Run ID: ERR2229257
Sample name:
Date: 31-03-2023 16:53:11
Number of reads: 1100668
Percentage reads mapped: 99.06
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 |
mshA | 575584 | c.237G>T | synonymous_variant | 0.14 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.14 |
rpoB | 761469 | p.Val555Ile | missense_variant | 0.14 |
rpoC | 763507 | c.138G>T | synonymous_variant | 0.13 |
rpoC | 764663 | p.Val432Ile | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775863 | p.Ala873Glu | missense_variant | 0.17 |
mmpL5 | 775885 | p.Ile866Phe | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800676 | c.-133C>A | upstream_gene_variant | 0.13 |
rplC | 801166 | p.Gly120Arg | missense_variant | 0.11 |
fbiC | 1303720 | p.Gly264Cys | missense_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.13 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
fabG1 | 1674152 | p.Pro238Gln | missense_variant | 0.17 |
inhA | 1674309 | c.108G>T | synonymous_variant | 0.18 |
inhA | 1674832 | p.Ala211Ser | missense_variant | 0.15 |
rpsA | 1834942 | p.Asp467Glu | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.2 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.24 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.29 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.21 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.38 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.37 |
Rv1979c | 2223201 | c.-38delG | upstream_gene_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288977 | p.Ala89Ser | missense_variant | 0.13 |
kasA | 2519293 | p.Asp393Glu | missense_variant | 0.2 |
eis | 2714323 | p.Arg337His | missense_variant | 0.14 |
folC | 2746646 | p.Gln318Arg | missense_variant | 0.17 |
folC | 2746813 | c.786A>G | synonymous_variant | 0.11 |
folC | 2747755 | c.-157C>T | upstream_gene_variant | 0.13 |
ribD | 2987206 | p.Ser123Tyr | missense_variant | 0.22 |
Rv2752c | 3065227 | c.964delG | frameshift_variant | 0.25 |
thyX | 3067625 | c.321C>A | synonymous_variant | 0.12 |
fbiD | 3339666 | c.549G>T | synonymous_variant | 0.25 |
fprA | 3474497 | p.Arg164Gln | missense_variant | 0.15 |
alr | 3840787 | p.Ala212Ser | missense_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.38 |
clpC1 | 4038482 | p.Gln741His | missense_variant | 0.18 |
embC | 4239800 | c.-63T>G | upstream_gene_variant | 0.2 |
embC | 4240219 | c.357C>A | synonymous_variant | 0.12 |
embC | 4241744 | p.Phe628Leu | missense_variant | 0.2 |
embC | 4242065 | p.Ser735Ala | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.33 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.33 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.22 |
ethA | 4326014 | p.Val487Gly | missense_variant | 0.18 |
ethR | 4327844 | p.Arg99Leu | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |