Run ID: ERR11081282
Sample name:
Date: 08-04-2023 14:37:07
Number of reads: 557174
Percentage reads mapped: 99.55
Strain: lineage4.5
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 |
lineage4.5 | Euro-American | H;T | RD122 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.96 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491003 | p.Val74Ala | missense_variant | 0.12 |
fgd1 | 491030 | p.Pro83His | missense_variant | 0.12 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.18 |
ccsA | 619788 | c.-103G>T | upstream_gene_variant | 1.0 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
rpoC | 764996 | p.Val543Met | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406101 | p.Pro414Ser | missense_variant | 1.0 |
Rv1258c | 1406536 | p.Gly269Ser | missense_variant | 0.12 |
embR | 1416662 | p.Arg229His | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154533 | p.Ser527Ala | missense_variant | 0.12 |
PPE35 | 2168575 | p.Ala680Thr | missense_variant | 0.12 |
PPE35 | 2170333 | c.277_279delATG | conservative_inframe_deletion | 0.12 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289312 | c.-71G>A | upstream_gene_variant | 0.11 |
ahpC | 2726549 | c.357C>T | synonymous_variant | 0.11 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.12 |
thyX | 3067587 | p.Pro120Leu | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640850 | p.Glu103Gly | missense_variant | 0.11 |
fbiA | 3641453 | p.Arg304Gln | missense_variant | 0.17 |
fbiB | 3641700 | p.Cys56Arg | missense_variant | 0.11 |
fbiB | 3641715 | p.Val61Phe | missense_variant | 0.12 |
rpoA | 3877842 | c.666A>T | synonymous_variant | 0.12 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244409 | p.Trp393Arg | missense_variant | 0.11 |
aftB | 4267735 | p.Gly368Ser | missense_variant | 0.12 |
aftB | 4268279 | c.558G>A | synonymous_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |