Run ID: ERR11068817
Sample name:
Date: 07-04-2023 02:54:25
Number of reads: 3762034
Percentage reads mapped: 99.48
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 | 6438 | p.Pro400Arg | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619975 | c.85C>T | synonymous_variant | 0.29 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 762725 | c.-645C>G | upstream_gene_variant | 0.18 |
rpoC | 764545 | c.1176C>T | synonymous_variant | 0.25 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777337 | p.Val382Ile | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801235 | p.Ala143Thr | missense_variant | 0.14 |
fbiC | 1304379 | c.1449G>T | synonymous_variant | 0.11 |
fbiC | 1304401 | p.Ile491Phe | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673572 | p.Thr45Pro | missense_variant | 0.12 |
inhA | 1674363 | c.162G>A | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918072 | p.Ala45Thr | missense_variant | 0.2 |
tlyA | 1918132 | p.Arg65Ser | missense_variant | 0.12 |
ndh | 2102275 | c.768C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
pepQ | 2859606 | c.813G>T | synonymous_variant | 0.17 |
thyX | 3067288 | p.Ala220Thr | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087831 | p.Ala338Thr | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474899 | p.Gly298Asp | missense_variant | 0.12 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.29 |
fbiB | 3642046 | p.Ala171Val | missense_variant | 0.11 |
fbiB | 3642236 | c.702G>A | synonymous_variant | 0.33 |
fbiB | 3642812 | c.1278C>T | synonymous_variant | 0.18 |
embC | 4240421 | p.Glu187* | stop_gained | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245459 | p.Pro743Ser | missense_variant | 0.2 |
embA | 4245676 | p.Gly815Glu | missense_variant | 0.1 |
ethA | 4328044 | c.-571G>A | upstream_gene_variant | 0.18 |
whiB6 | 4338207 | c.315G>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |