Run ID: ERR4827429
Sample name:
Date: 01-04-2023 18:02:30
Number of reads: 1131429
Percentage reads mapped: 99.53
Strain: lineage4.8
Drug-resistance: MDR-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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 762300 | p.Lys832Glu | missense_variant | 1.0 |
rpoC | 766255 | c.2886G>T | synonymous_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406150 | c.1191G>A | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.98 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
fabG1 | 1673560 | p.Lys41Gln | missense_variant | 0.1 |
inhA | 1674135 | c.-67C>T | upstream_gene_variant | 1.0 |
inhA | 1674279 | c.78A>G | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101740 | p.Gln435* | stop_gained | 0.13 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.13 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.13 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168863 | c.1750C>T | synonymous_variant | 1.0 |
PPE35 | 2168981 | c.1632A>T | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860200 | c.219G>A | synonymous_variant | 0.12 |
Rv2752c | 3067190 | c.-999C>A | upstream_gene_variant | 1.0 |
fbiD | 3339691 | p.Pro192Thr | missense_variant | 0.15 |
clpC1 | 4040242 | p.Thr155Ser | missense_variant | 0.12 |
clpC1 | 4040250 | p.Glu152Gly | missense_variant | 0.12 |
embC | 4240596 | p.Leu245Arg | missense_variant | 0.11 |
embC | 4240599 | p.Val246Ala | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Arg | missense_variant | 0.1 |
embA | 4244391 | c.1159C>T | synonymous_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.17 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.33 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.38 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.38 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.4 |
embB | 4247395 | c.882C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408094 | p.Gly37Arg | missense_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |