Run ID: SRR6832116
Sample name:
Date: 04-04-2023 17:14:13
Number of reads: 637424
Percentage reads mapped: 99.64
Strain: lineage4.3.3
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155959 | c.152delA | frameshift_variant | 0.25 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5922 | p.Glu228Gly | missense_variant | 0.25 |
gyrB | 7058 | p.Ile607Val | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491036 | p.Val85Gly | missense_variant | 0.29 |
rpoB | 762958 | p.Leu1051Pro | missense_variant | 0.15 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.22 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474954 | n.1297A>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102117 | p.Leu309Arg | missense_variant | 0.29 |
ndh | 2102563 | c.480G>T | synonymous_variant | 0.16 |
katG | 2154515 | p.Pro533Thr | missense_variant | 0.33 |
katG | 2155732 | p.Gln127Ser | missense_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167737 | p.Leu959Pro | missense_variant | 0.33 |
PPE35 | 2168979 | p.Pro545Leu | missense_variant | 0.25 |
Rv1979c | 2223119 | p.Phe16Leu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
folC | 2747461 | c.138C>T | synonymous_variant | 0.12 |
ribD | 2986794 | c.-45G>A | upstream_gene_variant | 0.12 |
ribD | 2986938 | p.Tyr34Asn | missense_variant | 0.2 |
Rv2752c | 3065119 | p.Ile358Thr | missense_variant | 0.15 |
thyX | 3067351 | p.Arg199Trp | missense_variant | 0.29 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086815 | c.-5T>G | upstream_gene_variant | 0.27 |
Rv3083 | 3449931 | c.1428C>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841447 | c.-27A>G | upstream_gene_variant | 0.15 |
rpoA | 3877653 | c.855C>T | synonymous_variant | 0.14 |
ddn | 3987204 | c.363delA | frameshift_variant | 0.29 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243013 | p.Asp1051Tyr | missense_variant | 0.33 |
embA | 4243824 | p.Thr198Ala | missense_variant | 0.29 |
embA | 4246173 | p.Ile981Phe | missense_variant | 0.25 |
aftB | 4268566 | p.Ser91Ala | missense_variant | 1.0 |
ethA | 4328459 | c.-986A>G | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |