Run ID: ERR028317
Sample name:
Date: 31-03-2023 08:21:49
Number of reads: 800403
Percentage reads mapped: 99.15
Strain: lineage6;lineage5.1;lineage4.2.2;lineage1.1.3.1;lineage1.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.42 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.33 |
lineage5 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.07 |
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 0.05 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.25 |
lineage5.1 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.06 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.06 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 0.09 |
lineage1.1.1 | Indo-Oceanic | EAI4;EAI5 | RD239 | 0.13 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.06 |
lineage1.1.3.1 | Indo-Oceanic | NA | RD239 | 0.06 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5081 | c.-159G>C | upstream_gene_variant | 0.21 |
gyrB | 5698 | c.459G>A | synonymous_variant | 0.18 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.33 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 0.3 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7538 | p.Glu79Asp | missense_variant | 0.12 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.38 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.52 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9629 | c.2328C>T | synonymous_variant | 0.12 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.12 |
fgd1 | 491668 | p.Lys296Glu | missense_variant | 0.1 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.5 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.2 |
rpoB | 759831 | p.Thr9Pro | missense_variant | 0.48 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.61 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.43 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.43 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775753 | c.2727delC | frameshift_variant | 0.3 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.62 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 0.33 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.44 |
atpE | 1461083 | c.39T>G | synonymous_variant | 0.24 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474709 | n.1052G>T | non_coding_transcript_exon_variant | 0.2 |
inhA | 1673338 | c.-864G>A | upstream_gene_variant | 0.14 |
rpsA | 1834299 | p.Gln253Arg | missense_variant | 0.13 |
rpsA | 1834319 | p.Val260Ile | missense_variant | 0.12 |
rpsA | 1834631 | p.Gln364Lys | missense_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.15 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.79 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.46 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.32 |
PPE35 | 2169379 | p.Phe412Val | missense_variant | 0.33 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.29 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.64 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289622 | c.-381C>T | upstream_gene_variant | 0.19 |
pncA | 2290062 | c.-821G>A | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.7 |
kasA | 2518675 | p.Met187Ile | missense_variant | 0.15 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.29 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.24 |
pepQ | 2860436 | c.-18C>T | upstream_gene_variant | 0.12 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.28 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 0.3 |
thyX | 3067976 | c.-31T>G | upstream_gene_variant | 0.29 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.5 |
thyA | 3074654 | c.-183T>G | upstream_gene_variant | 0.18 |
ald | 3086705 | c.-115T>G | upstream_gene_variant | 0.17 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.5 |
ald | 3087084 | c.266delA | frameshift_variant | 0.27 |
fbiD | 3339153 | p.Leu12Phe | missense_variant | 0.19 |
fbiD | 3339335 | p.Ala73Gly | missense_variant | 0.25 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.43 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474256 | p.Val84Phe | missense_variant | 0.12 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.43 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.58 |
Rv3236c | 3612422 | p.Val232Gly | missense_variant | 0.43 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.17 |
alr | 3840932 | c.489C>T | synonymous_variant | 0.21 |
alr | 3841498 | c.-78A>G | upstream_gene_variant | 0.17 |
rpoA | 3877696 | p.Thr271Ile | missense_variant | 0.24 |
rpoA | 3878238 | p.Asp90Glu | missense_variant | 0.2 |
ddn | 3986987 | c.144G>T | synonymous_variant | 0.4 |
ddn | 3987180 | p.Asp113Asn | missense_variant | 0.14 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.25 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.33 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.47 |
clpC1 | 4040824 | c.-120C>T | upstream_gene_variant | 0.38 |
embC | 4239843 | c.-20A>C | upstream_gene_variant | 0.25 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.33 |
embC | 4241011 | c.1149C>T | synonymous_variant | 0.13 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.22 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 0.33 |
embA | 4244096 | c.864C>T | synonymous_variant | 0.31 |
embA | 4245147 | p.Pro639Ser | missense_variant | 0.2 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.43 |
embB | 4246164 | c.-350T>C | upstream_gene_variant | 0.19 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.5 |
embB | 4248725 | p.Ser738Ala | missense_variant | 0.27 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.67 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.75 |
ethR | 4326928 | c.-621G>A | upstream_gene_variant | 0.12 |
ethA | 4327103 | p.Gly124Asp | missense_variant | 0.17 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 0.1 |
whiB6 | 4338242 | p.Gln94Glu | missense_variant | 0.33 |
whiB6 | 4338546 | c.-25G>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.4 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.62 |
gid | 4407780 | c.423G>A | synonymous_variant | 0.12 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.46 |