Run ID: SRR6046761
Sample name:
Date: 04-04-2023 12:22:54
Number of reads: 1492405
Percentage reads mapped: 91.57
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 0.96 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472222 | n.377G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472229 | n.384C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474199 | n.542G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475717 | n.2060C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.45 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 1.0 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.18 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245303 | c.2071C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |