Run ID: ERR2679270
Sample name:
Date: 31-03-2023 23:00:45
Number of reads: 310936
Percentage reads mapped: 94.31
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.12 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.12 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.13 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.13 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.13 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.13 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.13 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.12 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.12 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.12 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.14 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.15 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.14 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.12 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.33 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.29 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776383 | c.2097delC | frameshift_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406195 | c.1146G>A | synonymous_variant | 0.11 |
embR | 1416432 | p.Ala306Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475907 | n.2253delA | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833924 | p.Gly128Asp | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168981 | c.1632A>G | synonymous_variant | 0.17 |
PPE35 | 2169253 | p.Ala454Thr | missense_variant | 0.15 |
PPE35 | 2169783 | p.Thr277Lys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290179 | c.-938G>T | upstream_gene_variant | 0.2 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ribD | 2987231 | c.393G>T | synonymous_variant | 0.14 |
Rv2752c | 3065553 | c.639A>G | synonymous_variant | 0.15 |
Rv2752c | 3065562 | c.630T>C | synonymous_variant | 0.15 |
Rv2752c | 3065569 | p.Ile208His | missense_variant | 0.15 |
Rv2752c | 3065576 | p.Ala206Ser | missense_variant | 0.15 |
Rv2752c | 3065577 | c.615C>T | synonymous_variant | 0.15 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.15 |
Rv2752c | 3065583 | c.609G>A | synonymous_variant | 0.14 |
Rv2752c | 3065594 | c.598C>T | synonymous_variant | 0.12 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.12 |
Rv2752c | 3065607 | c.585C>G | synonymous_variant | 0.12 |
Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 0.12 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.17 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.17 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.17 |
Rv2752c | 3066054 | c.138T>C | synonymous_variant | 0.17 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.13 |
Rv2752c | 3066071 | c.121T>C | synonymous_variant | 0.13 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.13 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449135 | p.Gln211Arg | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.14 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.14 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.16 |
rpoA | 3878276 | c.232C>T | synonymous_variant | 0.15 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |