Run ID: ERR2229655
Sample name:
Date: 31-03-2023 17:23:49
Number of reads: 506608
Percentage reads mapped: 99.15
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 |
---|---|---|---|---|---|
embC | 4240748 | p.Tyr296His | missense_variant | 0.12 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7068 | p.Tyr610Phe | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8500 | p.Ala400Glu | missense_variant | 0.18 |
gyrA | 9710 | p.Leu803Phe | missense_variant | 0.12 |
mshA | 575893 | c.546C>T | synonymous_variant | 0.29 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
ccsA | 620608 | p.Phe240Leu | missense_variant | 0.12 |
rpoB | 761869 | p.Asp688Val | missense_variant | 0.12 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.12 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.15 |
rpoB | 762691 | p.Pro962Leu | missense_variant | 0.25 |
rpoB | 762852 | p.Pro1016Thr | missense_variant | 0.18 |
rpoC | 764914 | p.Met515Ile | missense_variant | 0.13 |
rpoC | 765863 | p.Ile832Leu | missense_variant | 0.22 |
rpoC | 766673 | p.Gly1102Ser | missense_variant | 0.22 |
rpoC | 767253 | p.Pro1295Gln | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777179 | c.1302G>A | synonymous_variant | 0.2 |
mmpL5 | 777767 | c.714C>T | synonymous_variant | 0.18 |
mmpR5 | 779366 | p.Gly126Val | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801391 | p.Lys195* | stop_gained | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417130 | p.His73Leu | missense_variant | 0.12 |
atpE | 1461208 | p.Ile55Asn | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473789 | n.132G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674808 | p.Val203Ile | missense_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.14 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169596 | p.Phe339Trp | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.54 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.53 |
PPE35 | 2170412 | c.201G>C | synonymous_variant | 0.13 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518759 | c.645C>A | synonymous_variant | 0.18 |
folC | 2747465 | p.Pro45Leu | missense_variant | 0.17 |
ribD | 2987365 | p.Ala176Glu | missense_variant | 0.15 |
thyX | 3068153 | c.-208G>A | upstream_gene_variant | 0.11 |
thyA | 3073848 | c.624C>A | synonymous_variant | 0.12 |
ald | 3086839 | p.Thr7Ile | missense_variant | 0.11 |
ald | 3087359 | c.540C>T | synonymous_variant | 0.14 |
fbiD | 3339324 | c.207G>C | synonymous_variant | 0.13 |
Rv3083 | 3448356 | c.-148G>A | upstream_gene_variant | 0.13 |
whiB7 | 3568633 | p.Pro16Arg | missense_variant | 0.15 |
Rv3236c | 3613192 | c.-76G>C | upstream_gene_variant | 0.12 |
fbiB | 3642710 | c.1176G>T | synonymous_variant | 0.22 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.29 |
rpoA | 3877529 | p.Thr327Ser | missense_variant | 0.12 |
rpoA | 3877790 | p.Glu240* | stop_gained | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.23 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.27 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.27 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.25 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.33 |
embB | 4247041 | p.Phe176Leu | missense_variant | 0.4 |
ethA | 4326476 | p.Leu333Pro | missense_variant | 0.12 |
ethR | 4327735 | p.Phe63Leu | missense_variant | 0.25 |
ethA | 4327749 | c.-276G>T | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |