Run ID: SRR5535692
Sample name:
Date: 04-04-2023 10:37:51
Number of reads: 837241
Percentage reads mapped: 99.13
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326831 | p.Gln215* | stop_gained | 0.2 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5167 | c.-73C>A | upstream_gene_variant | 0.67 |
gyrB | 5963 | p.Ala242Ser | missense_variant | 0.25 |
gyrB | 6864 | p.Thr542Lys | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7396 | p.Ala32Val | missense_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8011 | p.Ser237Tyr | missense_variant | 0.4 |
gyrA | 8109 | p.Val270Leu | missense_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9332 | p.Asn677Lys | missense_variant | 0.2 |
fgd1 | 491271 | c.489C>T | synonymous_variant | 0.29 |
mshA | 575314 | c.-34C>A | upstream_gene_variant | 0.22 |
mshA | 575420 | p.Thr25Ser | missense_variant | 0.25 |
mshA | 576404 | p.Glu353* | stop_gained | 0.29 |
ccsA | 620286 | c.396G>T | synonymous_variant | 0.67 |
rpoB | 760585 | p.Asn260Ser | missense_variant | 0.12 |
rpoB | 761526 | p.Asp574Asn | missense_variant | 0.29 |
rpoB | 761787 | c.1981C>A | synonymous_variant | 0.25 |
rpoC | 763136 | c.-234C>A | upstream_gene_variant | 0.29 |
rpoC | 764810 | p.Pro481Thr | missense_variant | 0.18 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765337 | p.Trp656Cys | missense_variant | 0.14 |
rpoC | 765515 | p.Leu716Ile | missense_variant | 0.29 |
rpoC | 765784 | c.2415C>A | synonymous_variant | 0.22 |
rpoC | 765808 | p.Gln813His | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778382 | c.-608C>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781763 | c.204C>T | synonymous_variant | 0.25 |
rplC | 801102 | c.294G>C | synonymous_variant | 0.33 |
rplC | 801318 | p.Met170Ile | missense_variant | 0.5 |
fbiC | 1303247 | p.Thr106Met | missense_variant | 0.13 |
fbiC | 1303508 | p.Pro193Gln | missense_variant | 0.33 |
fbiC | 1303767 | p.Lys279Asn | missense_variant | 0.67 |
fbiC | 1304220 | c.1290G>T | synonymous_variant | 0.29 |
fbiC | 1305306 | c.2376A>G | synonymous_variant | 0.25 |
Rv1258c | 1406834 | c.507C>A | synonymous_variant | 0.33 |
embR | 1417140 | p.Ala70Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475193 | n.1536C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475962 | n.2305G>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 1.0 |
inhA | 1673586 | c.-616C>A | upstream_gene_variant | 0.25 |
inhA | 1674460 | p.Lys87Gln | missense_variant | 0.25 |
inhA | 1674770 | p.Ala190Asp | missense_variant | 0.22 |
inhA | 1674833 | p.Ala211Asp | missense_variant | 0.29 |
rpsA | 1833409 | c.-133C>A | upstream_gene_variant | 0.22 |
rpsA | 1833664 | c.123C>T | synonymous_variant | 0.5 |
rpsA | 1834362 | p.Leu274Ser | missense_variant | 0.4 |
tlyA | 1917823 | c.-117C>A | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917990 | c.51G>T | synonymous_variant | 0.25 |
ndh | 2101880 | p.Ser388Ile | missense_variant | 0.33 |
katG | 2155958 | p.Pro52Thr | missense_variant | 0.13 |
katG | 2156344 | c.-233C>A | upstream_gene_variant | 0.4 |
PPE35 | 2168499 | p.Ser705* | stop_gained | 1.0 |
PPE35 | 2168558 | c.2055C>A | synonymous_variant | 0.4 |
PPE35 | 2170319 | p.Glu98Asp | missense_variant | 0.5 |
PPE35 | 2170355 | c.258G>T | synonymous_variant | 0.67 |
pncA | 2289432 | c.-191C>A | upstream_gene_variant | 0.14 |
pncA | 2289633 | c.-392G>T | upstream_gene_variant | 0.33 |
eis | 2714309 | p.Pro342Thr | missense_variant | 0.67 |
eis | 2714444 | p.Arg297Ser | missense_variant | 0.18 |
eis | 2714829 | c.504C>A | synonymous_variant | 0.25 |
eis | 2715049 | p.Gly95Asp | missense_variant | 0.18 |
folC | 2746767 | p.Gln278Glu | missense_variant | 1.0 |
folC | 2747022 | p.Val193Ile | missense_variant | 1.0 |
folC | 2747780 | c.-182C>T | upstream_gene_variant | 0.33 |
pepQ | 2859647 | p.Gln258Lys | missense_variant | 0.4 |
pepQ | 2860151 | p.Ala90Thr | missense_variant | 0.22 |
ribD | 2987420 | c.582C>T | synonymous_variant | 0.14 |
Rv2752c | 3064527 | c.1665C>A | synonymous_variant | 0.4 |
Rv2752c | 3064878 | c.1314C>A | synonymous_variant | 0.25 |
Rv2752c | 3064944 | c.1248G>T | synonymous_variant | 0.25 |
Rv2752c | 3065278 | p.Thr305Ile | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339457 | p.Gln114* | stop_gained | 0.5 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 1.0 |
Rv3083 | 3448924 | p.Gly141Cys | missense_variant | 0.5 |
Rv3083 | 3449342 | p.Ser280Phe | missense_variant | 0.29 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474319 | p.Gly105Cys | missense_variant | 0.4 |
fprA | 3474433 | p.Pro143Thr | missense_variant | 0.5 |
fprA | 3474619 | p.Ala205Ser | missense_variant | 0.17 |
fprA | 3474712 | p.Glu236* | stop_gained | 0.29 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 1.0 |
fbiB | 3642597 | p.Asp355Tyr | missense_variant | 0.2 |
rpoA | 3878130 | c.378C>A | synonymous_variant | 0.25 |
rpoA | 3878149 | p.Asn120Thr | missense_variant | 0.2 |
rpoA | 3878304 | c.204G>T | synonymous_variant | 0.29 |
clpC1 | 4038230 | p.Lys825Asn | missense_variant | 0.25 |
clpC1 | 4038337 | p.Leu790Ile | missense_variant | 0.17 |
clpC1 | 4039927 | p.Arg260Cys | missense_variant | 0.25 |
panD | 4044223 | p.Leu20Arg | missense_variant | 0.22 |
embC | 4240068 | p.Ser69Ile | missense_variant | 0.2 |
embC | 4240359 | p.Ala166Asp | missense_variant | 0.33 |
embC | 4241415 | p.Arg518His | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242665 | p.Ala935Ser | missense_variant | 0.2 |
embC | 4242672 | p.Pro937Gln | missense_variant | 0.22 |
embA | 4245352 | p.Lys707Met | missense_variant | 0.5 |
embA | 4246236 | p.Leu1002Ile | missense_variant | 0.5 |
embB | 4246584 | p.Arg24Leu | missense_variant | 0.33 |
embB | 4246586 | p.Gly25Trp | missense_variant | 0.33 |
embB | 4247807 | p.Ala432Ser | missense_variant | 0.25 |
embB | 4248122 | p.Leu537Met | missense_variant | 0.25 |
embB | 4249024 | c.2511C>A | synonymous_variant | 0.29 |
aftB | 4267131 | p.Pro569Leu | missense_variant | 1.0 |
ubiA | 4269238 | p.Ala199Asp | missense_variant | 0.4 |
ubiA | 4269541 | p.Pro98His | missense_variant | 0.29 |
ubiA | 4269623 | p.Leu71Ile | missense_variant | 0.2 |
ubiA | 4269713 | p.Gly41Arg | missense_variant | 0.22 |
ethA | 4326075 | p.Leu467Ile | missense_variant | 0.2 |
ethA | 4326896 | p.Ala193Glu | missense_variant | 0.2 |
ethA | 4327206 | p.Ala90Thr | missense_variant | 0.67 |
ethA | 4327475 | c.-2C>A | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338674 | c.-153G>A | upstream_gene_variant | 1.0 |