Run ID: SRR4034671
Sample name:
Date: 04-04-2023 06:57:48
Number of reads: 804394
Percentage reads mapped: 99.51
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 | 2154659 | c.1452delT | frameshift_variant | 0.17 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5878 | c.639G>A | synonymous_variant | 0.14 |
gyrB | 6783 | p.Asp515Gly | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8397 | p.Val366Ile | missense_variant | 0.12 |
gyrA | 8555 | c.1254G>A | synonymous_variant | 0.11 |
gyrA | 8963 | c.1662C>T | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575380 | c.33G>A | synonymous_variant | 0.18 |
rpoB | 759747 | c.-60C>A | upstream_gene_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 763353 | c.-17_-16insG | upstream_gene_variant | 0.13 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775811 | c.2669delT | frameshift_variant | 0.17 |
mmpL5 | 776319 | p.Ser721Thr | missense_variant | 0.11 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781576 | p.Gln6Arg | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472116 | n.273delA | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472319 | n.478_481delAGGT | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474781 | n.1124C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154072 | c.2040C>G | synonymous_variant | 0.12 |
katG | 2154488 | p.Asp542Asn | missense_variant | 0.14 |
PPE35 | 2167692 | p.Gly974Val | missense_variant | 0.2 |
PPE35 | 2168252 | c.2361G>A | synonymous_variant | 0.14 |
PPE35 | 2170503 | c.109dupG | frameshift_variant | 0.18 |
Rv1979c | 2221980 | c.1185A>G | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289080 | c.162G>T | synonymous_variant | 0.12 |
pncA | 2290209 | c.-969delG | upstream_gene_variant | 0.29 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2726681 | c.491_492dupTG | frameshift_variant | 0.25 |
thyA | 3074018 | p.Phe152Leu | missense_variant | 0.12 |
thyA | 3074027 | p.Phe149Ile | missense_variant | 0.12 |
thyA | 3074035 | p.Cys146Ser | missense_variant | 0.12 |
thyA | 3074060 | p.Ile138Phe | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087308 | c.489G>T | synonymous_variant | 0.13 |
fbiD | 3339304 | p.Thr63Pro | missense_variant | 0.4 |
Rv3083 | 3448310 | c.-194G>A | upstream_gene_variant | 0.29 |
Rv3083 | 3449274 | c.771C>A | synonymous_variant | 0.11 |
Rv3083 | 3449690 | p.Thr396Asn | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612470 | p.Glu216Gly | missense_variant | 0.15 |
fbiA | 3640531 | c.-12C>T | upstream_gene_variant | 0.25 |
fbiB | 3641672 | c.138G>T | synonymous_variant | 0.15 |
embC | 4240950 | p.Val363Ala | missense_variant | 0.29 |
embC | 4242049 | c.2187C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246292 | c.-222A>C | upstream_gene_variant | 0.11 |
embB | 4248138 | p.Gly542Asp | missense_variant | 0.14 |
aftB | 4268226 | p.Ala204Gly | missense_variant | 0.11 |
aftB | 4268324 | c.512delT | frameshift_variant | 0.12 |
ethA | 4327263 | p.Gly71Arg | missense_variant | 0.11 |
ethA | 4328423 | c.-950T>C | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338699 | c.-179delT | upstream_gene_variant | 0.33 |
gid | 4407986 | p.Gly73Arg | missense_variant | 0.14 |