Run ID: ERR2229544
Sample name:
Date: 31-03-2023 17:18:09
Number of reads: 961522
Percentage reads mapped: 99.44
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 |
gyrA | 7459 | p.Arg53Leu | missense_variant | 0.17 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mshA | 576293 | c.948delC | frameshift_variant | 0.11 |
ccsA | 620007 | c.117T>A | synonymous_variant | 0.14 |
rpoB | 762353 | c.2547C>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.13 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.14 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.13 |
mmpL5 | 776172 | p.Asp770Val | missense_variant | 0.13 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.12 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.17 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304285 | p.Ala452Val | missense_variant | 0.17 |
fbiC | 1304465 | p.Gly512Val | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
rpsA | 1834117 | p.Glu192Asp | missense_variant | 0.17 |
tlyA | 1917893 | c.-47G>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918057 | p.Val40Leu | missense_variant | 0.18 |
tlyA | 1918168 | p.Phe77Leu | missense_variant | 0.2 |
katG | 2156387 | c.-276T>C | upstream_gene_variant | 0.12 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.37 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.16 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.15 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.15 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.46 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289800 | c.-559C>T | upstream_gene_variant | 0.15 |
ribD | 2987448 | p.Glu204* | stop_gained | 0.15 |
thyX | 3067221 | p.Ala242Glu | missense_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.18 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.2 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.19 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.16 |
embC | 4239752 | c.-111T>C | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242839 | p.Cys993Arg | missense_variant | 0.12 |
embA | 4243096 | c.-137A>C | upstream_gene_variant | 0.12 |
embA | 4243248 | p.Asn6Asp | missense_variant | 0.1 |
embA | 4244880 | p.Trp550Gly | missense_variant | 0.14 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.67 |
aftB | 4268769 | p.Gln23Leu | missense_variant | 0.13 |
ethR | 4328033 | p.Ala162Gly | missense_variant | 0.12 |
ethA | 4328469 | c.-996G>A | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |