Run ID: ERR4817024
Sample name:
Date: 01-04-2023 14:45:41
Number of reads: 897415
Percentage reads mapped: 99.59
Strain: lineage4.6.5
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.5 | Euro-American | T;LAM | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
tlyA | 1918647 | p.Asn236Lys | missense_variant | 1.0 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5489 | p.Ile84Val | missense_variant | 1.0 |
gyrB | 5813 | p.Arg192Ser | missense_variant | 0.13 |
gyrB | 7031 | p.Gly598Trp | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8033 | p.Tyr244* | stop_gained | 0.25 |
gyrA | 8300 | c.999G>A | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.9 |
fgd1 | 491395 | p.Glu205Gln | missense_variant | 0.12 |
mshA | 575521 | c.174A>C | synonymous_variant | 0.12 |
mshA | 575527 | c.180G>C | synonymous_variant | 0.12 |
mshA | 575536 | c.189T>C | synonymous_variant | 0.15 |
mshA | 575542 | c.195C>G | synonymous_variant | 0.15 |
mshA | 575561 | p.Met72Val | missense_variant | 0.12 |
mshA | 575569 | c.222A>G | synonymous_variant | 0.15 |
mshA | 575571 | p.Ser75Thr | missense_variant | 0.17 |
mshA | 575576 | c.229C>T | synonymous_variant | 0.17 |
mshA | 575587 | c.240C>G | synonymous_variant | 0.14 |
mshA | 575590 | c.243T>G | synonymous_variant | 0.14 |
mshA | 575617 | c.270C>G | synonymous_variant | 0.15 |
mshA | 576369 | p.Arg341Leu | missense_variant | 0.14 |
ccsA | 620216 | p.Asn109Ser | missense_variant | 0.11 |
rpoB | 759715 | c.-92G>A | upstream_gene_variant | 0.17 |
rpoB | 760082 | c.276C>T | synonymous_variant | 0.1 |
rpoB | 760106 | c.300G>T | synonymous_variant | 0.12 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.11 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.1 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.13 |
rpoB | 761717 | c.1911C>G | synonymous_variant | 0.2 |
rpoB | 761959 | p.Met718Lys | missense_variant | 0.11 |
rpoB | 762199 | p.Gly798Ala | missense_variant | 0.11 |
rpoB | 762429 | p.Asp875Tyr | missense_variant | 0.14 |
rpoB | 762455 | p.His883Gln | missense_variant | 0.14 |
rpoC | 764672 | p.Gln435* | stop_gained | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777974 | c.507C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304635 | p.Gln569Lys | missense_variant | 0.12 |
fbiC | 1304932 | p.Ala668Ser | missense_variant | 0.11 |
atpE | 1461008 | c.-37G>A | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673970 | c.-232C>T | upstream_gene_variant | 0.12 |
inhA | 1674545 | p.Asp115Val | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918220 | p.Gly94Val | missense_variant | 0.12 |
ndh | 2102943 | p.Lys34Glu | missense_variant | 0.11 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.13 |
PPE35 | 2170469 | c.144G>T | synonymous_variant | 0.17 |
Rv1979c | 2222166 | c.999C>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.12 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.12 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.12 |
kasA | 2518896 | c.783_784delGT | frameshift_variant | 0.12 |
kasA | 2519169 | p.Ala352Glu | missense_variant | 0.17 |
kasA | 2519244 | p.Asp377Gly | missense_variant | 0.29 |
eis | 2715038 | p.Ala99Ser | missense_variant | 0.11 |
folC | 2746362 | p.Asp413Tyr | missense_variant | 0.13 |
folC | 2746934 | p.Arg222Pro | missense_variant | 0.15 |
folC | 2746995 | p.Val202Ile | missense_variant | 1.0 |
ribD | 2987146 | p.Arg103His | missense_variant | 0.12 |
thyX | 3067714 | p.Val78Met | missense_variant | 0.12 |
thyA | 3074028 | c.444G>C | synonymous_variant | 0.15 |
Rv3083 | 3449868 | c.1365C>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612537 | p.Gly194Arg | missense_variant | 0.13 |
fbiA | 3640346 | c.-196delA | upstream_gene_variant | 1.0 |
fbiA | 3640954 | p.Pro138Ala | missense_variant | 0.14 |
fbiB | 3640965 | c.-570C>G | upstream_gene_variant | 0.13 |
fbiB | 3640974 | c.-561T>C | upstream_gene_variant | 0.13 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.13 |
clpC1 | 4038332 | c.2373C>T | synonymous_variant | 1.0 |
panD | 4044088 | p.Gly65Asp | missense_variant | 0.11 |
embC | 4242588 | p.Gly909Glu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245071 | c.1839G>A | synonymous_variant | 0.13 |
embB | 4248894 | p.Pro794Gln | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |