Run ID: SRR6045064
Sample name:
Date: 04-04-2023 11:52:12
Number of reads: 1327691
Percentage reads mapped: 70.83
Strain: lineage4.3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.1 | Euro-American (LAM) | LAM9 | None | 0.99 |
lineage4.3.1.1 | Euro-American (LAM) | LAM9 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.97 | streptomycin |
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 | 9683 | c.2382G>A | synonymous_variant | 0.11 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.28 |
fgd1 | 491380 | p.Glu200* | stop_gained | 0.12 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.2 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.28 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407405 | c.-65C>A | upstream_gene_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471660 | n.-186G>A | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472141 | n.296G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472806 | n.961A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473034 | n.1189A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473751 | n.94C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.43 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169090 | p.Val508Glu | missense_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.11 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.15 |
PPE35 | 2169985 | p.Ala210Thr | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518407 | p.Ala98Val | missense_variant | 0.12 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.32 |
thyX | 3067966 | c.-21G>A | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074654 | c.-183T>G | upstream_gene_variant | 0.23 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.13 |
Rv3083 | 3449236 | p.Arg245Gly | missense_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethR | 4327738 | p.Tyr64His | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |