Run ID: SRR10272562
Sample name:
Date: 02-04-2023 16:41:39
Number of reads: 974107
Percentage reads mapped: 86.11
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 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.36 |
rpoB | 761022 | p.Ile406Phe | missense_variant | 0.12 |
rpoB | 761715 | p.Val637Ile | missense_variant | 0.14 |
rpoC | 764540 | p.Val391Phe | missense_variant | 0.12 |
rpoC | 766061 | p.Val898Ile | missense_variant | 0.12 |
rpoC | 766064 | p.Val899Ile | missense_variant | 0.12 |
rpoC | 766076 | p.Glu903Gln | missense_variant | 0.13 |
rpoC | 766080 | p.Arg904Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800696 | c.-113C>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674870 | p.Asp223Glu | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918001 | p.Gln21Arg | missense_variant | 0.29 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169125 | p.Val496Ile | missense_variant | 0.17 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.47 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.48 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518348 | c.234A>T | synonymous_variant | 0.11 |
kasA | 2518801 | c.687G>A | synonymous_variant | 0.22 |
pepQ | 2859399 | c.1020C>T | synonymous_variant | 0.12 |
ribD | 2987404 | p.Arg189Leu | missense_variant | 0.12 |
thyA | 3074654 | c.-183T>G | upstream_gene_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448412 | c.-92G>A | upstream_gene_variant | 0.18 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3448654 | p.Pro51Ala | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612155 | p.Arg321Leu | missense_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.13 |
embC | 4242401 | p.Arg847Ser | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.23 |
embA | 4243540 | p.Ala103Val | missense_variant | 0.18 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.22 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.24 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407534 | c.669G>A | synonymous_variant | 0.14 |
gid | 4408115 | p.Gly30Cys | missense_variant | 0.13 |