Run ID: ERR2229336
Sample name:
Date: 31-03-2023 17:01:58
Number of reads: 613223
Percentage reads mapped: 37.21
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.94 | streptomycin |
panD | 4043931 | p.Met117Ile | missense_variant | 0.15 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5903 | p.Val222Leu | missense_variant | 0.14 |
gyrA | 6478 | c.-824G>A | upstream_gene_variant | 0.17 |
gyrB | 7256 | p.Leu673Met | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7500 | p.Asp67Tyr | missense_variant | 0.12 |
gyrA | 7640 | c.339G>A | synonymous_variant | 0.13 |
gyrA | 8326 | p.Gly342Val | missense_variant | 0.12 |
gyrA | 8352 | p.Gly351Trp | missense_variant | 0.15 |
gyrA | 8777 | c.1476C>T | synonymous_variant | 0.12 |
gyrA | 9000 | p.Ile567Val | missense_variant | 0.1 |
gyrA | 9719 | c.2418G>C | synonymous_variant | 0.2 |
fgd1 | 491683 | p.Val301Leu | missense_variant | 0.18 |
mshA | 575734 | c.387T>C | synonymous_variant | 0.11 |
mshA | 575971 | p.Asp208Glu | missense_variant | 0.15 |
ccsA | 620122 | c.232C>A | synonymous_variant | 0.14 |
rpoB | 759979 | p.Leu58Pro | missense_variant | 0.11 |
rpoB | 760444 | p.Arg213Leu | missense_variant | 0.17 |
rpoB | 761536 | p.Pro577His | missense_variant | 0.17 |
rpoB | 762146 | p.Glu780Asp | missense_variant | 0.13 |
rpoC | 763852 | c.483C>G | synonymous_variant | 0.17 |
rpoC | 764227 | c.858G>T | synonymous_variant | 0.12 |
rpoC | 764869 | c.1500C>A | synonymous_variant | 0.15 |
rpoC | 765219 | p.Glu617Gly | missense_variant | 0.14 |
rpoC | 765477 | p.Arg703Leu | missense_variant | 0.12 |
rpoC | 766229 | p.Ala954Thr | missense_variant | 0.2 |
rpoC | 766388 | p.Gly1007Cys | missense_variant | 0.13 |
rpoC | 766631 | p.Val1088Met | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776470 | p.Glu671* | stop_gained | 0.14 |
mmpL5 | 777810 | p.Arg224Gln | missense_variant | 0.12 |
mmpR5 | 778313 | c.-677G>T | upstream_gene_variant | 0.2 |
mmpL5 | 778348 | p.Val45Ile | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781523 | c.-37A>G | upstream_gene_variant | 0.11 |
rpsL | 781681 | p.Thr41Asn | missense_variant | 0.2 |
rplC | 800635 | c.-174G>T | upstream_gene_variant | 0.13 |
rplC | 801128 | p.Ala107Asp | missense_variant | 0.22 |
fbiC | 1302763 | c.-168G>T | upstream_gene_variant | 0.18 |
fbiC | 1303305 | c.375C>A | synonymous_variant | 0.22 |
fbiC | 1303516 | p.Met196Val | missense_variant | 0.25 |
fbiC | 1303646 | p.Ala239Glu | missense_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304132 | p.Ala401Gly | missense_variant | 0.22 |
fbiC | 1304894 | p.Gly655Asp | missense_variant | 0.14 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.18 |
Rv1258c | 1407103 | p.Ala80Ser | missense_variant | 0.5 |
Rv1258c | 1407200 | c.141G>T | synonymous_variant | 0.2 |
Rv1258c | 1407423 | c.-83G>A | upstream_gene_variant | 0.18 |
embR | 1416769 | c.579G>A | synonymous_variant | 0.25 |
embR | 1417215 | p.Asn45Asp | missense_variant | 0.11 |
embR | 1417446 | c.-99G>C | upstream_gene_variant | 0.33 |
atpE | 1461072 | p.Leu10Ile | missense_variant | 0.15 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.13 |
atpE | 1461264 | p.Phe74Leu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471900 | n.55C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472880 | n.1035_1036insA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473008 | n.1164delT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473479 | n.-178delC | upstream_gene_variant | 0.22 |
rrl | 1473697 | n.40C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473800 | n.143G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474283 | n.626A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474694 | n.1037C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474903 | n.1246T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475552 | n.1895G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475574 | n.1917C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476708 | n.3051C>G | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673786 | p.Ala116Glu | missense_variant | 0.12 |
inhA | 1674586 | p.Ser129Pro | missense_variant | 0.17 |
inhA | 1674838 | p.Ala213Thr | missense_variant | 0.15 |
rpsA | 1834910 | c.1373delA | frameshift_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918088 | p.Thr50Asn | missense_variant | 0.23 |
ndh | 2102211 | p.Ala278Thr | missense_variant | 0.15 |
ndh | 2102617 | p.Asp142Glu | missense_variant | 0.33 |
ndh | 2103024 | p.Pro7Thr | missense_variant | 0.22 |
katG | 2154867 | c.1245G>T | synonymous_variant | 0.13 |
katG | 2156091 | c.21C>A | synonymous_variant | 0.15 |
katG | 2156109 | c.3G>A | synonymous_variant | 0.15 |
PPE35 | 2168696 | c.1917C>A | synonymous_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170620 | c.-8G>C | upstream_gene_variant | 0.17 |
PPE35 | 2170775 | c.-163T>C | upstream_gene_variant | 0.17 |
PPE35 | 2170786 | c.-174G>T | upstream_gene_variant | 0.14 |
Rv1979c | 2222750 | p.Leu139Met | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289910 | c.-669C>A | upstream_gene_variant | 0.17 |
pncA | 2290014 | c.-773T>C | upstream_gene_variant | 0.17 |
kasA | 2517948 | c.-167C>A | upstream_gene_variant | 0.12 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.12 |
kasA | 2519171 | p.Leu353Val | missense_variant | 0.12 |
kasA | 2519280 | p.Pro389Leu | missense_variant | 0.15 |
eis | 2714885 | p.His150Asn | missense_variant | 0.18 |
eis | 2715280 | p.Leu18Pro | missense_variant | 0.14 |
ahpC | 2726630 | p.Phe146Leu | missense_variant | 0.29 |
folC | 2746435 | c.1164C>T | synonymous_variant | 0.13 |
folC | 2747273 | p.Ser109* | stop_gained | 0.14 |
pepQ | 2859678 | c.741A>C | synonymous_variant | 0.15 |
pepQ | 2859936 | c.483C>A | synonymous_variant | 0.12 |
pepQ | 2860600 | c.-182A>C | upstream_gene_variant | 0.18 |
ribD | 2986757 | c.-82C>A | upstream_gene_variant | 0.17 |
ribD | 2987037 | p.Asp67Tyr | missense_variant | 0.25 |
Rv2752c | 3067144 | c.-953G>A | upstream_gene_variant | 0.33 |
thyX | 3068046 | c.-101G>T | upstream_gene_variant | 0.13 |
thyA | 3074161 | p.Pro104Leu | missense_variant | 0.15 |
thyA | 3074199 | c.273G>T | synonymous_variant | 0.17 |
thyA | 3074297 | p.Leu59Met | missense_variant | 0.2 |
ald | 3086656 | c.-164A>T | upstream_gene_variant | 0.5 |
ald | 3087542 | c.723G>T | synonymous_variant | 0.17 |
ald | 3087632 | p.Gln271His | missense_variant | 0.18 |
fbiD | 3339120 | c.3G>T | start_lost | 0.25 |
fbiD | 3339637 | p.Gly174Cys | missense_variant | 0.14 |
fbiD | 3339738 | c.621C>A | synonymous_variant | 0.15 |
fbiD | 3339742 | c.625C>A | synonymous_variant | 0.15 |
fprA | 3473818 | c.-188delA | upstream_gene_variant | 0.13 |
fprA | 3474991 | p.Thr329Ala | missense_variant | 0.15 |
Rv3236c | 3612145 | c.972G>C | synonymous_variant | 0.12 |
Rv3236c | 3612165 | p.Val318Leu | missense_variant | 0.17 |
Rv3236c | 3612196 | c.921C>A | synonymous_variant | 0.25 |
Rv3236c | 3612462 | p.Leu219Met | missense_variant | 0.17 |
Rv3236c | 3613298 | c.-182G>A | upstream_gene_variant | 0.23 |
fbiB | 3640620 | c.-915C>A | upstream_gene_variant | 0.15 |
fbiA | 3641062 | p.Val174Met | missense_variant | 0.17 |
fbiA | 3641093 | p.Ser184Ile | missense_variant | 0.17 |
fbiB | 3641811 | c.277T>C | synonymous_variant | 0.13 |
alr | 3840461 | c.960G>T | synonymous_variant | 0.33 |
alr | 3840627 | p.Ala265Asp | missense_variant | 0.18 |
alr | 3841261 | p.Glu54Lys | missense_variant | 0.14 |
rpoA | 3878036 | p.Glu158* | stop_gained | 0.14 |
ddn | 3986851 | p.Lys3Arg | missense_variant | 0.17 |
ddn | 3986946 | p.Glu35* | stop_gained | 0.13 |
ddn | 3987286 | p.Val148Ala | missense_variant | 0.11 |
clpC1 | 4038394 | p.Arg771Ser | missense_variant | 0.14 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.18 |
clpC1 | 4040358 | p.Gly116Val | missense_variant | 0.22 |
panD | 4044327 | c.-46G>A | upstream_gene_variant | 0.18 |
embC | 4240697 | p.Ala279Ser | missense_variant | 0.18 |
embC | 4240806 | p.Arg315Leu | missense_variant | 0.15 |
embC | 4241054 | p.Pro398Thr | missense_variant | 0.18 |
embC | 4241411 | p.Ile517Leu | missense_variant | 0.13 |
embC | 4242128 | c.2266C>T | synonymous_variant | 0.2 |
embC | 4242366 | p.Ser835Tyr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243776 | p.Gln182Lys | missense_variant | 0.12 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.12 |
embA | 4244538 | p.Ala436Ser | missense_variant | 0.15 |
embA | 4245056 | c.1824C>A | synonymous_variant | 0.14 |
embA | 4245188 | c.1956G>T | synonymous_variant | 0.15 |
embA | 4246218 | p.His996Asn | missense_variant | 0.22 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.43 |
embB | 4247108 | p.Gly199Trp | missense_variant | 0.13 |
embB | 4247821 | c.1308T>C | synonymous_variant | 0.13 |
embB | 4247970 | c.1458dupC | frameshift_variant | 0.12 |
embB | 4247987 | p.Val492Leu | missense_variant | 0.13 |
embB | 4249049 | p.Gly846Cys | missense_variant | 0.33 |
embB | 4249124 | p.Gly871Trp | missense_variant | 0.15 |
embB | 4249265 | p.Pro918Ser | missense_variant | 0.14 |
embB | 4249333 | c.2820C>A | synonymous_variant | 0.15 |
aftB | 4267085 | c.1752G>T | synonymous_variant | 0.22 |
aftB | 4267290 | p.Ala516Val | missense_variant | 0.18 |
aftB | 4267406 | p.Lys477Asn | missense_variant | 0.12 |
aftB | 4267428 | p.Ser470* | stop_gained | 0.17 |
aftB | 4267987 | p.Arg284Ser | missense_variant | 0.5 |
aftB | 4268039 | c.798G>T | synonymous_variant | 0.12 |
aftB | 4268049 | p.Pro263Leu | missense_variant | 0.12 |
aftB | 4268203 | p.Leu212Met | missense_variant | 0.29 |
ethA | 4327532 | c.-59G>T | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |