Run ID: SRR3743189
Sample name:
Date: 04-04-2023 05:40:28
Number of reads: 1811621
Percentage reads mapped: 99.01
Strain: lineage4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.18 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 0.11 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7156 | p.Asp639Glu | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8461 | c.1161delA | frameshift_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491123 | p.Ile114Thr | missense_variant | 0.12 |
mshA | 575865 | p.Leu173Ser | missense_variant | 0.18 |
mshA | 576766 | c.1419G>T | synonymous_variant | 0.12 |
rpoB | 759930 | p.Leu42Ile | missense_variant | 0.1 |
rpoC | 763616 | c.250delC | frameshift_variant | 0.12 |
rpoC | 763735 | c.366G>T | synonymous_variant | 1.0 |
rpoC | 764220 | p.Gly284Val | missense_variant | 0.12 |
rpoC | 764725 | p.Phe452Leu | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775968 | p.Met838Thr | missense_variant | 0.12 |
mmpL5 | 778960 | c.-480G>T | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781414 | c.-146G>A | upstream_gene_variant | 0.11 |
fbiC | 1303537 | c.607C>A | synonymous_variant | 0.29 |
embR | 1416359 | p.Ala330Asp | missense_variant | 0.13 |
embR | 1416788 | p.Ala187Asp | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673560 | p.Lys41His | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918606 | p.Val223Ile | missense_variant | 0.11 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.18 |
katG | 2155255 | p.Pro286Arg | missense_variant | 0.13 |
katG | 2155371 | c.741C>T | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2170331 | c.282G>T | synonymous_variant | 0.13 |
Rv1979c | 2222804 | p.Ala121Thr | missense_variant | 0.15 |
Rv1979c | 2222834 | p.Ser111Pro | missense_variant | 0.15 |
Rv1979c | 2222926 | p.Ala80Asp | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288714 | c.528C>A | synonymous_variant | 0.12 |
pncA | 2290159 | c.-918A>C | upstream_gene_variant | 0.25 |
pncA | 2290202 | c.-961C>T | upstream_gene_variant | 0.12 |
thyX | 3067387 | p.Gly187Cys | missense_variant | 0.18 |
thyX | 3067699 | c.246delC | frameshift_variant | 0.12 |
thyX | 3067923 | p.Arg8Leu | missense_variant | 0.13 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087397 | p.Thr193Ile | missense_variant | 0.11 |
Rv3083 | 3448752 | c.250delT | frameshift_variant | 0.11 |
Rv3083 | 3449617 | c.1116delC | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474817 | p.Phe271Leu | missense_variant | 0.25 |
Rv3236c | 3612024 | p.Val365Phe | missense_variant | 0.13 |
Rv3236c | 3612931 | c.186G>T | synonymous_variant | 0.11 |
fbiB | 3641736 | p.Glu68Lys | missense_variant | 0.17 |
rpoA | 3878347 | p.Ile54Thr | missense_variant | 0.11 |
clpC1 | 4039421 | c.1283delT | frameshift_variant | 0.15 |
embC | 4240049 | c.191delA | frameshift_variant | 0.13 |
embC | 4242444 | p.Pro861Leu | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244942 | p.Trp570Cys | missense_variant | 0.25 |
embA | 4245645 | p.Ala805Pro | missense_variant | 0.13 |
embA | 4246030 | p.Pro933Gln | missense_variant | 0.11 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.2 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
aftB | 4267604 | c.1233C>A | synonymous_variant | 0.12 |
aftB | 4267905 | c.928_931dupGCCG | frameshift_variant | 0.29 |
ethR | 4326778 | c.-771G>A | upstream_gene_variant | 1.0 |
ethR | 4326949 | c.-600A>G | upstream_gene_variant | 0.12 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.97 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |