Run ID: ERR037543
Sample name:
Date: 31-03-2023 08:36:34
Number of reads: 13734020
Percentage reads mapped: 99.46
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 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.28 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475536 | n.1879C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.17 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.32 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.24 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.39 |
ribD | 2986778 | c.-61G>A | upstream_gene_variant | 1.0 |
thyX | 3067995 | c.-50A>C | upstream_gene_variant | 0.19 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.16 |
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 | 0.75 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.3 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.19 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.14 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.18 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.2 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.28 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.17 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.31 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.15 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.35 |
aftB | 4267149 | p.Glu563Gly | missense_variant | 1.0 |
aftB | 4267155 | p.Gln561Arg | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.19 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.31 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448498 | c.-5_*1408del | transcript_ablation | 1.0 |