Run ID: ERR6197037
Sample name:
Date: 02-04-2023 01:50:02
Number of reads: 2201238
Percentage reads mapped: 96.65
Strain: lineage4.3.4.2
Drug-resistance: MDR-TB
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 | 0.99 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.95 | rifampicin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.84 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.82 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288852 | c.375_389delCGATGAGGTCGATGT | disruptive_inframe_deletion | 0.98 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.17 |
rpoC | 764918 | p.Val517Leu | missense_variant | 1.0 |
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 | 1406213 | c.1128G>A | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476262 | n.2605G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833469 | c.-73G>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.96 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407970 | p.Pro78Leu | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |