Run ID: ERR2229208
Sample name:
Date: 31-03-2023 16:48:42
Number of reads: 654319
Percentage reads mapped: 99.62
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.3 |
rpoB | 760892 | p.Asp362Glu | missense_variant | 0.17 |
rpoB | 760928 | c.1122G>A | synonymous_variant | 0.11 |
rpoC | 764057 | p.Ala230Thr | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417298 | p.Gly17Glu | missense_variant | 0.13 |
atpE | 1461108 | p.Ile22Leu | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.19 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.19 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.19 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.21 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.21 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.12 |
inhA | 1674459 | c.258C>T | synonymous_variant | 0.15 |
rpsA | 1834876 | c.1335G>A | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.11 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.12 |
PPE35 | 2170412 | c.201G>A | synonymous_variant | 0.29 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747154 | p.Met149Val | missense_variant | 0.11 |
Rv2752c | 3065193 | c.999C>A | synonymous_variant | 0.12 |
thyX | 3068001 | c.-56G>T | upstream_gene_variant | 0.15 |
fprA | 3474443 | p.Ser146* | stop_gained | 0.11 |
fprA | 3474592 | p.Ile196Phe | missense_variant | 0.14 |
fprA | 3475166 | p.Gly387Val | missense_variant | 0.12 |
Rv3236c | 3612437 | p.Leu227Ser | missense_variant | 0.1 |
clpC1 | 4039561 | p.Ala382Ser | missense_variant | 0.15 |
embC | 4242264 | p.Glu801Gly | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245722 | c.-792C>T | upstream_gene_variant | 0.11 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.19 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.19 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.19 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407752 | p.Pro151Ser | missense_variant | 0.12 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |