Run ID: ERR4815803
Sample name:
Date: 01-04-2023 14:04:25
Number of reads: 1014295
Percentage reads mapped: 98.88
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 | 764567 | p.Lys400Glu | missense_variant | 0.18 |
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 | 0.98 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474239 | n.582G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475104 | n.1447T>C | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154044 | p.Thr690Pro | missense_variant | 0.12 |
katG | 2155789 | p.His108Pro | missense_variant | 0.22 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746968 | p.Gly211Arg | missense_variant | 0.14 |
fbiD | 3339363 | p.Asp82Glu | missense_variant | 0.2 |
Rv3083 | 3448387 | c.-117C>A | upstream_gene_variant | 0.12 |
Rv3236c | 3612251 | c.865delT | frameshift_variant | 0.15 |
fbiA | 3640904 | p.Ala121Val | missense_variant | 1.0 |
rpoA | 3878535 | c.-28G>T | upstream_gene_variant | 0.4 |
embC | 4241605 | c.1744delA | frameshift_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244083 | p.Ala284Asp | missense_variant | 0.18 |
embB | 4249647 | p.Arg1045Leu | missense_variant | 0.17 |
aftB | 4267501 | p.Pro446Ser | missense_variant | 0.17 |
ethA | 4328034 | c.-561C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |