Run ID: SRR3675531
Sample name:
Date: 04-04-2023 05:32:31
Number of reads: 500497
Percentage reads mapped: 98.38
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 490896 | p.Ser38Arg | missense_variant | 0.22 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.2 |
rpoB | 762184 | p.Gly793Val | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766288 | c.2919C>A | synonymous_variant | 0.18 |
rpoC | 766437 | p.Asp1023Gly | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777935 | c.546C>A | synonymous_variant | 0.18 |
mmpS5 | 778677 | p.Lys77Glu | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800788 | c.-21A>T | upstream_gene_variant | 0.2 |
rplC | 800981 | p.Ser58Ile | missense_variant | 0.18 |
rplC | 801187 | p.Met127Val | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673155 | c.-285G>C | upstream_gene_variant | 0.11 |
rpsA | 1834236 | p.Asp232Gly | missense_variant | 0.18 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.33 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.29 |
rpsA | 1834397 | p.His286Thr | missense_variant | 0.29 |
rpsA | 1834405 | c.864C>G | synonymous_variant | 0.25 |
rpsA | 1834409 | p.Thr290Leu | missense_variant | 0.25 |
rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.25 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.25 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.29 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.4 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.33 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.33 |
rpsA | 1834482 | p.Glu314Gly | missense_variant | 0.33 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.33 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.33 |
rpsA | 1834495 | c.954G>A | synonymous_variant | 0.33 |
rpsA | 1834508 | p.Ile323Val | missense_variant | 0.33 |
rpsA | 1834804 | c.1263C>T | synonymous_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154612 | c.1500G>A | synonymous_variant | 0.25 |
PPE35 | 2167792 | p.Ser941Ala | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.22 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.19 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.52 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.63 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714179 | p.Arg385Gln | missense_variant | 0.14 |
eis | 2715083 | p.Phe84Ile | missense_variant | 0.17 |
folC | 2746443 | p.Asp386Asn | missense_variant | 0.25 |
ribD | 2986872 | p.Thr12Ala | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087504 | p.Val229Ile | missense_variant | 0.11 |
fbiD | 3339692 | p.Pro192His | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840362 | c.1059G>A | synonymous_variant | 0.14 |
alr | 3841369 | c.51delG | frameshift_variant | 0.13 |
rpoA | 3878059 | p.Val150Ala | missense_variant | 0.15 |
clpC1 | 4040662 | p.Leu15Met | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.29 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.21 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.21 |
embB | 4248394 | c.1881G>T | synonymous_variant | 0.13 |
aftB | 4267026 | p.Arg604Leu | missense_variant | 0.22 |
ethA | 4326185 | p.Pro430His | missense_variant | 0.14 |
ethA | 4328046 | c.-573C>A | upstream_gene_variant | 0.29 |
whiB6 | 4338292 | p.Ala77Val | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408298 | c.-96A>G | upstream_gene_variant | 0.22 |