Run ID: ERR171142
Sample name:
Date: 31-03-2023 14:56:25
Number of reads: 1190195
Percentage reads mapped: 28.91
Strain: lineage4.9;lineage3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.21 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.78 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.66 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 0.14 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.16 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.67 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.8 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.77 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5056 | c.-184A>C | upstream_gene_variant | 0.1 |
gyrB | 6144 | p.His302Arg | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.27 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.39 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.37 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.15 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.11 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.12 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.12 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.12 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.14 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.16 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.15 |
rpoC | 762866 | c.-504C>T | upstream_gene_variant | 0.2 |
rpoB | 762870 | p.Met1022Gln | missense_variant | 0.19 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.34 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.4 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.41 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.39 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.41 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.45 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.36 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.33 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.37 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.14 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.28 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.27 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.28 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.12 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.11 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.11 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.12 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.13 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.11 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.16 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.38 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.43 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.43 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.42 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.48 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.47 |
rpoC | 764760 | p.Asn464Ser | missense_variant | 0.46 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.46 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.45 |
rpoC | 764776 | c.1407C>T | synonymous_variant | 0.43 |
rpoC | 764785 | c.1416C>T | synonymous_variant | 0.45 |
rpoC | 764791 | c.1422C>T | synonymous_variant | 0.39 |
rpoC | 764797 | c.1428G>T | synonymous_variant | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.37 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.47 |
rpsL | 781754 | c.195G>A | synonymous_variant | 0.18 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.24 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.24 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.25 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.23 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.3 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.28 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.33 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.32 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.32 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.32 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.35 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.34 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.16 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472080 | n.235G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.92 |
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 | 0.81 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1473392 | n.-266C>A | upstream_gene_variant | 0.17 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473721 | n.64G>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1473722 | n.65G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1473744 | n.87T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1473746 | n.89T>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473747 | n.90C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473751 | n.94C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473753 | n.96A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473852 | n.195T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474199 | n.542G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475488 | n.1831G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475515 | n.1858G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.39 |
fabG1 | 1673363 | c.-77G>T | upstream_gene_variant | 0.12 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.19 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.19 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.19 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.18 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.15 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.15 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.15 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 0.16 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.16 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.22 |
rpsA | 1834213 | c.672G>A | synonymous_variant | 0.21 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.21 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.22 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.21 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.24 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.22 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.24 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.32 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.29 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.29 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.14 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.13 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.14 |
rpsA | 1834523 | p.Glu328Gln | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.22 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.43 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.22 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.38 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.18 |
Rv2752c | 3065129 | c.1063C>T | synonymous_variant | 0.14 |
Rv2752c | 3066026 | c.165delC | frameshift_variant | 0.23 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.38 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.43 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.29 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.24 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.24 |
clpC1 | 4038851 | c.1854G>C | synonymous_variant | 0.24 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.24 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.42 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.33 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.28 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.28 |
clpC1 | 4038890 | p.Glu605Asp | missense_variant | 0.22 |
clpC1 | 4038899 | c.1806C>T | synonymous_variant | 0.21 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.2 |
clpC1 | 4039889 | c.816G>T | synonymous_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.17 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.17 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.17 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.14 |
clpC1 | 4039934 | c.771G>A | synonymous_variant | 0.14 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.14 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.12 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.12 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.12 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.12 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.12 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.14 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 0.14 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.25 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.16 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.15 |
clpC1 | 4039997 | c.708C>T | synonymous_variant | 0.15 |
clpC1 | 4040009 | c.696C>T | synonymous_variant | 0.2 |
clpC1 | 4040015 | c.690G>A | synonymous_variant | 0.19 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.19 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.17 |
clpC1 | 4040027 | c.678C>G | synonymous_variant | 0.16 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.15 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.14 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.19 |
clpC1 | 4040060 | c.645C>T | synonymous_variant | 0.17 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.14 |
embC | 4241562 | p.Arg567His | missense_variant | 0.24 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.54 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.28 |