Run ID: SRR13861566
Sample name:
Date: 03-04-2023 09:34:58
Number of reads: 605041
Percentage reads mapped: 15.14
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6715 | c.-587C>T | upstream_gene_variant | 1.0 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.15 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.15 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.16 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.16 |
gyrA | 9062 | c.1761C>G | synonymous_variant | 0.14 |
fgd1 | 490833 | c.51G>A | synonymous_variant | 0.15 |
fgd1 | 490842 | c.60C>G | synonymous_variant | 0.17 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.15 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.12 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.13 |
fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.13 |
mshA | 575693 | p.Pro116Ala | missense_variant | 0.95 |
rpoB | 759863 | p.Gln19His | missense_variant | 1.0 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760399 | p.Val198Ala | missense_variant | 1.0 |
rpoB | 760565 | c.759A>G | synonymous_variant | 0.15 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.17 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.22 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.19 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.17 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.22 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.21 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.2 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.21 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.2 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.22 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.22 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.25 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.24 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.29 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.21 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.21 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.21 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.15 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.15 |
rpoB | 760776 | p.Ser324Thr | missense_variant | 0.15 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.19 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.17 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.22 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.17 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.14 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.13 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.13 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.19 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.15 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.14 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.14 |
rpoB | 761094 | c.1288C>T | synonymous_variant | 0.21 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.21 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.22 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.19 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.2 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.17 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.18 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.19 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.17 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.16 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.13 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.13 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.14 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.16 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.16 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.14 |
rpoB | 763150 | p.Phe1115Tyr | missense_variant | 1.0 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.14 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.14 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.14 |
rpoC | 763658 | p.Leu97Phe | missense_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.16 |
rpoC | 763708 | c.339G>A | synonymous_variant | 0.15 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.14 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.15 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.15 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.16 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.17 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.15 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.14 |
rpoC | 764516 | p.Asp383Asn | missense_variant | 0.88 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.15 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.16 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.17 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.16 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.16 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.16 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.16 |
rpoC | 766103 | p.Arg912Gly | missense_variant | 0.88 |
mmpL5 | 775834 | p.Ala883Ser | missense_variant | 0.16 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.14 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.14 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.15 |
mmpL5 | 777066 | p.Ile472Ser | missense_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.18 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.18 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.15 |
rplC | 801228 | c.420T>C | synonymous_variant | 0.15 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.14 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.13 |
fbiC | 1305297 | c.2367G>C | synonymous_variant | 0.14 |
fbiC | 1305300 | c.2370A>G | synonymous_variant | 0.14 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.14 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.14 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.14 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.14 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.82 |
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 | 0.83 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.94 |
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 | 0.95 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834097 | p.Ser186Thr | missense_variant | 0.14 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.15 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.12 |
rpsA | 1834623 | p.Ser361Trp | missense_variant | 0.16 |
ndh | 2103185 | c.-143A>C | upstream_gene_variant | 1.0 |
PPE35 | 2168894 | c.1718dupG | frameshift_variant | 1.0 |
PPE35 | 2170039 | p.Ala192Thr | missense_variant | 1.0 |
Rv1979c | 2221777 | p.Ala463Val | missense_variant | 1.0 |
kasA | 2518793 | p.Ser227Thr | missense_variant | 1.0 |
kasA | 2519068 | c.954C>T | synonymous_variant | 0.17 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.14 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.14 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.14 |
ahpC | 2726300 | c.108C>A | synonymous_variant | 0.95 |
folC | 2747094 | p.Asp169His | missense_variant | 1.0 |
Rv2752c | 3064936 | p.Ser419* | stop_gained | 1.0 |
Rv2752c | 3065523 | c.669C>T | synonymous_variant | 0.94 |
Rv2752c | 3066039 | c.153C>T | synonymous_variant | 1.0 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.14 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.15 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.21 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.19 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.17 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.17 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.17 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.15 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.15 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.15 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.14 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.14 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.17 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.14 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.14 |
thyA | 3074199 | c.273G>A | synonymous_variant | 0.13 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.12 |
alr | 3841286 | c.135T>A | synonymous_variant | 1.0 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.19 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.21 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.2 |
rpoA | 3877899 | p.Ser203Arg | missense_variant | 0.13 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.22 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.22 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.24 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.24 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.24 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.17 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.18 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.17 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.18 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.19 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.19 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.19 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.21 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.19 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.19 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.19 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.19 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.17 |
clpC1 | 4038748 | p.Arg653Cys | missense_variant | 0.13 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.13 |
clpC1 | 4039368 | p.Lys446Thr | missense_variant | 1.0 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.13 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.21 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.21 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.21 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.21 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.25 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.25 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.25 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.19 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.19 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.17 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.17 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.2 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.21 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.23 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.14 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.2 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.19 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.17 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.14 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.14 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.16 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.15 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.21 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.19 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.19 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.19 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.18 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.18 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.18 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.14 |
embC | 4241777 | p.Gly639Ser | missense_variant | 0.93 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.14 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.21 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.21 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.21 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.23 |
embB | 4247536 | c.1023C>G | synonymous_variant | 0.18 |
embB | 4247629 | c.1116C>G | synonymous_variant | 0.18 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.16 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.15 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.15 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.16 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.21 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.21 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.19 |
embB | 4249268 | p.Asp919Tyr | missense_variant | 0.17 |
embB | 4249276 | c.2763A>G | synonymous_variant | 0.17 |
embB | 4249282 | c.2769A>C | synonymous_variant | 0.18 |
embB | 4249297 | c.2784G>C | synonymous_variant | 0.17 |
aftB | 4269075 | c.-239T>C | upstream_gene_variant | 0.14 |
ubiA | 4269088 | p.Ala249Val | missense_variant | 0.13 |
ubiA | 4269104 | p.Ser244Gly | missense_variant | 0.14 |
ubiA | 4269106 | c.727delT | frameshift_variant | 0.14 |
ubiA | 4269117 | p.Glu239Asp | missense_variant | 0.14 |
ubiA | 4269141 | p.Leu231Val | missense_variant | 0.14 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.14 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.14 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.15 |
ubiA | 4269888 | c.-55C>A | upstream_gene_variant | 1.0 |