Run ID: SRR4035807
Sample name:
Date: 18-08-2022 14:03:18
Number of reads: 817043
Percentage reads mapped: 99.52
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5715 | p.Lys159Met | missense_variant | 0.17 |
gyrB | 6145 | c.906C>T | synonymous_variant | 0.14 |
gyrB | 6180 | p.Gly314Asp | missense_variant | 0.14 |
gyrA | 8372 | c.1071G>A | synonymous_variant | 0.14 |
gyrA | 8727 | p.Arg476Cys | missense_variant | 0.18 |
gyrA | 9306 | p.Asp669His | missense_variant | 0.18 |
gyrA | 9370 | p.Leu690Pro | missense_variant | 0.2 |
fgd1 | 490747 | c.-36C>T | upstream_gene_variant | 0.15 |
fgd1 | 491280 | c.498C>T | synonymous_variant | 0.18 |
fgd1 | 491299 | p.Tyr173Asn | missense_variant | 0.18 |
fgd1 | 491418 | c.636A>G | synonymous_variant | 0.14 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575300 | c.-48A>T | upstream_gene_variant | 0.14 |
mshA | 576069 | p.Gly241Val | missense_variant | 0.16 |
mshA | 576317 | p.Arg324Trp | missense_variant | 0.2 |
rpoB | 759908 | c.102C>T | synonymous_variant | 0.18 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.92 |
rpoB | 761061 | p.Ala419Thr | missense_variant | 0.14 |
rpoB | 761099 | c.1293C>T | synonymous_variant | 0.14 |
rpoB | 761288 | c.1482G>A | synonymous_variant | 0.13 |
rpoC | 763700 | p.Pro111Ser | missense_variant | 0.12 |
rpoC | 763709 | c.341dupT | frameshift_variant | 0.13 |
rpoC | 763838 | p.Val157Met | missense_variant | 0.12 |
rpoC | 764263 | c.894G>A | synonymous_variant | 0.94 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.13 |
rpoC | 764590 | p.Lys407Asn | missense_variant | 0.15 |
rpsL | 781365 | c.-195T>A | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781402 | c.-158A>T | upstream_gene_variant | 0.14 |
rpsL | 781834 | p.Gly92Ala | missense_variant | 0.14 |
rplC | 800926 | p.Arg40Gly | missense_variant | 0.11 |
rplC | 801075 | c.267G>T | synonymous_variant | 0.13 |
fbiC | 1303121 | p.Arg64Gln | missense_variant | 0.15 |
fbiC | 1303132 | p.Ala68Thr | missense_variant | 0.15 |
fbiC | 1303735 | p.Glu269Lys | missense_variant | 0.15 |
fbiC | 1303740 | c.810C>T | synonymous_variant | 0.18 |
fbiC | 1304142 | c.1212G>A | synonymous_variant | 0.18 |
fbiC | 1305142 | p.Glu738* | stop_gained | 0.15 |
fbiC | 1305248 | p.Ala773Val | missense_variant | 0.14 |
atpE | 1460940 | c.-105C>A | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673400 | c.-40C>T | upstream_gene_variant | 0.17 |
inhA | 1673715 | c.-487C>G | upstream_gene_variant | 0.15 |
inhA | 1674675 | c.474C>T | synonymous_variant | 0.17 |
inhA | 1674686 | p.Thr162Met | missense_variant | 0.17 |
rpsA | 1833475 | c.-67G>A | upstream_gene_variant | 0.14 |
rpsA | 1833854 | p.Lys105Glu | missense_variant | 0.15 |
rpsA | 1834715 | p.Phe392Ile | missense_variant | 0.15 |
tlyA | 1917945 | c.6A>G | synonymous_variant | 0.18 |
tlyA | 1917953 | p.Ala5Val | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155576 | p.Lys179Arg | missense_variant | 0.12 |
pncA | 2289884 | c.-643G>A | upstream_gene_variant | 0.18 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518135 | c.21T>C | synonymous_variant | 0.1 |
kasA | 2519049 | p.Gly312Asp | missense_variant | 0.17 |
eis | 2714761 | p.Leu191Pro | missense_variant | 0.18 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.12 |
ahpC | 2726083 | c.-110G>A | upstream_gene_variant | 0.2 |
ahpC | 2726732 | p.Lys180Asn | missense_variant | 0.14 |
folC | 2747241 | p.Tyr120Asn | missense_variant | 0.13 |
folC | 2747608 | c.-10C>A | upstream_gene_variant | 0.17 |
pepQ | 2860444 | c.-26C>T | upstream_gene_variant | 0.14 |
thyX | 3067796 | c.150C>T | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087291 | p.Val158Met | missense_variant | 0.17 |
fbiA | 3641331 | c.793delG | frameshift_variant | 0.2 |
fbiB | 3641407 | c.-128C>T | upstream_gene_variant | 0.13 |
fbiA | 3641428 | p.Ala296Thr | missense_variant | 0.15 |
fbiB | 3642202 | p.Ser223Phe | missense_variant | 0.2 |
fbiB | 3642648 | p.Met372Val | missense_variant | 0.18 |
panD | 4044010 | p.Ala91Glu | missense_variant | 0.17 |
panD | 4044258 | c.24G>C | synonymous_variant | 0.17 |
embC | 4240966 | c.1104G>A | synonymous_variant | 0.14 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244197 | p.Val322Ala | missense_variant | 0.15 |
embA | 4244626 | p.Leu465Pro | missense_variant | 0.17 |
embB | 4245869 | c.-645C>A | upstream_gene_variant | 0.14 |
embB | 4247646 | p.Glu378Gly | missense_variant | 0.12 |
embB | 4247653 | c.1140C>T | synonymous_variant | 0.13 |
embB | 4247765 | c.1252C>T | synonymous_variant | 0.14 |
embB | 4249427 | p.Arg972Cys | missense_variant | 0.17 |
embB | 4249735 | c.3222T>A | synonymous_variant | 0.13 |
ubiA | 4269656 | p.Val60Leu | missense_variant | 0.15 |
ubiA | 4269671 | p.Val55Leu | missense_variant | 0.13 |
ubiA | 4269905 | c.-72G>A | upstream_gene_variant | 0.13 |
ethA | 4326063 | p.Gly471Ser | missense_variant | 0.15 |
ethA | 4326177 | p.Glu433Gln | missense_variant | 0.18 |
gid | 4407849 | c.354C>T | synonymous_variant | 0.17 |
gid | 4408311 | c.-109C>T | upstream_gene_variant | 0.18 |