Run ID: ERR245821
Sample name:
Date: 31-03-2023 18:22:57
Number of reads: 2226666
Percentage reads mapped: 99.6
Strain: lineage4.3.4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4327054 | p.Tyr140* | stop_gained | 0.21 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7799 | c.498A>C | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9435 | p.Leu712Val | missense_variant | 0.21 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.22 |
rpoB | 762249 | p.Leu815Val | missense_variant | 0.19 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.2 |
rpoC | 762839 | c.-531G>A | upstream_gene_variant | 0.29 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.44 |
rpoC | 765234 | p.Ala622Gly | missense_variant | 0.15 |
rpoC | 766361 | p.Val998Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416445 | p.Tyr301* | stop_gained | 0.22 |
embR | 1417136 | p.Ser71Ile | missense_variant | 0.38 |
embR | 1417501 | c.-154A>C | upstream_gene_variant | 0.23 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473343 | n.1498G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.24 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.26 |
inhA | 1674334 | p.Arg45Gly | missense_variant | 0.18 |
rpsA | 1834631 | p.Gln364Lys | missense_variant | 0.32 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154036 | p.Ser692Arg | missense_variant | 0.26 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.2 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.75 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.29 |
ahpC | 2726756 | c.564C>G | synonymous_variant | 0.24 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.22 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.25 |
pepQ | 2859680 | p.Leu247Val | missense_variant | 0.15 |
pepQ | 2859832 | p.Ala196Gly | missense_variant | 0.31 |
pepQ | 2859974 | p.Ala149Pro | missense_variant | 0.25 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.75 |
thyA | 3073800 | c.672G>C | synonymous_variant | 0.24 |
thyA | 3073817 | p.Gln219Glu | missense_variant | 0.5 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449673 | p.Tyr390* | stop_gained | 0.26 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475280 | p.Val425Gly | missense_variant | 0.33 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.18 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.25 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
rpoA | 3877766 | p.Ala248Pro | missense_variant | 0.29 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.23 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.25 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.28 |
clpC1 | 4040233 | p.Arg158Ser | missense_variant | 0.4 |
panD | 4043938 | p.Ile115Thr | missense_variant | 1.0 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.46 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.37 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.27 |
embA | 4244460 | p.Val410Leu | missense_variant | 0.25 |
embB | 4245713 | c.-801G>C | upstream_gene_variant | 0.27 |
embB | 4248725 | p.Ser738Ala | missense_variant | 0.2 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.16 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.25 |
whiB6 | 4338493 | p.Thr10Lys | missense_variant | 0.36 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.98 |