Run ID: SRR5535704
Sample name:
Date: 04-04-2023 10:38:32
Number of reads: 923091
Percentage reads mapped: 99.46
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288751 | p.Ser164* | stop_gained | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5188 | c.-52C>A | upstream_gene_variant | 0.33 |
gyrB | 5517 | p.Ile93Thr | missense_variant | 0.2 |
gyrB | 5724 | p.Ala162Val | missense_variant | 0.14 |
gyrB | 5772 | p.Ala178Asp | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8304 | p.Thr335Pro | missense_variant | 0.22 |
gyrA | 8994 | p.Asp565Tyr | missense_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9569 | p.Asp756Glu | missense_variant | 0.25 |
fgd1 | 490939 | p.Phe53Leu | missense_variant | 1.0 |
fgd1 | 491150 | p.Pro123Gln | missense_variant | 0.29 |
fgd1 | 491347 | p.Gly189Ser | missense_variant | 0.2 |
fgd1 | 491561 | p.His260Arg | missense_variant | 0.22 |
mshA | 575627 | p.Ala94Thr | missense_variant | 0.14 |
mshA | 576125 | p.Gly260* | stop_gained | 0.29 |
mshA | 576391 | c.1044G>T | synonymous_variant | 0.18 |
mshA | 576636 | p.Trp430Leu | missense_variant | 0.3 |
ccsA | 620176 | p.Val96Leu | missense_variant | 0.19 |
ccsA | 620185 | p.Gly99Cys | missense_variant | 0.14 |
ccsA | 620755 | p.Asp289Asn | missense_variant | 0.4 |
rpoB | 760013 | c.207C>T | synonymous_variant | 0.29 |
rpoB | 760239 | p.Thr145Ser | missense_variant | 0.25 |
rpoB | 760250 | p.Met148Ile | missense_variant | 0.18 |
rpoB | 760272 | p.Glu156* | stop_gained | 0.2 |
rpoB | 760545 | p.Gly247Trp | missense_variant | 1.0 |
rpoB | 761282 | c.1476C>A | synonymous_variant | 0.5 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.2 |
rpoB | 762174 | p.Val790Phe | missense_variant | 0.2 |
rpoC | 763771 | p.Tyr134* | stop_gained | 0.22 |
rpoC | 764253 | p.Arg295Leu | missense_variant | 0.4 |
rpoC | 764335 | c.966G>T | synonymous_variant | 0.33 |
rpoC | 764645 | p.Gly426Cys | missense_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765301 | c.1932C>T | synonymous_variant | 0.5 |
rpoC | 766832 | p.Glu1155* | stop_gained | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775769 | c.2712C>A | synonymous_variant | 0.25 |
mmpL5 | 776296 | p.Gln729Glu | missense_variant | 0.33 |
mmpL5 | 777082 | p.Lys467Gln | missense_variant | 0.4 |
mmpL5 | 777597 | p.Arg295Leu | missense_variant | 0.67 |
mmpL5 | 777876 | p.Arg202His | missense_variant | 0.17 |
mmpL5 | 778927 | c.-447C>A | upstream_gene_variant | 0.22 |
mmpR5 | 779335 | p.Asp116Tyr | missense_variant | 0.4 |
rplC | 801029 | p.Gly74Asp | missense_variant | 0.5 |
rplC | 801080 | p.Ala91Asp | missense_variant | 0.4 |
rplC | 801394 | p.Gly196Cys | missense_variant | 0.29 |
fbiC | 1303149 | c.219C>A | synonymous_variant | 0.17 |
fbiC | 1304161 | c.1235delG | frameshift_variant | 0.22 |
fbiC | 1304467 | p.Glu513Lys | missense_variant | 0.4 |
fbiC | 1305294 | p.Trp788Cys | missense_variant | 0.22 |
Rv1258c | 1407245 | p.Trp32Cys | missense_variant | 0.2 |
embR | 1416771 | p.Glu193* | stop_gained | 0.4 |
embR | 1417510 | c.-163C>A | upstream_gene_variant | 0.29 |
atpE | 1460972 | c.-73G>T | upstream_gene_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473540 | n.-118C>A | upstream_gene_variant | 0.5 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673707 | p.Gly90Ser | missense_variant | 0.67 |
inhA | 1674427 | p.Gly76Cys | missense_variant | 0.33 |
inhA | 1674556 | p.Gly119Cys | missense_variant | 0.25 |
inhA | 1674684 | p.Met161Ile | missense_variant | 0.25 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
rpsA | 1834958 | p.Leu473Met | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918670 | p.Arg244Leu | missense_variant | 0.25 |
ndh | 2101887 | p.Glu386* | stop_gained | 0.29 |
ndh | 2101930 | c.1113C>A | synonymous_variant | 0.5 |
ndh | 2102162 | p.Arg294Leu | missense_variant | 0.5 |
ndh | 2102884 | c.159G>T | synonymous_variant | 0.5 |
katG | 2155019 | p.Pro365Thr | missense_variant | 0.33 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
katG | 2156271 | c.-160G>T | upstream_gene_variant | 0.33 |
PPE35 | 2170103 | c.510C>A | synonymous_variant | 0.22 |
