Run ID: SRR4037854
Sample name:
Date: 04-04-2023 07:43:13
Number of reads: 465508
Percentage reads mapped: 99.59
Strain: lineage4.3.2.1
Drug-resistance: Other
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 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326609 | c.864delC | frameshift_variant | 0.17 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7799 | c.498A>C | synonymous_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9760 | p.Glu820Val | missense_variant | 0.4 |
rpoB | 762486 | p.Pro894Ser | missense_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766881 | p.Gly1171Asp | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777634 | p.Gly283Ser | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472174 | n.329C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472857 | n.1012A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474795 | n.1138A>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834462 | c.921C>T | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.17 |
Rv1979c | 2221735 | p.Arg477Gln | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518955 | p.Ala281Thr | missense_variant | 0.33 |
thyX | 3067931 | c.15G>A | synonymous_variant | 0.29 |
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 |
fbiB | 3641681 | c.147C>T | synonymous_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4241436 | p.Ala525Asp | missense_variant | 0.4 |
embC | 4241689 | c.1827G>T | synonymous_variant | 0.15 |
embC | 4242320 | p.Pro820Ser | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242901 | c.-332G>T | upstream_gene_variant | 0.13 |
embB | 4248009 | p.Leu499Pro | missense_variant | 0.18 |
aftB | 4268030 | c.807G>A | synonymous_variant | 0.22 |
ubiA | 4269870 | c.-37C>T | upstream_gene_variant | 0.33 |
ethA | 4326629 | p.Phe282Ser | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |