Run ID: SRR15399219
Sample name:
Date: 03-04-2023 14:10:49
Number of reads: 5772943
Percentage reads mapped: 99.73
Strain: lineage4.3.4.2
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.98 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.97 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 0.98 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5076 | c.-164_-163insT | upstream_gene_variant | 0.98 |
gyrB | 6140 | p.Val301Leu | missense_variant | 0.98 |
gyrA | 6580 | c.-722C>G | upstream_gene_variant | 0.95 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.97 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 0.97 |
fbiA | 3640390 | c.-153A>G | upstream_gene_variant | 0.98 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.98 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.98 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.19 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.99 |