Run ID: ERR4819751
Sample name:
Date: 01-04-2023 16:17:08
Number of reads: 600603
Percentage reads mapped: 99.7
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776113 | p.Ile790Val | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304947 | p.Asp673Asn | missense_variant | 0.12 |
fbiC | 1305363 | c.2433G>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2221940 | p.Arg409* | stop_gained | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726012 | c.-181T>C | upstream_gene_variant | 0.15 |
pepQ | 2860325 | p.Tyr32His | missense_variant | 1.0 |
Rv2752c | 3064603 | p.Ala530Val | missense_variant | 0.2 |
Rv2752c | 3065524 | p.His223Arg | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087878 | p.Glu353Asp | missense_variant | 0.2 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.12 |
clpC1 | 4040340 | p.Gln122Pro | missense_variant | 0.29 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.11 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244989 | p.Ala586Val | missense_variant | 0.14 |
embB | 4248520 | p.Ser669Arg | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |