Run ID: SRR6896346
Sample name:
Date: 04-04-2023 18:03:08
Number of reads: 513326
Percentage reads mapped: 99.55
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 0.42 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7580 | c.279C>T | synonymous_variant | 0.55 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8086 | p.Asp262Val | missense_variant | 0.3 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.75 |
mshA | 575164 | c.-184T>A | upstream_gene_variant | 0.11 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.86 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.72 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407344 | c.-4A>G | upstream_gene_variant | 0.1 |
embR | 1417140 | p.Ala70Ser | missense_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473847 | n.190G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473926 | n.269G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474739 | n.1082G>T | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 0.3 |
inhA | 1674498 | c.297G>C | synonymous_variant | 0.79 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918451 | p.Ala171Asp | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289843 | c.-602T>C | upstream_gene_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.66 |
folC | 2747022 | p.Val193Ile | missense_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 0.33 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 0.27 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4242838 | c.-395C>T | upstream_gene_variant | 0.17 |
embA | 4244581 | p.Asp450Val | missense_variant | 0.12 |
embA | 4245344 | c.2112G>A | synonymous_variant | 0.15 |
embB | 4249428 | p.Arg972Leu | missense_variant | 0.12 |
embB | 4249709 | p.Lys1066Glu | missense_variant | 0.29 |
aftB | 4268238 | p.Met200Thr | missense_variant | 0.12 |
aftB | 4268861 | c.-25T>C | upstream_gene_variant | 0.35 |
aftB | 4269129 | c.-293G>A | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |