Run ID: ERR1633799
Sample name:
Date: 18-08-2022 14:46:56
Number of reads: 1202516
Percentage reads mapped: 99.58
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.99 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 5961 | p.Thr241Asn | missense_variant | 0.12 |
gyrB | 6549 | p.Gly437Val | missense_variant | 0.13 |
gyrA | 6565 | c.-737G>A | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8771 | c.1470C>T | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 760572 | c.766C>T | synonymous_variant | 0.13 |
rpoC | 763340 | c.-30T>C | upstream_gene_variant | 0.12 |
rpoC | 763363 | c.-7G>A | upstream_gene_variant | 0.15 |
rpoC | 764279 | p.Gln304Lys | missense_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766960 | c.3591C>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472334 | n.489A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834758 | p.Gly406Glu | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155270 | p.Ala281Gly | missense_variant | 0.18 |
katG | 2155941 | c.171G>T | synonymous_variant | 0.2 |
pncA | 2289955 | c.-714C>A | upstream_gene_variant | 0.15 |
kasA | 2518222 | c.108G>T | synonymous_variant | 1.0 |
folC | 2746166 | p.Ala478Val | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086666 | c.-154G>A | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
panD | 4044045 | c.237G>T | synonymous_variant | 0.13 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.21 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.23 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246598 | p.Val29Leu | missense_variant | 0.15 |
ethA | 4326135 | p.Pro447Ser | missense_variant | 0.14 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |