Run ID: ERR4815225
Sample name:
Date: 01-04-2023 13:44:36
Number of reads: 357307
Percentage reads mapped: 33.82
Strain: lineage1.2.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.5 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.7 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6918 | p.His560Arg | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.86 |
gyrA | 9564 | p.Tyr755Asn | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759656 | c.-151A>C | upstream_gene_variant | 0.33 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.4 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.6 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.4 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.6 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.33 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.5 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.5 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.6 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.4 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.5 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.38 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.38 |
rpoB | 761557 | p.Ala584Gly | missense_variant | 0.3 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.2 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.3 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.3 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.33 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.45 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.5 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.5 |
rpoB | 761618 | c.1812C>T | synonymous_variant | 0.22 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.4 |
rpoB | 761642 | c.1836G>C | synonymous_variant | 0.4 |
rpoB | 761643 | p.Val613Ile | missense_variant | 0.33 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.4 |
rpoB | 761649 | p.Ser615Pro | missense_variant | 0.4 |
rpoB | 761654 | p.Glu616Asp | missense_variant | 0.5 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.4 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.5 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.5 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.5 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.5 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.5 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.22 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.22 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.25 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.29 |
rpoB | 762313 | p.Gly836Asp | missense_variant | 0.2 |
rpoB | 762731 | p.Gln975His | missense_variant | 0.18 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.33 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.38 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.33 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.33 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.33 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.27 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.23 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.23 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.42 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.53 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.62 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.64 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.6 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.6 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.18 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.56 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.5 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.46 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.4 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.22 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.25 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.25 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.25 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.29 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.29 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.44 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.3 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.18 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.45 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.14 |
rpoC | 763606 | c.237C>A | synonymous_variant | 0.21 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.2 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.42 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.27 |
rpoC | 763619 | p.Arg84Ser | missense_variant | 0.29 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.25 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.29 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.47 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.22 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.12 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.14 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.29 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.15 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.19 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.12 |
rpoC | 763674 | p.Thr102Arg | missense_variant | 0.12 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.5 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.45 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.57 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.54 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.54 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.43 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.36 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.46 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.45 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.46 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.46 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.15 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.58 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.33 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.5 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.67 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.67 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.67 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.43 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.43 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.5 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.5 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.33 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.43 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.43 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.33 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.33 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>A | synonymous_variant | 0.33 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.38 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.22 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.22 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.43 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.29 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.29 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.33 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.29 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.29 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.5 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.5 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.5 |
fbiC | 1303217 | p.Arg96Pro | missense_variant | 0.33 |
fbiC | 1305082 | p.His718Tyr | missense_variant | 1.0 |
fbiC | 1305151 | p.Pro741Ser | missense_variant | 0.25 |
Rv1258c | 1406129 | p.Asp404Glu | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417403 | c.-56G>A | upstream_gene_variant | 0.4 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472256 | n.411T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473293 | n.1449A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.78 |
rrl | 1473390 | n.-268A>C | upstream_gene_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474588 | n.931A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474629 | n.972G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474652 | n.995T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474715 | n.1060_1061delAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474765 | n.1108A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474774 | n.1117A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476624 | n.2967T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476645 | n.2988A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476675 | n.3018C>A | non_coding_transcript_exon_variant | 0.67 |
inhA | 1674658 | p.Arg153Trp | missense_variant | 0.33 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.18 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.2 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.2 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.2 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.18 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.3 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.33 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.4 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.67 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.67 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.45 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.4 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.55 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.5 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.6 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.67 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.56 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.53 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.29 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.3 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.25 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.23 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.23 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156140 | c.-29C>A | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168616 | p.Gln666Arg | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518299 | p.Gly62Val | missense_variant | 0.2 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746251 | p.Ala450Thr | missense_variant | 0.27 |
folC | 2746831 | c.768G>T | synonymous_variant | 0.29 |
Rv2752c | 3064889 | p.Lys435Glu | missense_variant | 1.0 |
Rv2752c | 3065155 | c.1036delG | frameshift_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339609 | c.492G>A | synonymous_variant | 0.2 |
Rv3083 | 3448656 | c.153G>T | synonymous_variant | 0.33 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3641932 | p.Arg133His | missense_variant | 0.13 |
fbiB | 3642107 | c.573G>A | synonymous_variant | 0.2 |
alr | 3841518 | c.-98C>T | upstream_gene_variant | 0.33 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 1.0 |
ddn | 3987081 | p.Gly80Cys | missense_variant | 0.4 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248720 | p.Gly736Asp | missense_variant | 0.14 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269495 | c.-659G>A | upstream_gene_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethR | 4326691 | c.-858C>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338635 | c.-114A>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |