Run ID: ERR2653062
Sample name:
Date: 31-03-2023 22:28:32
Number of reads: 1029515
Percentage reads mapped: 99.42
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 | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5853 | p.Thr205Ile | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.96 |
gyrA | 9083 | c.1782G>A | synonymous_variant | 0.11 |
gyrA | 9084 | p.His595Asp | missense_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 763310 | c.3506_3507delAG | frameshift_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776581 | c.1900C>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406416 | p.Pro309Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475199 | n.1542G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475575 | n.1918C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475662 | n.2005C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476113 | n.2456T>A | non_coding_transcript_exon_variant | 0.15 |
tlyA | 1917822 | c.-118G>C | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154102 | c.2010C>G | synonymous_variant | 0.11 |
katG | 2155732 | p.Gln127Arg | missense_variant | 0.1 |
PPE35 | 2168895 | p.Gly573Phe | missense_variant | 0.25 |
Rv1979c | 2222769 | p.Gln132His | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086927 | c.108G>A | synonymous_variant | 0.13 |
ald | 3086957 | c.138C>T | synonymous_variant | 0.25 |
ald | 3087405 | p.Val196Ile | missense_variant | 1.0 |
ald | 3087531 | p.Ala238Ser | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612201 | p.Val306Leu | missense_variant | 0.1 |
fbiB | 3642694 | p.Ala387Val | missense_variant | 0.13 |
alr | 3840962 | c.459G>A | synonymous_variant | 0.12 |
rpoA | 3878122 | p.Asn129Ser | missense_variant | 0.11 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.16 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | p.Gln579His | missense_variant | 0.11 |
embC | 4239741 | c.-122C>A | upstream_gene_variant | 0.12 |
embC | 4241341 | p.Phe493Leu | missense_variant | 0.14 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245656 | c.-858C>T | upstream_gene_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.11 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.12 |
aftB | 4268605 | p.Arg78Ser | missense_variant | 0.12 |
aftB | 4268870 | c.-34G>T | upstream_gene_variant | 0.12 |
ethA | 4326024 | p.Pro484Thr | missense_variant | 0.94 |
ethR | 4327574 | p.Ala9Asp | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |