Run ID: SRR10315473
Sample name:
Date: 02-04-2023 17:06:47
Number of reads: 5808369
Percentage reads mapped: 88.68
Strain: lineage4.8.1
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
lineage4.8.1 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 0.97 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288790 | p.Leu151Ser | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326213 | p.Arg421* | stop_gained | 0.17 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.25 |
rpoB | 759691 | c.-116A>T | upstream_gene_variant | 0.11 |
rpoB | 760005 | p.Ser67Pro | missense_variant | 0.11 |
rpoC | 763384 | p.Asn5Lys | missense_variant | 0.17 |
rpoC | 763474 | p.Asn35Lys | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776384 | c.2097C>T | synonymous_variant | 0.12 |
mmpL5 | 776785 | p.Glu566* | stop_gained | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800664 | c.-145G>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471975 | n.130G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472968 | n.1123C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473017 | n.1172A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473022 | n.1177G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473749 | n.92A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474169 | n.512A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474339 | n.682C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476404 | n.2747G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476474 | n.2817C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1834272 | p.His244Leu | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102662 | c.381C>G | synonymous_variant | 0.12 |
katG | 2154150 | c.1962C>A | synonymous_variant | 0.12 |
katG | 2156015 | p.Gly33Ser | missense_variant | 0.13 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168521 | p.Gln698Lys | missense_variant | 0.18 |
PPE35 | 2169431 | c.1182G>A | synonymous_variant | 0.15 |
PPE35 | 2169943 | p.Leu224Phe | missense_variant | 0.11 |
Rv1979c | 2222118 | c.1047G>T | synonymous_variant | 0.14 |
Rv1979c | 2223143 | p.Gly8* | stop_gained | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3074138 | p.Ile112Phe | missense_variant | 0.11 |
ald | 3086756 | c.-64A>T | upstream_gene_variant | 0.11 |
ald | 3086876 | c.57C>T | synonymous_variant | 0.17 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 1.0 |
whiB7 | 3568646 | c.33delC | frameshift_variant | 0.11 |
fbiB | 3642874 | p.Leu447Arg | missense_variant | 1.0 |
clpC1 | 4038650 | c.2055C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267312 | p.Gly509Trp | missense_variant | 0.13 |
ethR | 4326565 | c.-984C>A | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |