Run ID: ERR2229671
Sample name:
Date: 31-03-2023 17:24:20
Number of reads: 749834
Percentage reads mapped: 99.43
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 | 6201 | p.Arg321Pro | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
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 | 0.95 |
rrl | 1474655 | n.998T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474670 | n.1013C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475080 | n.1426delC | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1674092 | p.Ala218Asp | missense_variant | 0.12 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.13 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.14 |
Rv1979c | 2221838 | p.Gly443Ser | missense_variant | 0.2 |
Rv1979c | 2221884 | c.1281G>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726441 | c.249G>A | synonymous_variant | 0.12 |
Rv2752c | 3065780 | p.Val138Met | missense_variant | 0.11 |
Rv3236c | 3612759 | p.Gly120Ser | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245523 | c.2294delG | frameshift_variant | 0.13 |
embB | 4245737 | c.-777A>G | upstream_gene_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.13 |
ethA | 4326115 | c.1359A>T | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |