Run ID: SRR6256995
Sample name:
Date: 04-04-2023 13:22:14
Number of reads: 692018
Percentage reads mapped: 99.55
Strain: lineage4.2.1.1
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 |
lineage4.2.1.1 | 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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4246734 | p.Leu74Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9243 | p.Ile648Phe | missense_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576164 | p.Arg273Ser | missense_variant | 0.17 |
mshA | 576387 | p.Ala347Val | missense_variant | 0.11 |
rpoC | 767155 | c.3786C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303750 | c.820T>C | synonymous_variant | 0.12 |
embR | 1417211 | p.Arg46Leu | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473777 | n.120T>A | non_coding_transcript_exon_variant | 0.11 |
inhA | 1673502 | c.-700C>A | upstream_gene_variant | 0.11 |
rpsA | 1834517 | p.Leu326Met | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168751 | p.Ser621Ile | missense_variant | 0.12 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714659 | p.Leu225Pro | missense_variant | 0.12 |
Rv2752c | 3065445 | c.747C>T | synonymous_variant | 0.12 |
thyA | 3073703 | p.Ile257Phe | missense_variant | 1.0 |
thyA | 3074495 | c.-24C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841040 | p.Asp127Glu | missense_variant | 0.11 |
rpoA | 3878440 | p.Ile23Thr | missense_variant | 0.14 |
clpC1 | 4038969 | p.Gln579Arg | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243130 | p.Pro1090Thr | missense_variant | 0.11 |
embA | 4245681 | p.Gly817Ser | missense_variant | 0.14 |
embB | 4246516 | c.3G>T | start_lost | 0.12 |
embB | 4246534 | p.Arg7Ser | missense_variant | 0.17 |
embB | 4246622 | p.Gly37Ser | missense_variant | 0.12 |
embB | 4247010 | c.500delC | frameshift_variant | 0.12 |
aftB | 4267232 | p.Asp535Glu | missense_variant | 0.14 |
aftB | 4269708 | c.-872C>A | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |