Run ID: SRR3732645
Sample name:
Date: 04-04-2023 05:36:58
Number of reads: 1647826
Percentage reads mapped: 99.53
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.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289231 | p.Leu4Ser | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | 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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8774 | c.1473C>T | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620123 | p.Arg78Leu | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765463 | p.Asn698Lys | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777587 | c.894G>A | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472724 | n.879G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473275 | n.1430C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473920 | n.263G>T | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.14 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.12 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.12 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.17 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.17 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.14 |
PPE35 | 2170142 | c.471G>C | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289545 | c.-304T>C | upstream_gene_variant | 0.11 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2715581 | c.-249C>A | upstream_gene_variant | 0.15 |
pepQ | 2859863 | p.Asp186Tyr | missense_variant | 0.13 |
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 | 3641958 | p.Val142Ile | missense_variant | 0.18 |
fbiB | 3642648 | p.Met372Val | missense_variant | 0.1 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038392 | c.2312delG | frameshift_variant | 0.12 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.12 |
embC | 4240275 | p.Pro138Leu | missense_variant | 0.12 |
embC | 4241693 | p.Ala611Thr | missense_variant | 0.18 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embC | 4242366 | p.Ser835Tyr | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Arg | missense_variant | 0.11 |
embA | 4244839 | p.Leu536Pro | missense_variant | 0.15 |
embA | 4245915 | p.Gln895* | stop_gained | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407973 | p.Val77Gly | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |