Run ID: ERR046781
Sample name:
Date: 31-03-2023 08:51:05
Number of reads: 9318054
Percentage reads mapped: 99.47
Strain: lineage4.4.1.2
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 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.2 | Euro-American | T1 | 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 |
mshA | 575309 | c.-39C>G | upstream_gene_variant | 0.17 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.27 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.3 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.21 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.21 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 0.99 |
PPE35 | 2167871 | c.2742G>C | synonymous_variant | 0.19 |
PPE35 | 2169379 | p.Phe412Val | missense_variant | 0.2 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.26 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.16 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.46 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.17 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.21 |
pepQ | 2860213 | p.Pro69Leu | missense_variant | 1.0 |
Rv2752c | 3064552 | p.Arg547Pro | missense_variant | 0.21 |
Rv2752c | 3064594 | p.Val533Ala | missense_variant | 1.0 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.37 |
thyX | 3067995 | c.-50A>C | upstream_gene_variant | 0.24 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475280 | p.Val425Gly | missense_variant | 0.24 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.17 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.17 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.19 |
clpC1 | 4039363 | p.Ala448Pro | missense_variant | 0.28 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.25 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.38 |
embC | 4241873 | c.2011C>T | synonymous_variant | 1.0 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.3 |
embA | 4245250 | p.His673Arg | missense_variant | 0.99 |
embB | 4248769 | c.2256C>T | synonymous_variant | 1.0 |
embB | 4249012 | c.2499G>A | synonymous_variant | 0.99 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.23 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |