Run ID: ERR7361969
Sample name:
Date: 02-04-2023 04:14:36
Number of reads: 1604855
Percentage reads mapped: 99.71
Strain: lineage4.8
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288719 | p.Met175Val | missense_variant | 1.0 | pyrazinamide |
alr | 3840393 | p.Met343Thr | missense_variant | 1.0 | cycloserine |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5809 | c.570C>T | synonymous_variant | 0.17 |
gyrB | 6464 | p.Lys409Glu | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 760001 | c.195C>A | synonymous_variant | 0.22 |
rpoB | 760035 | p.Val77Met | missense_variant | 0.15 |
rpoC | 763494 | p.Glu42Gly | missense_variant | 0.22 |
rpoC | 763796 | p.Met143Val | missense_variant | 0.11 |
rpoC | 764014 | c.645G>A | synonymous_variant | 0.13 |
rpoC | 765797 | p.Asn810Asp | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781912 | p.Gly118Val | missense_variant | 0.13 |
rplC | 800929 | p.Thr41Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471843 | n.-3G>T | upstream_gene_variant | 1.0 |
rrs | 1472609 | n.764G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474391 | n.734G>T | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674463 | p.Leu88Phe | missense_variant | 0.15 |
rpsA | 1833489 | c.-53T>A | upstream_gene_variant | 0.17 |
rpsA | 1834132 | c.591G>A | synonymous_variant | 0.22 |
rpsA | 1834270 | c.729G>A | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154240 | p.Met624Ile | missense_variant | 0.17 |
katG | 2155605 | c.507C>A | synonymous_variant | 0.15 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169122 | c.1491C>G | synonymous_variant | 0.15 |
PPE35 | 2169149 | c.1464G>C | synonymous_variant | 1.0 |
PPE35 | 2169345 | p.Asn423Ser | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288949 | p.Ala98Val | missense_variant | 1.0 |
pncA | 2289608 | c.-367A>G | upstream_gene_variant | 0.2 |
kasA | 2518106 | c.-9C>A | upstream_gene_variant | 0.15 |
pepQ | 2860337 | p.Ile28Leu | missense_variant | 0.17 |
thyX | 3067720 | p.Ala76Thr | missense_variant | 0.12 |
fbiB | 3642835 | p.Gly434Glu | missense_variant | 0.12 |
rpoA | 3877486 | p.Tyr341Cys | missense_variant | 0.1 |
rpoA | 3878531 | c.-25delG | upstream_gene_variant | 0.25 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
panD | 4044285 | c.-4A>G | upstream_gene_variant | 0.29 |
embC | 4242097 | c.2237delG | frameshift_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ubiA | 4269518 | p.Ala106Pro | missense_variant | 0.1 |
ethR | 4327123 | c.-426G>A | upstream_gene_variant | 0.12 |
ethR | 4327465 | c.-84C>T | upstream_gene_variant | 0.22 |
ethA | 4327545 | c.-72G>A | upstream_gene_variant | 0.12 |
ethR | 4327907 | p.Val120Glu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
ethA | 4326539 | c.866_934delNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNT | disruptive_inframe_deletion | 1.0 |