Run ID: SRR19428574
Sample name:
Date: 03-04-2023 21:40:37
Number of reads: 679691
Percentage reads mapped: 99.29
Strain: lineage4.3.4.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5566 | p.Phe109Leu | missense_variant | 0.12 |
gyrB | 5610 | p.Gly124Asp | missense_variant | 0.12 |
gyrB | 5701 | c.466dupC | frameshift_variant | 0.13 |
gyrB | 6266 | p.Pro343Thr | missense_variant | 0.14 |
gyrA | 6817 | c.-485G>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7524 | p.Arg75Trp | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.94 |
rpoB | 761573 | c.1767C>T | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777280 | p.Ala401Ser | missense_variant | 0.14 |
mmpL5 | 777613 | p.Gly290Trp | missense_variant | 0.12 |
mmpL5 | 778973 | c.-493T>C | upstream_gene_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.38 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472667 | n.822T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472769 | n.924C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473316 | n.1471C>A | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833454 | c.-88G>T | upstream_gene_variant | 0.12 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102592 | c.449_450dupGC | frameshift_variant | 0.12 |
katG | 2154084 | c.2028G>T | synonymous_variant | 0.2 |
katG | 2154731 | p.Gln461Glu | missense_variant | 0.13 |
PPE35 | 2167760 | c.2853G>T | synonymous_variant | 0.13 |
PPE35 | 2168204 | c.2409G>A | synonymous_variant | 0.13 |
PPE35 | 2168233 | p.Ile794Val | missense_variant | 0.18 |
PPE35 | 2169158 | p.Leu485Phe | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518771 | c.657C>A | synonymous_variant | 0.13 |
folC | 2747585 | p.Asn5Ser | missense_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074363 | p.Asp37Tyr | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449147 | p.Ser215Trp | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3612546 | p.Ala191Ser | missense_variant | 0.14 |
Rv3236c | 3612905 | p.Leu71Ser | missense_variant | 0.11 |
Rv3236c | 3612970 | p.Leu49Phe | missense_variant | 0.13 |
alr | 3840296 | c.1125G>A | synonymous_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
panD | 4044228 | c.54C>T | synonymous_variant | 0.12 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 1.0 |
embC | 4241443 | c.1581C>T | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.1 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.14 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.14 |
embB | 4249491 | p.Ala993Val | missense_variant | 0.12 |
embB | 4249669 | c.3156C>T | synonymous_variant | 0.12 |
ethA | 4327233 | p.Ile81Val | missense_variant | 0.1 |
whiB6 | 4338333 | c.189A>G | synonymous_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
fbiC | 1305494 | c.2565_*56delCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |