Run ID: SRR1165643
Sample name:
Date: 03-04-2023 00:56:31
Number of reads: 4726374
Percentage reads mapped: 99.23
Strain: lineage4.3.4.2
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 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.65 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 0.37 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.63 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Leu | missense_variant | 0.63 | rifampicin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.45 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.31 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.3 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289142 | p.Tyr34Asp | missense_variant | 0.18 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 0.18 | ethambutol |
embB | 4247730 | p.Gly406Ala | missense_variant | 0.53 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 0.72 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.66 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490682 | c.-101C>T | upstream_gene_variant | 0.15 |
mshA | 575538 | p.Asp64Gly | missense_variant | 0.67 |
rpoC | 764744 | p.Arg459Trp | missense_variant | 0.61 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.73 |
rpoC | 765494 | p.Val709Leu | missense_variant | 0.61 |
rpoC | 766487 | p.Pro1040Ser | missense_variant | 0.33 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 0.31 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859608 | p.Arg271Gly | missense_variant | 0.29 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 0.39 |
Rv2752c | 3064993 | p.Trp400* | stop_gained | 0.48 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.62 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339287 | p.Arg57Leu | missense_variant | 0.5 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.42 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 0.77 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.29 |
fbiB | 3641358 | c.-177G>T | upstream_gene_variant | 0.25 |
fbiA | 3641439 | c.900_901dupGG | frameshift_variant | 0.18 |
fbiB | 3642294 | c.764_767dupAAGC | frameshift_variant | 0.4 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.66 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.56 |
ubiA | 4269308 | p.Phe176Leu | missense_variant | 0.4 |
ethA | 4326853 | c.612_620dupGCTGCAGCG | disruptive_inframe_insertion | 0.48 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407714 | p.Lys163Asn | missense_variant | 0.55 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.5 |