Run ID: ERR987734
Sample name:
Date: 02-04-2023 13:22:18
Number of reads: 1633121
Percentage reads mapped: 92.77
Strain: lineage4.3.4.2
Drug-resistance: HR-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 | 1.0 |
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 |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
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 | 762101 | c.2295C>T | synonymous_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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472339 | n.494C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472607 | n.762G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472608 | n.763T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472615 | n.770C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472620 | n.775A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472634 | n.789T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472639 | n.794G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472643 | n.798A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472644 | n.799C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474187 | n.530T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475869 | n.2212C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476246 | n.2589G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476353 | n.2696G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.55 |
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 | 0.47 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476513 | n.2856G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476545 | n.2888C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476565 | n.2908G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476566 | n.2909A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476577 | n.2920T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476578 | n.2921C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476592 | n.2935G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.17 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
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 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328019 | c.-546G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338593 | c.-73delT | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>C | upstream_gene_variant | 1.0 |
gid | 4407980 | p.Pro75Ala | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |