Run ID: SRR1196557
Sample name:
Date: 03-04-2023 05:28:50
Number of reads: 83439
Percentage reads mapped: 3.49
Strain: lineage4.9;lineage2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.05 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.95 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.09 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.95 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7030 | c.1792_1794delGGG | conservative_inframe_deletion | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776332 | c.2149C>A | synonymous_variant | 0.5 |
mmpL5 | 776362 | p.Gln707* | stop_gained | 0.4 |
mmpL5 | 776384 | c.2097C>T | synonymous_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.75 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
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 | 0.98 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475574 | n.1917C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.5 |
katG | 2156218 | c.-107G>T | upstream_gene_variant | 0.29 |
PPE35 | 2168311 | p.Gln768* | stop_gained | 1.0 |
PPE35 | 2169914 | c.699C>A | synonymous_variant | 0.67 |
PPE35 | 2169919 | p.Leu232Ile | missense_variant | 0.67 |
Rv1979c | 2222136 | p.Lys343Asn | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
folC | 2747142 | p.Glu153* | stop_gained | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242999 | p.Ala1046Val | missense_variant | 0.67 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245287 | c.2055G>A | synonymous_variant | 0.4 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |