Run ID: SRR6807688
Sample name:
Date: 04-04-2023 16:21:13
Number of reads: 1813907
Percentage reads mapped: 91.13
Strain: lineage4.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94His | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.21 | streptomycin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289213 | p.Gln10Pro | missense_variant | 0.98 | pyrazinamide |
eis | 2715342 | c.-10G>A | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
ethA | 4326014 | c.-2503_1459del | frameshift_variant&start_lost | 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 | 491247 | c.465C>T | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.34 |
ccsA | 619969 | p.Val27Ile | missense_variant | 1.0 |
rpoC | 764888 | p.Leu507Val | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304253 | c.1323G>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472669 | n.824_825insTGGA | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475752 | n.2095C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475776 | n.2119G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.21 |
Rv3083 | 3448593 | c.92_93dupCA | frameshift_variant | 0.9 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |