Run ID: SRR12830378
Sample name:
Date: 03-04-2023 06:58:42
Number of reads: 446086
Percentage reads mapped: 99.77
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8194 | p.Gly298Asp | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9382 | p.Gly694Val | missense_variant | 0.12 |
rpoB | 762006 | p.Arg734Gly | missense_variant | 0.12 |
rpoC | 763247 | c.-123G>A | upstream_gene_variant | 0.13 |
rpoC | 763824 | p.Glu152Gly | missense_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779298 | c.-818G>T | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303350 | p.Cys140* | stop_gained | 0.15 |
embR | 1417524 | c.-177G>T | upstream_gene_variant | 0.22 |
atpE | 1460944 | c.-101T>A | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472180 | n.335A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473514 | n.-144C>T | upstream_gene_variant | 0.29 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475239 | n.1582A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.12 |
inhA | 1673408 | c.-794G>T | upstream_gene_variant | 0.11 |
inhA | 1673832 | c.-370A>G | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102308 | c.735G>A | synonymous_variant | 1.0 |
ndh | 2103197 | c.-155T>C | upstream_gene_variant | 0.15 |
katG | 2154008 | p.Ser702Thr | missense_variant | 0.12 |
katG | 2154233 | p.Leu627Met | missense_variant | 0.12 |
katG | 2155578 | p.Phe178Leu | missense_variant | 0.13 |
PPE35 | 2169497 | c.1116C>T | synonymous_variant | 0.18 |
PPE35 | 2169608 | c.1005C>T | synonymous_variant | 0.25 |
Rv1979c | 2221884 | c.1281G>T | synonymous_variant | 0.14 |
Rv1979c | 2222960 | p.Ala69Ser | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
pepQ | 2859671 | p.Tyr250His | missense_variant | 0.11 |
Rv2752c | 3066064 | p.Ile43Asn | missense_variant | 0.13 |
thyX | 3067717 | p.Ser77Gly | missense_variant | 0.1 |
thyX | 3067887 | p.Pro20Gln | missense_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449854 | p.Met451Val | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641930 | p.Leu132Phe | missense_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249606 | c.3093C>T | synonymous_variant | 0.15 |
ethA | 4326569 | p.Phe302Ser | missense_variant | 0.11 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |