Run ID: ERR245835
Sample name:
Date: 31-03-2023 18:23:49
Number of reads: 10746811
Percentage reads mapped: 99.74
Strain: lineage4.9.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4327054 | p.Tyr140* | stop_gained | 0.18 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8445 | p.Arg382Gly | missense_variant | 0.27 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.2 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.32 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417501 | c.-154A>C | upstream_gene_variant | 0.29 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.24 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.46 |
Rv1979c | 2223145 | p.Arg7Lys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 1.0 |
pncA | 2289448 | c.-207G>A | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.25 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.71 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.3 |
ahpC | 2726756 | c.564C>G | synonymous_variant | 0.24 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.24 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.22 |
Rv2752c | 3067191 | c.-1000G>A | upstream_gene_variant | 0.99 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.2 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
Rv3083 | 3449058 | p.Ser185Arg | missense_variant | 0.3 |
Rv3083 | 3449673 | p.Tyr390* | stop_gained | 0.24 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.3 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.22 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.21 |
clpC1 | 4039363 | p.Ala448Pro | missense_variant | 0.33 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.23 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.2 |
embC | 4241128 | c.1266G>C | synonymous_variant | 0.23 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.59 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.47 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.28 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.18 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.4 |
embB | 4249504 | p.Gln997His | missense_variant | 0.21 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.16 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.23 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |