Run ID: SRR7131094
Sample name:
Date: 04-04-2023 18:45:09
Number of reads: 2478334
Percentage reads mapped: 99.99
Strain: lineage4.3.3
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 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.15 | 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 | 8040 | p.Gly247Ser | missense_variant | 0.97 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776724 | p.Tyr586Ser | 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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476354 | n.2699_2700delCT | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476359 | n.2703_2704insGC | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
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 | 0.97 |
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 | 4408156 | p.Leu16Arg | missense_variant | 1.0 |