Run ID: ERR2229759
Sample name:
Date: 31-03-2023 17:33:17
Number of reads: 1004711
Percentage reads mapped: 98.03
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 |
fgd1 | 491476 | p.Lys232Glu | missense_variant | 0.11 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.25 |
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 |
embR | 1417065 | p.Ala95Thr | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169191 | c.1422G>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726375 | c.183C>T | synonymous_variant | 0.1 |
folC | 2746564 | c.1035A>T | synonymous_variant | 0.15 |
folC | 2746568 | c.1030_1031insT | frameshift_variant | 0.14 |
thyX | 3067350 | p.Arg199Gln | missense_variant | 0.15 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3475049 | p.Ile348Asn | missense_variant | 0.1 |
whiB7 | 3568780 | c.-101A>G | upstream_gene_variant | 0.11 |
clpC1 | 4040249 | p.Glu152Gly | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243378 | p.Ser49Thr | missense_variant | 0.12 |
embA | 4244498 | c.1266A>G | synonymous_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.1 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.1 |
embB | 4249751 | c.3238T>C | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |