Run ID: ERR2229022
Sample name:
Date: 31-03-2023 16:30:42
Number of reads: 745658
Percentage reads mapped: 99.63
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 |
---|---|---|---|---|
gyrB | 6753 | p.Ile505Thr | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 761655 | c.1853delC | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776988 | p.Pro498Gln | missense_variant | 0.12 |
mmpL5 | 777146 | c.1335C>A | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781603 | p.Lys15Arg | missense_variant | 0.11 |
fbiC | 1303243 | p.Cys105Arg | missense_variant | 0.11 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407165 | p.Thr59Met | missense_variant | 0.12 |
atpE | 1461052 | p.Pro3His | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673990 | p.Gly184Asp | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169053 | c.1560T>A | synonymous_variant | 0.2 |
PPE35 | 2169091 | p.Val508Leu | missense_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.1 |
PPE35 | 2170513 | c.100C>T | synonymous_variant | 0.12 |
PPE35 | 2170528 | p.Ser29Thr | missense_variant | 0.12 |
PPE35 | 2170532 | c.81G>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519281 | c.1167G>A | synonymous_variant | 0.11 |
eis | 2714853 | c.480C>A | synonymous_variant | 0.18 |
pepQ | 2859622 | p.Pro266Leu | missense_variant | 0.17 |
Rv3083 | 3448447 | c.-56delA | upstream_gene_variant | 0.17 |
fbiB | 3642601 | p.Gly356Glu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244611 | p.Ala460Val | missense_variant | 0.13 |
embB | 4246082 | c.-432T>C | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |