Run ID: SRR6896337
Sample name:
Date: 04-04-2023 18:02:53
Number of reads: 645080
Percentage reads mapped: 99.5
Strain: lineage4.4.2
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 |
lineage4.4.2 | Euro-American | T1;T2 | 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 |
rpoC | 764459 | p.Glu364Lys | missense_variant | 0.14 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.1 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777126 | p.Ser452Ile | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304973 | c.2043C>A | synonymous_variant | 0.13 |
fbiC | 1305015 | c.2085G>A | synonymous_variant | 0.18 |
Rv1258c | 1406442 | p.Leu300Ser | missense_variant | 0.13 |
Rv1258c | 1406503 | p.Val280Leu | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155630 | p.Trp161Leu | missense_variant | 0.15 |
PPE35 | 2167727 | c.2886C>T | synonymous_variant | 0.11 |
PPE35 | 2168389 | p.Gln742Lys | missense_variant | 0.13 |
PPE35 | 2168578 | p.Phe679Leu | missense_variant | 0.11 |
PPE35 | 2168757 | p.Gln619Arg | missense_variant | 1.0 |
PPE35 | 2170143 | p.Gly157Val | missense_variant | 0.12 |
PPE35 | 2170579 | p.Ser12Pro | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746681 | c.918C>A | synonymous_variant | 0.13 |
folC | 2747171 | p.Gly143Asp | missense_variant | 0.1 |
ribD | 2987500 | p.Gly221Ala | missense_variant | 0.11 |
Rv2752c | 3065681 | p.Ile171Val | missense_variant | 0.14 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612286 | c.830delG | frameshift_variant | 0.15 |
Rv3236c | 3612568 | c.549G>A | synonymous_variant | 0.12 |
alr | 3840212 | c.1209C>T | synonymous_variant | 1.0 |
rpoA | 3878553 | c.-46C>G | upstream_gene_variant | 0.5 |
clpC1 | 4038198 | p.Gly836Glu | missense_variant | 0.11 |
embC | 4242316 | p.Ser818Arg | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243531 | p.Thr100Ser | missense_variant | 0.17 |
embA | 4244862 | p.Leu544Met | missense_variant | 0.33 |
embA | 4245807 | p.Leu859Val | missense_variant | 0.18 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
embB | 4246856 | c.352_354delGTC | conservative_inframe_deletion | 0.1 |
embB | 4247249 | p.Gly246Arg | missense_variant | 1.0 |
embB | 4249434 | p.Leu974Gln | missense_variant | 0.12 |
aftB | 4268011 | c.820_825delGTGCCG | conservative_inframe_deletion | 0.12 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
ubiA | 4269542 | p.Pro98Thr | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408251 | c.-49T>A | upstream_gene_variant | 0.11 |