Run ID: ERR2228970
Sample name:
Date: 31-03-2023 16:28:47
Number of reads: 441100
Percentage reads mapped: 99.59
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 | 761116 | p.Asn437Ile | missense_variant | 0.12 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5714 | p.Lys159* | stop_gained | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575505 | p.His53Leu | missense_variant | 0.15 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
ccsA | 620366 | p.Asn159Ser | missense_variant | 0.13 |
ccsA | 620469 | p.Ser193Arg | missense_variant | 0.15 |
rpoB | 762456 | p.Gly884Arg | missense_variant | 0.15 |
rpoB | 763252 | c.3448delG | frameshift_variant | 0.25 |
rpoC | 763478 | p.Arg37Ser | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775852 | p.Ser877Gly | missense_variant | 0.13 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.25 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.25 |
mmpL5 | 777732 | c.748dupC | frameshift_variant | 0.14 |
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 |
rrs | 1473325 | n.1480G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.22 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.2 |
PPE35 | 2168238 | p.Pro792Gln | missense_variant | 0.5 |
PPE35 | 2168477 | c.2136C>A | synonymous_variant | 0.11 |
PPE35 | 2168500 | p.Ser705Pro | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169935 | c.678C>T | synonymous_variant | 0.25 |
Rv1979c | 2221862 | p.Arg435Cys | missense_variant | 0.15 |
Rv1979c | 2222842 | p.Val108Glu | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726371 | p.Val60Ala | missense_variant | 0.2 |
ribD | 2986698 | c.-141G>A | upstream_gene_variant | 0.18 |
ribD | 2986743 | c.-96G>T | upstream_gene_variant | 0.17 |
ribD | 2987263 | p.Val142Glu | missense_variant | 0.12 |
ribD | 2987454 | p.Asp206Asn | missense_variant | 0.14 |
thyA | 3074271 | c.201C>G | synonymous_variant | 0.29 |
ald | 3087150 | p.Gly111Ser | missense_variant | 0.18 |
Rv3236c | 3612631 | p.Met162Ile | missense_variant | 0.2 |
alr | 3840856 | p.Arg189Gly | missense_variant | 0.14 |
rpoA | 3877678 | p.Ala277Glu | missense_variant | 0.2 |
clpC1 | 4038843 | p.Val621Glu | missense_variant | 0.14 |
clpC1 | 4040291 | c.414G>A | synonymous_variant | 0.18 |
embC | 4240683 | p.Asp274Val | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245456 | p.Glu742Gln | missense_variant | 0.14 |
embB | 4248783 | p.Pro757His | missense_variant | 0.15 |
ethA | 4326699 | p.Arg259Cys | missense_variant | 0.11 |
ethA | 4327713 | c.-240A>C | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408431 | c.-229G>A | upstream_gene_variant | 0.33 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |