Run ID: ERR11050546
Sample name:
Date: 03-04-2023 09:57:30
Number of reads: 3406895
Percentage reads mapped: 99.72
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575935 | c.588G>T | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.19 |
mshA | 576606 | p.Ala420Gly | missense_variant | 0.22 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.29 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.21 |
mmpL5 | 775626 | p.Trp952Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.35 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.14 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.43 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.21 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.3 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
alr | 3841608 | c.-188A>G | upstream_gene_variant | 1.0 |
rpoA | 3878589 | c.-82A>T | upstream_gene_variant | 0.15 |
rpoA | 3878590 | c.-83G>C | upstream_gene_variant | 0.18 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.2 |
rpoA | 3878608 | c.-101C>G | upstream_gene_variant | 0.4 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.5 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.6 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.89 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.39 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.25 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.27 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.21 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |