Run ID: SRR13068977
Sample name:
Date: 03-04-2023 08:12:00
Number of reads: 179285
Percentage reads mapped: 99.42
Strain:
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 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2154100 | p.Ser671* | stop_gained | 0.4 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289186 | p.Leu19Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247574 | p.Asp354Ala | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5896 | c.657C>G | synonymous_variant | 0.67 |
gyrB | 6429 | p.Glu397Val | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 619699 | c.-192G>A | upstream_gene_variant | 0.33 |
ccsA | 620304 | p.Trp138Cys | missense_variant | 0.18 |
rpoC | 764666 | p.Gly433Ser | missense_variant | 1.0 |
rpoC | 765623 | p.Arg752Cys | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777661 | p.Ala274Thr | missense_variant | 0.4 |
mmpL5 | 778137 | p.Arg115Ile | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.4 |
fbiC | 1303058 | p.Glu43Val | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674651 | c.450C>T | synonymous_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2154102 | c.2010C>T | synonymous_variant | 0.4 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289263 | c.-22C>T | upstream_gene_variant | 0.29 |
pncA | 2289601 | c.-360T>G | upstream_gene_variant | 0.2 |
ahpC | 2726039 | c.-154C>A | upstream_gene_variant | 0.33 |
ahpC | 2726423 | c.231C>T | synonymous_variant | 0.5 |
ahpC | 2726737 | p.Asp182Val | missense_variant | 0.29 |
folC | 2746649 | p.Ala317Val | missense_variant | 1.0 |
ribD | 2987368 | p.Val177Gly | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3448641 | c.138C>T | synonymous_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
Rv3236c | 3612696 | p.Arg141Cys | missense_variant | 0.22 |
clpC1 | 4038237 | p.Thr823Asn | missense_variant | 0.17 |
clpC1 | 4039287 | p.Leu473His | missense_variant | 0.29 |
clpC1 | 4039383 | p.Ala441Val | missense_variant | 0.18 |
embC | 4240661 | p.Trp267Arg | missense_variant | 0.15 |
embA | 4243571 | c.339G>A | synonymous_variant | 0.4 |
embA | 4245389 | c.2157C>T | synonymous_variant | 0.2 |
embB | 4247055 | p.Leu181Gln | missense_variant | 0.29 |
embB | 4247223 | p.Trp237* | stop_gained | 0.22 |
aftB | 4267329 | p.Arg503Leu | missense_variant | 0.5 |
aftB | 4269690 | c.-854C>T | upstream_gene_variant | 0.33 |
ubiA | 4269811 | c.22delC | frameshift_variant | 0.33 |
ethA | 4327208 | p.Ala89Val | missense_variant | 0.2 |
ethA | 4327247 | p.Ala76Asp | missense_variant | 1.0 |
ethR | 4327282 | c.-267G>A | upstream_gene_variant | 0.18 |
ethA | 4327361 | p.Arg38Leu | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |