Run ID: ERR245791
Sample name:
Date: 31-03-2023 18:21:33
Number of reads: 11130361
Percentage reads mapped: 99.29
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7323 | p.Pro8Ala | missense_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7493 | c.192C>T | synonymous_variant | 0.19 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8445 | p.Arg382Gly | missense_variant | 0.46 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 759831 | p.Thr9Pro | missense_variant | 0.24 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.33 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 767305 | p.Tyr1312* | stop_gained | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776659 | p.Asp608Asn | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.16 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417501 | c.-154A>C | upstream_gene_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.16 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.39 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918069 | p.Thr44Pro | missense_variant | 0.47 |
PPE35 | 2168501 | p.Phe704Leu | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.15 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.41 |
PPE35 | 2170156 | p.Ala153Pro | missense_variant | 0.48 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.27 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.67 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.22 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449058 | p.Ser185Arg | missense_variant | 0.32 |
Rv3083 | 3449673 | p.Tyr390* | stop_gained | 0.27 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.18 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.25 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.25 |
clpC1 | 4039363 | p.Ala448Pro | missense_variant | 0.33 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.34 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.53 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.48 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.23 |
embB | 4247121 | p.Ser203Leu | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.16 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |