Run ID: ERR9285885
Sample name:
Date: 02-04-2023 11:43:39
Number of reads: 791909
Percentage reads mapped: 99.67
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 0.99 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491190 | c.408G>A | synonymous_variant | 0.14 |
mshA | 575543 | p.Gly66Ser | missense_variant | 0.11 |
mshA | 576089 | c.750_769delTGATCGGCGCGCGGCCCGGG | frameshift_variant | 0.15 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304346 | p.Asp472Glu | missense_variant | 0.1 |
Rv1258c | 1407429 | c.-89G>T | upstream_gene_variant | 0.1 |
embR | 1416232 | c.1116T>C | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473085 | n.1240A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918712 | p.Asp258Gly | missense_variant | 0.11 |
ndh | 2101831 | c.1212G>T | synonymous_variant | 0.12 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.11 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.1 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.11 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.11 |
PPE35 | 2168421 | p.Val731Asp | missense_variant | 0.11 |
PPE35 | 2169071 | c.1542A>T | synonymous_variant | 0.29 |
PPE35 | 2169125 | p.Val496Ile | missense_variant | 0.25 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.19 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.17 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.17 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.16 |
PPE35 | 2169623 | c.990T>C | synonymous_variant | 0.17 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.23 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.17 |
Rv1979c | 2221754 | p.Ile471Val | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714838 | p.Leu165Phe | missense_variant | 0.17 |
folC | 2746510 | c.1089A>T | synonymous_variant | 0.11 |
folC | 2746923 | p.Gly226Ser | missense_variant | 1.0 |
folC | 2747545 | c.54G>A | synonymous_variant | 0.12 |
ribD | 2987355 | p.Val173Phe | missense_variant | 0.11 |
thyA | 3073719 | c.753C>T | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3449869 | p.Ser456Pro | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612088 | c.1029G>A | synonymous_variant | 0.11 |
Rv3236c | 3612547 | c.570C>T | synonymous_variant | 0.14 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
fbiB | 3641994 | p.Arg154Ser | missense_variant | 0.12 |
rpoA | 3878496 | c.12A>G | synonymous_variant | 0.11 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.17 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.17 |
clpC1 | 4040838 | c.-134C>T | upstream_gene_variant | 0.11 |
embC | 4241577 | p.Thr572Met | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243692 | p.Gly154Ser | missense_variant | 1.0 |
embA | 4244117 | c.885G>C | synonymous_variant | 0.1 |
embA | 4244119 | p.Tyr296Trp | missense_variant | 0.1 |
embB | 4246904 | p.Val131Met | missense_variant | 1.0 |
ethA | 4328252 | c.-779T>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |