Run ID: SRR1173201
Sample name:
Date: 03-04-2023 03:18:58
Number of reads: 821253
Percentage reads mapped: 97.53
Strain: lineage4.3.3
Drug-resistance: MDR-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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Trp | missense_variant | 0.94 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
ethA | 4327484 | c.-11A>G | upstream_gene_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 491207 | p.Leu142Pro | missense_variant | 0.11 |
mshA | 575998 | c.651C>T | synonymous_variant | 0.25 |
ccsA | 620830 | p.Thr314Ser | missense_variant | 0.11 |
rpoB | 761032 | p.Gln409Arg | missense_variant | 0.95 |
rpoB | 761467 | p.Leu554Pro | missense_variant | 1.0 |
rpoB | 763216 | p.Ala1137Val | missense_variant | 0.1 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778921 | c.-441G>T | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.11 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.11 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.97 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156011 | p.Gly34Glu | missense_variant | 0.1 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.38 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2714355 | c.978C>T | synonymous_variant | 0.18 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612488 | c.628delG | frameshift_variant | 0.12 |
alr | 3840359 | c.1062G>T | synonymous_variant | 0.12 |
rpoA | 3878555 | c.-48G>T | upstream_gene_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038755 | c.1950G>A | synonymous_variant | 0.13 |
embC | 4239863 | c.1A>G | start_lost | 1.0 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4269549 | c.-713C>T | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
pncA | 2288947 | c.-606_294del | start_lost&conservative_inframe_deletion | 1.0 |
gid | 4407912 | c.160_290del | frameshift_variant | 1.0 |