Run ID: SRR4034160
Sample name:
Date: 04-04-2023 06:36:18
Number of reads: 1210915
Percentage reads mapped: 99.79
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 | 2153990 | c.2121delT | frameshift_variant | 0.14 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5256 | p.Lys6Arg | missense_variant | 0.1 |
gyrB | 5477 | p.Asp80Asn | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.93 |
gyrA | 9077 | c.1776C>T | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761564 | c.1758G>T | synonymous_variant | 0.11 |
rpoC | 762473 | c.-897C>A | upstream_gene_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.95 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775926 | c.2554delC | frameshift_variant | 0.25 |
mmpL5 | 777218 | c.1263G>A | synonymous_variant | 0.12 |
mmpR5 | 778313 | c.-677G>T | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302869 | c.-62G>A | upstream_gene_variant | 0.11 |
fbiC | 1304037 | c.1107G>A | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833783 | p.Ser81Phe | missense_variant | 0.13 |
tlyA | 1917917 | c.-23G>A | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102412 | p.Val211Met | missense_variant | 0.1 |
PPE35 | 2170400 | c.212delC | frameshift_variant | 0.17 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223096 | c.69G>A | synonymous_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2715416 | c.-84C>A | upstream_gene_variant | 0.11 |
eis | 2715506 | c.-175delG | upstream_gene_variant | 0.17 |
ahpC | 2726313 | p.Asp41Tyr | missense_variant | 0.1 |
folC | 2747532 | p.Glu23Lys | missense_variant | 0.12 |
ribD | 2987107 | p.Ile90Thr | missense_variant | 0.15 |
ribD | 2987580 | p.Ser248Thr | missense_variant | 0.33 |
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 |
Rv3083 | 3449062 | p.Ala187Ser | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641508 | c.969delG | frameshift_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039575 | p.Ala377Val | missense_variant | 0.12 |
clpC1 | 4039683 | p.Arg341His | missense_variant | 0.11 |
clpC1 | 4040257 | p.Ala150Thr | missense_variant | 0.22 |
embC | 4239850 | c.-13A>G | upstream_gene_variant | 0.15 |
embC | 4240067 | c.208_209delGT | frameshift_variant | 0.12 |
embC | 4241712 | p.Arg617Gln | missense_variant | 0.12 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.33 |
embC | 4242579 | p.Ala906Val | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245475 | p.Gly748Asp | missense_variant | 0.13 |
embB | 4249661 | p.Ala1050Thr | missense_variant | 0.13 |
embB | 4249787 | p.Gly1092Ser | missense_variant | 0.11 |
aftB | 4268775 | p.Ser21Asn | missense_variant | 0.11 |
aftB | 4268913 | c.-77A>T | upstream_gene_variant | 0.12 |
ethR | 4326787 | c.-762C>A | upstream_gene_variant | 0.12 |
ethA | 4328291 | c.-818C>A | upstream_gene_variant | 0.11 |
ethA | 4328318 | c.-845G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |