Run ID: SRR4034064
Sample name:
Date: 04-04-2023 06:33:05
Number of reads: 685756
Percentage reads mapped: 99.61
Strain: lineage4.3.2.1
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 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 7184 | p.Ser649Pro | missense_variant | 0.12 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7995 | p.Gly232* | stop_gained | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 762471 | p.Ile889Val | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765046 | p.Met559Ile | missense_variant | 0.1 |
rpoC | 766048 | c.2679C>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778191 | p.Gly97Val | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800658 | c.-151T>C | upstream_gene_variant | 0.11 |
fbiC | 1303172 | p.Arg81Met | missense_variant | 0.13 |
fbiC | 1303536 | c.606G>C | synonymous_variant | 1.0 |
Rv1258c | 1406605 | c.736C>T | synonymous_variant | 0.13 |
embR | 1417175 | p.Ala58Asp | missense_variant | 0.25 |
embR | 1417369 | c.-22C>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472612 | n.767G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476164 | n.2509G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476583 | n.2926G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673246 | c.-194G>T | upstream_gene_variant | 0.12 |
fabG1 | 1673452 | p.Ala5Ser | missense_variant | 0.17 |
inhA | 1674075 | c.-127C>G | upstream_gene_variant | 0.14 |
inhA | 1674670 | p.Ala157Thr | missense_variant | 0.29 |
tlyA | 1917953 | p.Ala5Asp | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918479 | c.540G>T | synonymous_variant | 0.2 |
tlyA | 1918542 | c.603G>A | synonymous_variant | 0.25 |
tlyA | 1918638 | c.699A>C | synonymous_variant | 0.33 |
katG | 2154193 | p.Arg640His | missense_variant | 0.29 |
katG | 2154879 | c.1233C>A | synonymous_variant | 0.12 |
katG | 2156423 | c.-312A>G | upstream_gene_variant | 0.12 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.13 |
Rv1979c | 2223072 | c.93T>C | synonymous_variant | 0.14 |
Rv1979c | 2223206 | c.-42T>C | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289371 | c.-130C>A | upstream_gene_variant | 0.14 |
pncA | 2289447 | c.-206G>T | upstream_gene_variant | 0.11 |
pncA | 2289877 | c.-636C>A | upstream_gene_variant | 0.2 |
pncA | 2290107 | c.-866T>A | upstream_gene_variant | 1.0 |
pncA | 2290237 | c.-996G>T | upstream_gene_variant | 0.13 |
folC | 2747320 | c.279C>A | synonymous_variant | 0.25 |
pepQ | 2859434 | p.Tyr329His | missense_variant | 0.17 |
ribD | 2986805 | c.-34G>T | upstream_gene_variant | 0.14 |
ribD | 2986850 | c.12T>C | synonymous_variant | 0.11 |
Rv2752c | 3064564 | c.1627delG | frameshift_variant | 0.17 |
Rv2752c | 3065394 | p.Met266Ile | missense_variant | 0.15 |
Rv2752c | 3065687 | p.Gly169Ser | missense_variant | 0.14 |
Rv2752c | 3065892 | c.300C>A | synonymous_variant | 0.14 |
Rv2752c | 3066302 | c.-111C>G | upstream_gene_variant | 0.1 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086925 | p.Gln36Lys | missense_variant | 0.11 |
Rv3083 | 3448798 | p.His99Asn | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568726 | c.-47C>A | upstream_gene_variant | 0.15 |
Rv3236c | 3612213 | p.Ala302Thr | missense_variant | 0.13 |
fbiB | 3641610 | p.Gly26Cys | missense_variant | 0.13 |
alr | 3841603 | c.-183C>A | upstream_gene_variant | 0.12 |
ddn | 3986869 | p.Leu9Arg | missense_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039486 | p.Gly407Ser | missense_variant | 0.33 |
panD | 4044171 | p.Asp37Glu | missense_variant | 0.15 |
embC | 4240250 | p.Leu130Met | missense_variant | 0.22 |
embC | 4240911 | p.Ala350Glu | missense_variant | 0.17 |
embC | 4242028 | c.2166G>A | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246339 | p.Leu1036Pro | missense_variant | 0.15 |
embB | 4248073 | c.1560C>T | synonymous_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |