Run ID: SRR7535080
Sample name:
Date: 04-04-2023 19:44:25
Number of reads: 2435480
Percentage reads mapped: 9.78
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155692 | p.Ser140Asn | missense_variant | 0.28 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5078 | c.-162_-161insG | upstream_gene_variant | 1.0 |
gyrB | 6815 | p.Lys526Gln | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576210 | p.Ala288Asp | missense_variant | 0.12 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.16 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.38 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.34 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.35 |
rpoC | 762932 | c.-438G>T | upstream_gene_variant | 0.35 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.32 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.31 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.33 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.37 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.36 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.28 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.13 |
rpoC | 764705 | c.1336C>T | synonymous_variant | 0.12 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.13 |
rpoC | 766628 | c.3262dupG | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775855 | p.Gly876Ser | 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 | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472648 | n.803G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472824 | n.979T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472956 | n.1111T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473204 | n.1359C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474221 | n.564T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475787 | n.2130C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.21 |
fabG1 | 1673312 | c.-128C>A | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155668 | c.444G>C | synonymous_variant | 0.24 |
katG | 2155674 | c.438G>C | synonymous_variant | 0.24 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.28 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.25 |
PPE35 | 2170049 | c.564G>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859607 | p.Arg271Leu | missense_variant | 0.11 |
pepQ | 2859983 | p.Ala146Ser | missense_variant | 0.11 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.17 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |