Run ID: SRR1184379
Sample name:
Date: 03-04-2023 05:20:58
Number of reads: 133289
Percentage reads mapped: 6.41
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 0.67 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.91 | streptomycin |
alr | 3841083 | p.Leu113Arg | missense_variant | 0.67 | cycloserine |
embB | 4247431 | p.Met306Ile | missense_variant | 0.67 | ethambutol |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.75 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763582 | p.Lys71Asn | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775753 | p.Ile910Val | missense_variant | 0.4 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776176 | c.2304delG | frameshift_variant | 0.4 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302957 | c.27C>T | synonymous_variant | 0.4 |
fbiC | 1305455 | p.Arg842His | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472070 | n.225G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.57 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169714 | p.Gly300Val | missense_variant | 0.22 |
PPE35 | 2169896 | c.717C>T | synonymous_variant | 0.18 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726191 | c.-2T>A | upstream_gene_variant | 0.67 |
folC | 2746248 | p.Ala451Thr | missense_variant | 0.67 |
ribD | 2987175 | p.Glu113* | stop_gained | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840402 | p.Arg340Leu | missense_variant | 0.29 |
embB | 4248442 | c.1929C>T | synonymous_variant | 0.33 |
aftB | 4268258 | c.579C>T | synonymous_variant | 0.4 |
ethA | 4326517 | c.957G>A | synonymous_variant | 0.4 |
ethA | 4326692 | p.Arg261Gln | missense_variant | 1.0 |
ethA | 4328301 | c.-828C>T | upstream_gene_variant | 0.25 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |