Run ID: ERR4817455
Sample name:
Date: 01-04-2023 15:00:04
Number of reads: 826684
Percentage reads mapped: 99.53
Strain: lineage4.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7935 | p.Glu212Lys | missense_variant | 0.15 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490988 | p.Leu69Pro | missense_variant | 0.12 |
fgd1 | 491523 | c.745delT | frameshift_variant | 0.11 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779465 | p.Gln159Arg | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304422 | p.Ala498Thr | missense_variant | 0.11 |
embR | 1416806 | p.Glu181Gly | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834734 | p.Ala398Val | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918164 | c.225G>A | synonymous_variant | 1.0 |
katG | 2155914 | c.198G>A | synonymous_variant | 0.14 |
PPE35 | 2167766 | c.2847C>G | synonymous_variant | 0.15 |
PPE35 | 2169738 | p.Thr292Ile | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289657 | c.-416G>T | upstream_gene_variant | 0.15 |
kasA | 2518227 | p.Ala38Asp | missense_variant | 0.15 |
ahpC | 2726571 | p.Ala127Thr | missense_variant | 0.12 |
folC | 2747186 | p.Ser138Leu | missense_variant | 0.14 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
thyA | 3073754 | p.Glu240Gln | missense_variant | 0.11 |
thyA | 3073877 | p.Phe199Leu | missense_variant | 0.17 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640352 | c.-191G>A | upstream_gene_variant | 0.12 |
clpC1 | 4039797 | p.Asp303Gly | missense_variant | 0.14 |
panD | 4044039 | c.243G>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243461 | p.Ser77Pro | missense_variant | 1.0 |
embB | 4249474 | c.2961C>T | synonymous_variant | 0.11 |
aftB | 4269060 | c.-224G>T | upstream_gene_variant | 0.12 |
ethA | 4326454 | c.1020C>T | synonymous_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |