Run ID: SRR9588022
Sample name:
Date: 02-08-2023 15:35:04
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761076 | p.Phe424Leu | missense_variant | 0.15 | rifampicin |
rpoB | 761086 | p.Thr427Ile | missense_variant | 0.2 | rifampicin |
rpoB | 761277 | p.Ile491Phe | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289091 | p.His51Asp | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6053 | p.His272Tyr | missense_variant | 0.11 |
gyrB | 6406 | p.Asn389Lys | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9534 | c.2238_2240delCGG | disruptive_inframe_deletion | 0.12 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.1 |
rpoC | 766467 | p.Glu1033Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 1.0 |
mmpR5 | 779360 | p.Ala124Glu | missense_variant | 0.65 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781899 | p.Arg114Cys | missense_variant | 0.12 |
Rv1258c | 1407217 | p.Gly42Trp | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475635 | n.1978G>T | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.15 |
inhA | 1674605 | p.Leu135Gln | missense_variant | 0.14 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289860 | c.-619A>G | upstream_gene_variant | 0.13 |
kasA | 2518496 | c.382C>T | synonymous_variant | 1.0 |
kasA | 2518765 | c.651G>A | synonymous_variant | 0.12 |
folC | 2747450 | p.Ile50Thr | missense_variant | 0.11 |
Rv2752c | 3065023 | p.Pro390Leu | missense_variant | 1.0 |
thyX | 3067645 | p.Tyr101His | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448522 | p.Val7Phe | missense_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475339 | p.Ala445Ser | missense_variant | 0.22 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
fbiB | 3642198 | p.Val222Met | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |