Run ID: ERR1215483
Sample name:
Date: 31-03-2023 12:47:11
Number of reads: 528020
Percentage reads mapped: 97.52
Strain: lineage4.3.1
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 |
lineage4.3.1 | Euro-American (LAM) | LAM9 | None | 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 | 8930 | c.1629C>T | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.93 |
rpoB | 759776 | c.-31T>G | upstream_gene_variant | 0.22 |
rpoB | 760493 | c.687C>T | synonymous_variant | 0.17 |
rpoB | 760519 | p.Thr238Ile | missense_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765219 | p.Glu617Gly | missense_variant | 0.13 |
rpoC | 765781 | c.2412C>T | synonymous_variant | 0.14 |
rpoC | 766901 | p.Gly1178Ser | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800830 | p.Gly8Ser | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476007 | n.2350T>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156404 | c.-293G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289412 | c.-171C>T | upstream_gene_variant | 0.14 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449945 | p.Gly481Asp | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040167 | p.Ala180Thr | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245308 | c.2076G>A | synonymous_variant | 0.15 |
embB | 4246643 | p.Thr44Ala | missense_variant | 0.18 |
embB | 4249404 | p.Thr964Ile | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |