpoB | 762191 | c.2385C>T | synonymous_variant | 0.78 |
rpoB | 762197 | c.2391C>G | synonymous_variant | 0.8 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.8 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.87 |
rpoB | 762242 | c.2436G>A | synonymous_variant | 0.78 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.78 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.76 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.77 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.75 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.77 |
rpoB | 762290 | c.2484C>T | synonymous_variant | 0.7 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.7 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.6 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.6 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.53 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.6 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.67 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.68 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.69 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.7 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.76 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.76 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.82 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.6 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.43 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.6 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.6 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.6 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.8 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.77 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.77 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.77 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.77 |
rpoC | 763630 | c.261G>T | synonymous_variant | 0.76 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.72 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.81 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.83 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.84 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.84 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.81 |
rpoC | 763672 | c.303C>A | synonymous_variant | 0.81 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.74 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.74 |
rpoC | 763702 | c.333C>T | synonymous_variant | 0.74 |
rpoC | 763705 | c.336G>C | synonymous_variant | 0.74 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.74 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.74 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.74 |
rpoC | 763732 | c.363C>T | synonymous_variant | 0.73 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.62 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.4 |
rpoC | 764311 | c.942C>G | synonymous_variant | 0.81 |
rpoC | 764314 | c.945C>T | synonymous_variant | 0.81 |
rpoC | 764318 | p.Val317Ile | missense_variant | 0.84 |
rpoC | 764326 | c.957G>T | synonymous_variant | 0.85 |
rpoC | 764329 | c.960C>T | synonymous_variant | 0.85 |
rpoC | 764335 | c.966G>A | synonymous_variant | 0.84 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.84 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.84 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.83 |
rpoC | 764374 | c.1005C>T | synonymous_variant | 0.83 |
rpoC | 764377 | c.1008C>T | synonymous_variant | 0.83 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.83 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.83 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.77 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.7 |
rpoC | 764410 | c.1041G>T | synonymous_variant | 0.64 |
rpoC | 764422 | c.1053C>T | synonymous_variant | 0.5 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.33 |
rpoC | 764458 | c.1089G>A | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.33 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.33 |
rpoC | 764473 | c.1104C>T | synonymous_variant | 0.33 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.33 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.62 |
rpoC | 764518 | c.1149C>T | synonymous_variant | 0.62 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.62 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.73 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.7 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.7 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.75 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.89 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.94 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.94 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.91 |
rpoC | 764578 | c.1209C>T | synonymous_variant | 0.91 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.91 |
rpoC | 764582 | c.1213C>T | synonymous_variant | 0.91 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.94 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.93 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.85 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.85 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.85 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.85 |
rpoC | 764644 | c.1275G>T | synonymous_variant | 0.73 |
rpoC | 764854 | c.1485G>A | synonymous_variant | 0.4 |
rpoC | 764858 | p.Leu497Met | missense_variant | 0.6 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.71 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.83 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.85 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.85 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.83 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.83 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.92 |
rpoC | 764913 | p.Met515Lys | missense_variant | 0.92 |
rpoC | 764920 | c.1551G>T | synonymous_variant | 0.95 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.95 |
rpoC | 764926 | c.1557C>T | synonymous_variant | 0.95 |
rpoC | 764932 | c.1563C>T | synonymous_variant | 0.95 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.94 |
rpoC | 764952 | p.Val528Ala | missense_variant | 0.94 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.82 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778782 | p.Lys42Glu | missense_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.21 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.21 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.5 |
rpsL | 781799 | c.240G>C | synonymous_variant | 0.5 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.5 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.5 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.5 |
rpsL | 781829 | c.270G>T | synonymous_variant | 0.5 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.5 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.5 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.4 |
rplC | 800669 | c.-140G>T | upstream_gene_variant | 0.55 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.58 |
rplC | 800693 | c.-116A>T | upstream_gene_variant | 0.59 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.56 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.56 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.53 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.53 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.53 |
rplC | 800723 | c.-86C>A | upstream_gene_variant | 0.53 |
rplC | 800726 | c.-83G>C | upstream_gene_variant | 0.53 |
rplC | 800741 | c.-68C>T | upstream_gene_variant | 0.62 |
rplC | 800744 | c.-65G>T | upstream_gene_variant | 0.56 |
rplC | 800747 | c.-62C>T | upstream_gene_variant | 0.56 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.42 |
rplC | 800768 | c.-41C>A | upstream_gene_variant | 0.4 |
rplC | 800780 | c.-29C>G | upstream_gene_variant | 0.29 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 1.0 |
fbiC | 1305196 | p.Ala756Thr | missense_variant | 0.18 |
embR | 1417464 | c.-117C>T | upstream_gene_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.96 |
rrs | 1471922 | n.78T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1471925 | n.80_81insTG | non_coding_transcript_exon_variant | 0.89 |
rrs | 1471928 | n.83T>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472671 | n.826G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472840 | n.995A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472866 | n.1021C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472974 | n.1129A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472977 | n.1133dupT | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473132 | n.1287T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473135 | n.1290C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473346 | n.1501G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473365 | n.1520C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473390 | n.-268A>T | upstream_gene_variant | 0.22 |
rrl | 1473447 | n.-211G>T | upstream_gene_variant | 0.2 |
rrl | 1473697 | n.40C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473698 | n.41G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473718 | n.61G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1473719 | n.62G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473750 | n.93C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473751 | n.94C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1473884 | n.227C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473896 | n.239C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473911 | n.254G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473918 | n.261C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1473935 | n.278C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474112 | n.455T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474142 | n.485C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474182 | n.525C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474183 | n.526T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474199 | n.542G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474311 | n.654_655insT | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474527 | n.870T>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474542 | n.885A>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474917 | n.1260G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474918 | n.1261T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475514 | n.1857G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475522 | n.1865A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475525 | n.1868G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475562 | n.1905C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476032 | n.2375C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476033 | n.2376T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476080 | n.2423T>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476097 | n.2440C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476116 | n.2459A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476592 | n.2935G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476605 | n.2948C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.5 |
inhA | 1674535 | p.Pro112Thr | missense_variant | 0.18 |
rpsA | 1833649 | c.108C>T | synonymous_variant | 1.0 |
rpsA | 1833655 | c.114C>T | synonymous_variant | 1.0 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
rpsA | 1833664 | c.123C>T | synonymous_variant | 0.67 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.67 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.67 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.5 |
rpsA | 1833679 | c.138G>T | synonymous_variant | 0.5 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.5 |
rpsA | 1833694 | c.153G>A | synonymous_variant | 0.4 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.4 |
rpsA | 1833700 | c.159C>G | synonymous_variant | 0.4 |
rpsA | 1833709 | c.168C>A | synonymous_variant | 0.4 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.4 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.18 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.18 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.2 |
rpsA | 1834018 | c.477C>T | synonymous_variant | 0.22 |
rpsA | 1834025 | p.Gln162Glu | missense_variant | 0.2 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.2 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.27 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.38 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.38 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 0.5 |
rpsA | 1834076 | p.Asn179Gln | missense_variant | 0.55 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.6 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.6 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.67 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.67 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.67 |
rpsA | 1834108 | c.567C>A | synonymous_variant | 0.67 |
rpsA | 1834110 | p.Trp190Tyr | missense_variant | 0.57 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.57 |
rpsA | 1834135 | c.594G>T | synonymous_variant | 0.5 |
rpsA | 1834139 | c.598_599delAGinsTC | synonymous_variant | 0.5 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.33 |
rpsA | 1834186 | c.645C>T | synonymous_variant | 0.43 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.5 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.73 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.9 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.86 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.83 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.86 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.86 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.86 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.86 |
rpsA | 1834264 | c.723G>T | synonymous_variant | 0.83 |
rpsA | 1834276 | c.735C>T | synonymous_variant | 0.78 |
rpsA | 1834285 | c.744G>A | synonymous_variant | 0.75 |
rpsA | 1834288 | c.747C>T | synonymous_variant | 0.75 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.62 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.45 |
rpsA | 1834654 | c.1113G>A | synonymous_variant | 0.5 |
rpsA | 1834663 | c.1122C>T | synonymous_variant | 0.4 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.4 |
rpsA | 1834684 | c.1143C>T | synonymous_variant | 0.43 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.43 |
rpsA | 1834712 | p.Ile391Val | missense_variant | 0.38 |
rpsA | 1834720 | c.1179C>T | synonymous_variant | 0.38 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167995 | p.Ser873Ile | missense_variant | 1.0 |
Rv1979c | 2222289 | c.876C>G | synonymous_variant | 0.22 |
Rv1979c | 2222883 | c.282C>T | synonymous_variant | 0.29 |
Rv1979c | 2223077 | p.Ala30Thr | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2725978 | c.-215G>T | upstream_gene_variant | 0.5 |
ahpC | 2726022 | c.-171C>A | upstream_gene_variant | 0.25 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
ribD | 2987413 | p.Thr192Ile | missense_variant | 0.29 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
Rv3083 | 3449213 | p.Arg237Leu | missense_variant | 0.29 |
fprA | 3473888 | c.-119G>T | upstream_gene_variant | 0.2 |
fprA | 3474952 | p.Gln316Lys | missense_variant | 0.4 |
fprA | 3475053 | c.1049delG | frameshift_variant | 0.4 |
fbiB | 3641782 | p.Val83Ala | missense_variant | 0.29 |
alr | 3840582 | p.Ala280Asp | missense_variant | 0.29 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 0.33 |
clpC1 | 4038556 | p.Ile717Val | missense_variant | 0.38 |
clpC1 | 4038563 | c.2142C>T | synonymous_variant | 0.33 |
clpC1 | 4038569 | c.2136C>T | synonymous_variant | 0.33 |
clpC1 | 4038575 | c.2128_2130delCTCinsTTG | synonymous_variant | 0.38 |
clpC1 | 4038584 | c.2121G>A | synonymous_variant | 0.5 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.43 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.43 |
clpC1 | 4038632 | p.Glu691Asp | missense_variant | 0.29 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.38 |
clpC1 | 4039826 | c.879C>T | synonymous_variant | 0.5 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.55 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.6 |
clpC1 | 4039844 | c.861C>T | synonymous_variant | 0.55 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.55 |
clpC1 | 4039855 | c.850C>T | synonymous_variant | 0.5 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.46 |
clpC1 | 4039871 | p.Thr278Gln | missense_variant | 0.46 |
clpC1 | 4039877 | c.828C>T | synonymous_variant | 0.43 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.43 |
clpC1 | 4039910 | c.795C>T | synonymous_variant | 0.5 |
clpC1 | 4040508 | p.Ile66Asn | missense_variant | 0.33 |
clpC1 | 4040763 | c.-59C>A | upstream_gene_variant | 0.5 |
embC | 4240055 | p.Gly65Ser | missense_variant | 0.5 |
embC | 4240435 | c.573C>T | synonymous_variant | 0.4 |
embC | 4241891 | p.Ala677Pro | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243180 | c.-53C>A | upstream_gene_variant | 0.25 |
embA | 4243513 | p.Pro94Leu | missense_variant | 0.17 |
embA | 4244440 | p.Gly403Glu | missense_variant | 0.29 |
embA | 4246297 | p.Gln1022Arg | missense_variant | 0.25 |
ethA | 4326252 | p.Tyr408Asp | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |