Run ID: SRR6045241
Sample name:
Date: 04-04-2023 11:55:19
Number of reads: 407533
Percentage reads mapped: 91.59
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6449 | p.Lys404Glu | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7425 | p.Pro42Ser | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8503 | p.Leu401Pro | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.29 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575766 | p.Glu140Val | missense_variant | 0.2 |
mshA | 576744 | p.Val466Gly | missense_variant | 0.25 |
ccsA | 620836 | p.Gly316Cys | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.25 |
rpoB | 760106 | c.300G>A | synonymous_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761278 | p.Ile491Asn | missense_variant | 0.2 |
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 | 1406189 | c.1152A>G | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918185 | c.246G>A | synonymous_variant | 0.15 |
katG | 2156410 | c.-299T>C | upstream_gene_variant | 0.15 |
PPE35 | 2169827 | c.786G>A | synonymous_variant | 1.0 |
PPE35 | 2169984 | p.Ala210Val | missense_variant | 0.18 |
Rv1979c | 2221879 | p.Ala429Val | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289566 | c.-325G>A | upstream_gene_variant | 0.18 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339650 | p.Leu178Pro | missense_variant | 0.25 |
Rv3083 | 3449033 | p.Gly177Asp | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3640869 | c.-666G>T | upstream_gene_variant | 0.2 |
fbiA | 3641394 | p.Ile284Met | missense_variant | 0.18 |
fbiB | 3641454 | c.-81G>A | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4247174 | p.Ala221Thr | missense_variant | 0.14 |
embB | 4247497 | p.Asp328Glu | missense_variant | 0.22 |
embB | 4249467 | p.Leu985Pro | missense_variant | 0.2 |
aftB | 4267635 | p.Arg401Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |