Run ID: SRR1049622
Sample name:
Date: 02-04-2023 18:04:40
Number of reads: 2526471
Percentage reads mapped: 65.63
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288850 | c.390_391dupGG | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5195 | c.-45C>G | upstream_gene_variant | 0.97 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.12 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.12 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.12 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.12 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.12 |
rpoB | 762938 | c.3133_3136delATGA | frameshift_variant | 0.12 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.1 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.11 |
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 | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472826 | n.981G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.96 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746923 | p.Gly226Ser | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.96 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243692 | p.Gly154Ser | missense_variant | 1.0 |
embB | 4246904 | p.Val131Met | missense_variant | 1.0 |
ethA | 4328252 | c.-779T>G | upstream_gene_variant | 0.95 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407758 | p.Ser149Arg | missense_variant | 0.99 |