PPE35 | 2170737 | c.-125C>A | upstream_gene_variant | 0.33 |
PPE35 | 2170780 | c.-168G>T | upstream_gene_variant | 0.4 |
Rv1979c | 2221881 | c.1284G>T | synonymous_variant | 0.5 |
Rv1979c | 2222797 | p.Pro123His | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288690 | p.Cys184* | stop_gained | 0.18 |
pncA | 2290033 | c.-792C>A | upstream_gene_variant | 0.4 |
kasA | 2518207 | p.Ser31Arg | missense_variant | 0.33 |
kasA | 2518896 | p.Pro261Gln | missense_variant | 0.2 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2714307 | c.1026G>T | synonymous_variant | 0.5 |
eis | 2714569 | p.Ala255Asp | missense_variant | 0.5 |
eis | 2714745 | c.588C>A | synonymous_variant | 0.13 |
ahpC | 2726776 | p.Ala195Asp | missense_variant | 0.2 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
folC | 2746684 | c.915C>A | synonymous_variant | 0.29 |
folC | 2747072 | p.Gly176Phe | missense_variant | 0.67 |
folC | 2747284 | c.315G>T | synonymous_variant | 0.22 |
folC | 2747537 | p.Pro21Gln | missense_variant | 0.4 |
pepQ | 2860022 | p.Glu133* | stop_gained | 0.18 |
ribD | 2986835 | c.-4G>T | upstream_gene_variant | 0.25 |
ribD | 2987264 | c.426G>T | synonymous_variant | 0.22 |
Rv2752c | 3066027 | c.165C>A | synonymous_variant | 0.22 |
Rv2752c | 3066356 | c.-165G>T | upstream_gene_variant | 0.13 |
thyX | 3067377 | p.Arg190Pro | missense_variant | 0.22 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
fbiD | 3339124 | p.Gly3Cys | missense_variant | 0.33 |
fbiD | 3339214 | p.Gln33* | stop_gained | 0.18 |
fbiD | 3339235 | p.Leu40Met | missense_variant | 0.2 |
Rv3083 | 3449299 | p.Arg266Trp | missense_variant | 0.29 |
Rv3083 | 3449537 | p.Ala345Glu | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474096 | p.Glu30Asp | missense_variant | 0.29 |
fprA | 3475222 | p.Val406Leu | missense_variant | 0.22 |
fprA | 3475313 | p.Pro436Gln | missense_variant | 0.14 |
Rv3236c | 3612403 | c.714G>T | synonymous_variant | 0.29 |
Rv3236c | 3613084 | c.33C>A | synonymous_variant | 0.5 |
fbiB | 3640716 | c.-819C>A | upstream_gene_variant | 0.33 |
fbiB | 3641397 | c.-138G>T | upstream_gene_variant | 0.5 |
alr | 3840896 | p.Met175Ile | missense_variant | 0.25 |
ddn | 3986649 | c.-195G>T | upstream_gene_variant | 0.29 |
ddn | 3986802 | c.-42G>A | upstream_gene_variant | 0.5 |
ddn | 3986882 | c.39C>A | synonymous_variant | 0.67 |
ddn | 3986990 | c.147G>A | synonymous_variant | 0.33 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038875 | c.1830C>A | synonymous_variant | 0.17 |
panD | 4044425 | c.-144C>A | upstream_gene_variant | 0.22 |
embC | 4240033 | c.171G>T | synonymous_variant | 0.29 |
embC | 4240133 | p.Ala91Thr | missense_variant | 0.29 |
embC | 4240577 | p.Ala239Ser | missense_variant | 0.14 |
embC | 4240807 | c.945C>A | synonymous_variant | 0.18 |
embC | 4240836 | p.Gly325Val | missense_variant | 0.22 |
embC | 4240850 | p.Leu330Met | missense_variant | 0.18 |
embC | 4241074 | c.1212G>T | synonymous_variant | 0.18 |
embC | 4241581 | c.1719C>A | synonymous_variant | 0.4 |
embC | 4241611 | c.1749G>T | synonymous_variant | 0.67 |
embC | 4242426 | p.Arg855Gln | missense_variant | 0.22 |
embC | 4242619 | p.Asp919Glu | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244086 | p.Pro285Gln | missense_variant | 0.2 |
embA | 4244279 | c.1047G>A | synonymous_variant | 0.18 |
embB | 4246796 | p.Gly95Cys | missense_variant | 0.22 |
embB | 4247009 | p.Asp166Tyr | missense_variant | 0.18 |
embB | 4247059 | c.546C>T | synonymous_variant | 0.14 |
embB | 4247560 | p.Trp349Cys | missense_variant | 0.2 |
embB | 4248317 | p.Val602Leu | missense_variant | 0.22 |
embB | 4248466 | p.Ser651Arg | missense_variant | 0.22 |
aftB | 4268655 | p.Thr61Ile | missense_variant | 0.22 |
ubiA | 4269855 | c.-22G>T | upstream_gene_variant | 0.22 |
ubiA | 4269935 | c.-102C>A | upstream_gene_variant | 0.18 |
ethR | 4326940 | c.-609G>T | upstream_gene_variant | 0.33 |
ethA | 4328412 | c.-939G>T | upstream_gene_variant | 0.15 |
ethA | 4328470 | c.-997G>C | upstream_gene_variant | 0.15 |
whiB6 | 4338277 | p.Pro82His | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |