Run ID: ERR2229038
Sample name:
Date: 31-03-2023 16:31:33
Number of reads: 485682
Percentage reads mapped: 99.47
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 | 491159 | p.Lys126Met | missense_variant | 0.11 |
mshA | 576351 | p.Asp335Gly | missense_variant | 0.17 |
ccsA | 620707 | p.Val273Met | missense_variant | 0.22 |
rpoB | 759861 | c.58delA | frameshift_variant | 0.12 |
rpoB | 760510 | c.707delG | frameshift_variant | 0.11 |
rpoB | 760865 | c.1059_1060insA | frameshift_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.35 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.35 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.35 |
mmpL5 | 777766 | p.Gly239Arg | missense_variant | 0.2 |
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 | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834710 | p.Tyr390Cys | missense_variant | 0.14 |
rpsA | 1834789 | c.1248T>A | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154262 | p.Leu617His | missense_variant | 0.17 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2167871 | c.2742G>T | synonymous_variant | 0.14 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.17 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.17 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518430 | p.Asp106Tyr | missense_variant | 0.12 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.13 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.13 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.13 |
folC | 2747473 | c.126C>A | synonymous_variant | 0.2 |
ribD | 2987045 | c.207C>T | synonymous_variant | 0.33 |
ribD | 2987239 | p.Thr134Ile | missense_variant | 0.17 |
Rv2752c | 3066326 | c.-135C>T | upstream_gene_variant | 0.33 |
Rv2752c | 3066328 | c.-137T>C | upstream_gene_variant | 0.33 |
thyA | 3073979 | p.Gln165Lys | missense_variant | 0.13 |
Rv3236c | 3612241 | c.876G>T | synonymous_variant | 0.11 |
Rv3236c | 3612671 | p.Pro149Gln | missense_variant | 0.22 |
ddn | 3987015 | p.Gln58* | stop_gained | 0.22 |
embC | 4239718 | c.-145T>C | upstream_gene_variant | 0.18 |
embC | 4239822 | c.-41_-39delCCGinsTCA | upstream_gene_variant | 0.27 |
embC | 4240569 | p.Leu236His | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242978 | p.Leu1039Pro | missense_variant | 0.2 |
embC | 4243100 | p.Val1080Leu | missense_variant | 0.12 |
embB | 4247055 | p.Leu181Gln | missense_variant | 0.29 |
aftB | 4267944 | p.Tyr298Phe | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |