Run ID: ERR2229737
Sample name:
Date: 31-03-2023 17:30:04
Number of reads: 566953
Percentage reads mapped: 99.2
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2155532 | c.579delC | frameshift_variant | 0.2 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8406 | p.Gln369* | stop_gained | 0.12 |
mshA | 575256 | c.-92C>T | upstream_gene_variant | 0.13 |
mshA | 575418 | p.Ala24Asp | missense_variant | 0.2 |
ccsA | 619880 | c.-11A>T | upstream_gene_variant | 0.2 |
rpoB | 760294 | p.Asn163Ile | missense_variant | 0.14 |
rpoB | 760979 | p.Glu391Asp | missense_variant | 0.22 |
rpoC | 764840 | p.Ile491Val | missense_variant | 0.11 |
rpoC | 765761 | p.Pro798Ala | missense_variant | 0.2 |
rpoC | 765922 | c.2553C>T | synonymous_variant | 0.38 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778405 | p.Arg26Gly | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304140 | p.Ala404Ser | missense_variant | 0.25 |
fbiC | 1304399 | p.Arg490His | missense_variant | 0.13 |
embR | 1417481 | c.-134G>T | upstream_gene_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472280 | n.435C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.27 |
fabG1 | 1673771 | p.Ala111Asp | missense_variant | 0.22 |
inhA | 1674253 | p.Asp18Asn | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918540 | p.Pro201Thr | missense_variant | 0.17 |
ndh | 2103174 | c.-132G>T | upstream_gene_variant | 0.17 |
katG | 2154117 | c.1995T>G | synonymous_variant | 0.12 |
katG | 2154620 | p.Arg498Ser | missense_variant | 0.14 |
katG | 2155506 | c.606C>T | synonymous_variant | 0.14 |
PPE35 | 2167742 | c.2871C>A | synonymous_variant | 0.5 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.18 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.18 |
PPE35 | 2168687 | c.1926C>A | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168888 | c.1725G>T | synonymous_variant | 0.22 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.19 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.18 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.12 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.13 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.13 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.12 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.15 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.15 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.53 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.53 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.25 |
PPE35 | 2170155 | p.Ala153Gly | missense_variant | 0.3 |
PPE35 | 2170157 | c.456G>C | synonymous_variant | 0.3 |
PPE35 | 2170319 | p.Glu98Asp | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289258 | c.-17G>T | upstream_gene_variant | 0.12 |
eis | 2715267 | c.66C>A | synonymous_variant | 0.12 |
eis | 2715427 | c.-95T>C | upstream_gene_variant | 0.25 |
folC | 2746374 | p.Pro409Ala | missense_variant | 0.22 |
pepQ | 2860359 | c.60T>C | synonymous_variant | 0.14 |
Rv2752c | 3064901 | p.Leu431Val | missense_variant | 0.29 |
Rv2752c | 3064906 | p.Val429Ala | missense_variant | 0.25 |
Rv2752c | 3066126 | c.66C>A | synonymous_variant | 0.12 |
thyX | 3067953 | c.-8T>C | upstream_gene_variant | 0.12 |
thyA | 3074659 | c.-188G>A | upstream_gene_variant | 0.13 |
fprA | 3474199 | p.Lys65Glu | missense_variant | 0.17 |
fprA | 3474840 | c.834C>A | synonymous_variant | 0.22 |
fbiA | 3640813 | p.Glu91Gln | missense_variant | 0.1 |
alr | 3840844 | c.576delG | frameshift_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
rpoA | 3877730 | p.Ser260Ala | missense_variant | 0.14 |
clpC1 | 4038829 | p.Glu626Gln | missense_variant | 0.12 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.15 |
panD | 4044371 | c.-90G>T | upstream_gene_variant | 0.13 |
embC | 4240466 | p.Thr202Ala | missense_variant | 0.12 |
embC | 4240769 | p.Val303Met | missense_variant | 0.12 |
embC | 4242063 | p.Trp734Leu | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244371 | p.Arg380His | missense_variant | 0.2 |
embB | 4249140 | p.Val876Glu | missense_variant | 0.19 |
aftB | 4268146 | p.Tyr231His | missense_variant | 0.12 |
ethR | 4327018 | c.-531G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407936 | c.267T>A | synonymous_variant | 0.15 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |