Run ID: SRR19428566
Sample name:
Date: 03-04-2023 21:40:31
Number of reads: 1306356
Percentage reads mapped: 99.76
Strain: lineage4.3.4.2.1
Drug-resistance: Other
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 | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247728 | p.Glu405Asp | missense_variant | 0.22 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8795 | c.1494C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491305 | p.Ala175Ser | missense_variant | 0.22 |
mshA | 575314 | c.-34C>A | upstream_gene_variant | 0.5 |
mshA | 575869 | c.522G>T | synonymous_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779609 | c.-704C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303996 | p.Gly356Ser | missense_variant | 0.4 |
Rv1258c | 1407170 | p.Phe57Leu | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834963 | c.1422G>T | synonymous_variant | 0.29 |
rpsA | 1834977 | p.Gly479Val | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170101 | p.Pro171Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289909 | c.-668G>A | upstream_gene_variant | 1.0 |
kasA | 2519164 | c.1050C>T | synonymous_variant | 0.18 |
folC | 2746571 | p.Arg343Leu | missense_variant | 0.14 |
folC | 2747726 | c.-128G>T | upstream_gene_variant | 0.11 |
pepQ | 2860191 | p.Glu76Asp | missense_variant | 0.22 |
ribD | 2987337 | p.Gly167Ser | missense_variant | 0.14 |
Rv2752c | 3067139 | c.-948G>T | upstream_gene_variant | 0.14 |
thyX | 3067275 | p.Pro224His | missense_variant | 0.33 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087333 | p.Val172Met | missense_variant | 0.4 |
fbiD | 3339337 | p.Gly74Trp | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiB | 3642065 | c.531C>A | synonymous_variant | 0.14 |
fbiB | 3642207 | p.Asp225Tyr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4241159 | p.Ala433Ser | missense_variant | 0.14 |
embC | 4241167 | c.1305C>A | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243857 | p.Leu209Ile | missense_variant | 0.14 |
embA | 4244169 | p.Gln313Lys | missense_variant | 0.12 |
embA | 4244254 | p.Arg341Leu | missense_variant | 0.29 |
embA | 4244353 | p.Pro374Gln | missense_variant | 0.12 |
embA | 4245745 | p.Pro838Gln | missense_variant | 0.2 |
embB | 4247658 | p.Pro382His | missense_variant | 0.22 |
aftB | 4267655 | c.1182C>T | synonymous_variant | 0.13 |
aftB | 4267710 | p.Ser376Ile | missense_variant | 0.11 |
ethR | 4328021 | p.Asp158Gly | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |