Run ID: ERR4828782
Sample name:
Date: 01-04-2023 19:05:01
Number of reads: 1073263
Percentage reads mapped: 99.51
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.98 |
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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8189 | c.888G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759821 | c.15C>A | synonymous_variant | 0.17 |
rpoB | 762571 | p.Ile922Asn | missense_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776580 | p.Leu634Gln | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303291 | p.Thr121Pro | missense_variant | 0.12 |
Rv1258c | 1406618 | c.722delC | frameshift_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475673 | n.2021delA | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.1 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.1 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102393 | p.Ala217Val | missense_variant | 0.14 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 0.93 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.6 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.48 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519340 | p.Val409Ala | missense_variant | 0.2 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074582 | c.-111T>C | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568702 | c.-23C>A | upstream_gene_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
panD | 4044176 | p.Ala36Thr | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.14 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.14 |
embB | 4246613 | p.Gly34Arg | missense_variant | 0.12 |
ethR | 4327768 | p.Thr74Ala | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |