Run ID: ERR8774177
Sample name:
Date: 02-04-2023 08:24:49
Number of reads: 207454
Percentage reads mapped: 99.54
Strain: lineage4.3.4.2.1
Drug-resistance: RR-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 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761095 | p.Leu430Pro | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5323 | c.84A>G | synonymous_variant | 0.29 |
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620529 | c.639G>T | synonymous_variant | 0.29 |
rpoB | 761657 | c.1851C>A | synonymous_variant | 0.4 |
rpoB | 762313 | p.Gly836Val | missense_variant | 0.25 |
rpoC | 762959 | c.-411G>T | upstream_gene_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775800 | p.Ser894* | stop_gained | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673603 | p.Leu55Pro | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918068 | c.129C>T | synonymous_variant | 0.22 |
katG | 2155383 | c.729C>A | synonymous_variant | 0.33 |
PPE35 | 2169980 | c.633C>T | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746929 | p.Pro224Thr | missense_variant | 0.29 |
folC | 2747537 | p.Pro21Leu | missense_variant | 0.29 |
pepQ | 2859373 | p.Pro349Leu | missense_variant | 0.25 |
thyX | 3067335 | p.Ala204Asp | missense_variant | 0.3 |
thyX | 3067418 | c.528C>A | synonymous_variant | 0.2 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087893 | p.Asp358Glu | missense_variant | 0.18 |
Rv3083 | 3449160 | c.657G>A | synonymous_variant | 0.2 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3612793 | c.324C>A | synonymous_variant | 0.29 |
fbiB | 3641642 | c.108G>T | synonymous_variant | 0.33 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039152 | p.Ile518Thr | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244524 | p.Pro431Gln | missense_variant | 0.15 |
embA | 4245465 | p.Pro745Thr | missense_variant | 0.22 |
aftB | 4267742 | c.1095G>T | synonymous_variant | 0.4 |
aftB | 4269345 | c.-509C>A | upstream_gene_variant | 0.5 |
ethA | 4328398 | c.-925C>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |