Run ID: SRR6045110
Sample name:
Date: 04-04-2023 11:53:03
Number of reads: 1789645
Percentage reads mapped: 81.22
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 | 8056 | p.Arg252Leu | missense_variant | 0.98 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.23 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.98 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474029 | n.372G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474208 | n.551C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474213 | n.556G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475552 | n.1895G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475574 | n.1917C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475760 | n.2103C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476090 | n.2433C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.12 |
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 | 2170048 | p.Leu189Val | missense_variant | 0.18 |
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 | 2726012 | c.-181T>C | 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 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |