Run ID: ERR2229391
Sample name:
Date: 31-03-2023 17:08:59
Number of reads: 571576
Percentage reads mapped: 98.82
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918342 | c.404_405delAC | frameshift_variant | 0.29 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5959 | c.720C>G | synonymous_variant | 0.25 |
gyrB | 6701 | p.Val488Leu | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8092 | p.Arg264Leu | missense_variant | 0.12 |
fgd1 | 490853 | p.Ala24Asp | missense_variant | 0.12 |
rpoB | 759977 | p.Trp57* | stop_gained | 0.2 |
rpoB | 761157 | p.Ala451Ser | missense_variant | 0.25 |
rpoB | 763106 | p.Ile1100Met | missense_variant | 0.2 |
rpoC | 763775 | p.Ile136Phe | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775881 | p.Asn867Ser | missense_variant | 0.33 |
mmpL5 | 776222 | c.2258delG | frameshift_variant | 0.5 |
mmpL5 | 777061 | p.Ala474Pro | missense_variant | 0.18 |
mmpL5 | 778926 | c.-446A>G | upstream_gene_variant | 0.17 |
mmpR5 | 779121 | c.138_139dupTG | frameshift_variant | 0.33 |
mmpS5 | 779661 | c.-756C>A | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474644 | n.987G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474925 | n.1268G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475506 | n.1849A>G | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.42 |
rpsA | 1834047 | p.Ile169Thr | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918150 | p.Val71Phe | missense_variant | 0.17 |
ndh | 2102751 | p.Cys98Ser | missense_variant | 0.22 |
katG | 2154193 | p.Arg640His | missense_variant | 0.33 |
katG | 2155083 | c.1029G>A | synonymous_variant | 0.14 |
katG | 2155355 | c.757C>A | synonymous_variant | 0.18 |
katG | 2155813 | p.Pro100Leu | missense_variant | 0.4 |
katG | 2156387 | c.-276T>A | upstream_gene_variant | 0.2 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.2 |
PPE35 | 2168622 | p.Ala664Asp | missense_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.16 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.21 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.21 |
PPE35 | 2169351 | p.Ala421His | missense_variant | 0.17 |
PPE35 | 2169587 | c.1026G>C | synonymous_variant | 0.14 |
PPE35 | 2169605 | c.1008T>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.81 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.85 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289401 | c.-160G>T | upstream_gene_variant | 0.18 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.4 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.4 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.33 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.33 |
eis | 2714156 | p.Asp393Tyr | missense_variant | 0.2 |
ahpC | 2725935 | c.-258G>T | upstream_gene_variant | 0.17 |
ahpC | 2726431 | p.Ala80Gly | missense_variant | 0.22 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.18 |
thyX | 3067774 | p.Ala58Ser | missense_variant | 0.29 |
thyA | 3074056 | p.Glu139Gly | missense_variant | 0.33 |
ald | 3086839 | p.Thr7Ile | missense_variant | 0.17 |
fbiB | 3640554 | c.-981C>A | upstream_gene_variant | 0.25 |
fbiA | 3640817 | p.Leu92Arg | missense_variant | 0.25 |
fbiA | 3640888 | c.349delC | frameshift_variant | 0.5 |
fbiA | 3641363 | p.Arg274Pro | missense_variant | 0.15 |
fbiB | 3642594 | p.Pro354Ser | missense_variant | 0.25 |
alr | 3841012 | p.Gln137Lys | missense_variant | 0.33 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
rpoA | 3878069 | p.Val147Phe | missense_variant | 0.33 |
clpC1 | 4039042 | p.Ser555Thr | missense_variant | 0.2 |
clpC1 | 4039193 | c.1512C>G | synonymous_variant | 0.29 |
clpC1 | 4039205 | c.1500C>A | synonymous_variant | 0.25 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.4 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.8 |
panD | 4044071 | p.Ile71Phe | missense_variant | 0.22 |
panD | 4044314 | c.-33C>A | upstream_gene_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242910 | p.Phe1016Leu | missense_variant | 0.29 |
embC | 4243092 | p.Leu1077Arg | missense_variant | 0.12 |
embA | 4243096 | c.-137A>C | upstream_gene_variant | 0.12 |
embA | 4243099 | c.-134G>C | upstream_gene_variant | 0.12 |
embA | 4243102 | c.-131G>T | upstream_gene_variant | 0.12 |
embC | 4243103 | p.Thr1081Pro | missense_variant | 0.12 |
embC | 4243106 | p.Arg1082Ser | missense_variant | 0.12 |
embA | 4243371 | p.Gln47Lys | missense_variant | 0.33 |
embA | 4245235 | p.Met668Lys | missense_variant | 0.33 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.83 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.67 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.83 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.67 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.5 |
embB | 4247426 | p.Gly305Thr | missense_variant | 0.2 |
embB | 4248030 | p.Thr506Asn | missense_variant | 0.18 |
aftB | 4266982 | p.Asp619Tyr | missense_variant | 0.33 |
aftB | 4267761 | p.Asp359Gly | missense_variant | 0.43 |
ubiA | 4269269 | p.Ala189Ser | missense_variant | 0.17 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.18 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.18 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.18 |
ethA | 4328323 | c.-850T>C | upstream_gene_variant | 0.12 |
whiB6 | 4338485 | p.Asn13Asp | missense_variant | 0.22 |
whiB6 | 4338574 | c.-53G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |