Run ID: ERR2229138
Sample name:
Date: 31-03-2023 16:43:47
Number of reads: 620472
Percentage reads mapped: 99.42
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4327054 | p.Tyr140* | stop_gained | 0.12 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6094 | c.855C>T | synonymous_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 490649 | c.-134C>T | upstream_gene_variant | 0.13 |
fgd1 | 491012 | p.Pro77His | missense_variant | 0.25 |
rpoB | 760918 | p.Arg371His | missense_variant | 0.12 |
rpoB | 761961 | p.Pro719Ser | missense_variant | 0.15 |
rpoC | 762503 | c.-867G>A | upstream_gene_variant | 0.11 |
rpoC | 763860 | p.Asp164Val | missense_variant | 0.15 |
rpoC | 764214 | p.Arg282Gln | missense_variant | 0.15 |
rpoC | 766958 | p.Gly1197Cys | missense_variant | 0.25 |
mmpL5 | 775596 | p.Ala962Asp | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801320 | p.Gly171Val | missense_variant | 0.13 |
fbiC | 1302738 | c.-193G>A | upstream_gene_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406179 | p.Val388Leu | missense_variant | 0.12 |
Rv1258c | 1406306 | c.1035C>A | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.18 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.18 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.18 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.28 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918516 | p.Gly193Ser | missense_variant | 0.15 |
ndh | 2101877 | p.Gly389Asp | missense_variant | 0.18 |
ndh | 2102647 | c.396C>T | synonymous_variant | 0.14 |
katG | 2155143 | p.Asn323Lys | missense_variant | 0.25 |
katG | 2156263 | c.-152A>G | upstream_gene_variant | 0.2 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.53 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.55 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289939 | c.-698G>T | upstream_gene_variant | 0.22 |
kasA | 2518348 | c.234A>T | synonymous_variant | 0.17 |
folC | 2747147 | p.Lys151Arg | missense_variant | 0.2 |
pepQ | 2860476 | c.-58A>G | upstream_gene_variant | 0.14 |
whiB7 | 3568608 | c.72T>C | synonymous_variant | 0.11 |
Rv3236c | 3612670 | c.447G>T | synonymous_variant | 0.22 |
fbiB | 3640617 | c.-918G>A | upstream_gene_variant | 0.15 |
fbiA | 3640870 | p.Ala110Ser | missense_variant | 0.14 |
alr | 3840436 | c.985C>T | synonymous_variant | 0.12 |
ddn | 3986715 | c.-129A>T | upstream_gene_variant | 0.14 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.2 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.13 |
embC | 4241968 | c.2106A>G | synonymous_variant | 0.22 |
embC | 4242166 | c.2304G>C | synonymous_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245488 | c.2256G>T | synonymous_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.67 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.75 |
embB | 4246555 | c.42G>C | synonymous_variant | 1.0 |
embB | 4246556 | p.Ala15Pro | missense_variant | 1.0 |
embB | 4246563 | p.Leu17Trp | missense_variant | 1.0 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247643 | p.Val377Glu | missense_variant | 0.17 |
embB | 4249311 | p.Arg933His | missense_variant | 0.12 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.15 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.15 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.14 |
ethA | 4327420 | p.Ser18Arg | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |