Run ID: ERR4820451
Sample name:
Date: 01-04-2023 16:41:24
Number of reads: 651532
Percentage reads mapped: 99.66
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 | 490720 | c.-63T>A | upstream_gene_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778150 | p.Gln111Lys | missense_variant | 0.11 |
mmpR5 | 779403 | p.Glu138Asp | missense_variant | 0.12 |
mmpS5 | 779661 | c.-756C>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800720 | c.-89T>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673162 | c.-278T>C | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169911 | c.702C>T | synonymous_variant | 1.0 |
Rv1979c | 2222351 | p.Thr272Ala | missense_variant | 0.17 |
Rv1979c | 2223242 | c.-78A>G | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518048 | c.-67C>T | upstream_gene_variant | 0.18 |
ribD | 2987007 | p.Gly57Cys | missense_variant | 0.22 |
Rv2752c | 3065061 | p.Tyr377* | stop_gained | 0.13 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.18 |
Rv3236c | 3612047 | p.Ala357Val | missense_variant | 1.0 |
fbiA | 3640630 | p.Ala30Thr | missense_variant | 1.0 |
alr | 3841570 | c.-150T>C | upstream_gene_variant | 0.11 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.22 |
rpoA | 3878171 | c.336delG | frameshift_variant | 0.18 |
ddn | 3986727 | c.-117A>G | upstream_gene_variant | 0.12 |
ddn | 3986922 | p.Trp27Arg | missense_variant | 0.11 |
clpC1 | 4039245 | p.Val487Ala | missense_variant | 0.11 |
clpC1 | 4039307 | c.1397delA | frameshift_variant | 0.18 |
clpC1 | 4039939 | p.Val256Met | missense_variant | 0.12 |
panD | 4044034 | c.247delG | frameshift_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247129 | p.Ile206Val | missense_variant | 0.12 |
embB | 4247854 | c.1341C>T | synonymous_variant | 0.17 |
embB | 4248021 | c.1510delG | frameshift_variant | 0.14 |
embB | 4249209 | p.Val899Ala | missense_variant | 0.1 |
ubiA | 4269448 | p.Val129Asp | missense_variant | 0.14 |
ethA | 4326505 | c.969C>G | synonymous_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 |