Run ID: SRR16088142
Sample name:
Date: 03-04-2023 16:04:16
Number of reads: 4387420
Percentage reads mapped: 99.51
Strain: lineage4.2.1
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.24 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.23 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.22 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.17 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.99 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.26 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517966 | c.-149G>A | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.22 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.12 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.19 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.54 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.25 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.34 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474213 | p.Lys69Asn | missense_variant | 0.17 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.42 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.28 |
rpoA | 3878590 | c.-83G>C | upstream_gene_variant | 0.18 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.5 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.63 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.33 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.26 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
aftB | 4268137 | c.700C>T | synonymous_variant | 1.0 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338205 | p.Val106Gly | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |