Run ID: ERR2229595
Sample name:
Date: 31-03-2023 17:21:58
Number of reads: 1536882
Percentage reads mapped: 99.42
Strain: lineage4.8
Drug-resistance: RR-TB
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 |
---|---|---|---|---|---|
rpoB | 761143 | p.Lys446Thr | missense_variant | 0.18 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575412 | p.Glu22Ala | missense_variant | 0.33 |
mshA | 576775 | c.1428C>T | synonymous_variant | 0.2 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.17 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.17 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.19 |
mmpL5 | 779184 | c.-704C>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
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 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.24 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.51 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.55 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746628 | p.Asp324Val | missense_variant | 0.17 |
Rv2752c | 3064830 | c.1362C>G | synonymous_variant | 0.17 |
thyX | 3067510 | p.Leu146Met | missense_variant | 0.12 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.2 |
Rv3236c | 3612521 | p.Ser199Trp | missense_variant | 0.11 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.28 |
rpoA | 3878560 | c.-53C>T | upstream_gene_variant | 0.4 |
clpC1 | 4038442 | p.Ala755Thr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245553 | p.Pro774His | missense_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.4 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.4 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.6 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.6 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |