Run ID: ERR2513306
Sample name:
Date: 31-03-2023 19:35:31
Number of reads: 779221
Percentage reads mapped: 99.65
Strain: lineage4.1.2.1
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 | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.99 |
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 |
gyrA | 9384 | p.Arg695Gly | missense_variant | 0.11 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575267 | c.-81G>A | upstream_gene_variant | 0.12 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575842 | c.495G>A | synonymous_variant | 0.13 |
ccsA | 620157 | c.267G>C | synonymous_variant | 0.1 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762225 | p.Glu807Gln | missense_variant | 0.13 |
rpoB | 762373 | p.Pro856Gln | missense_variant | 0.14 |
rpoC | 762518 | c.-852C>T | upstream_gene_variant | 0.13 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765782 | p.Ser805Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776045 | c.2436G>A | synonymous_variant | 0.13 |
mmpS5 | 778842 | p.Gly22Ser | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303133 | p.Ala68Val | missense_variant | 0.12 |
fbiC | 1305373 | p.Thr815Ala | missense_variant | 0.12 |
Rv1258c | 1407143 | c.198C>T | synonymous_variant | 0.22 |
Rv1258c | 1407410 | c.-70C>A | upstream_gene_variant | 0.12 |
Rv1258c | 1407509 | c.-169C>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471781 | n.-65G>A | upstream_gene_variant | 1.0 |
rrl | 1475602 | n.1945G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674435 | c.234G>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156368 | c.-257G>T | upstream_gene_variant | 0.11 |
PPE35 | 2168160 | p.Glu818Val | missense_variant | 0.11 |
PPE35 | 2168296 | p.Glu773* | stop_gained | 0.12 |
PPE35 | 2169570 | p.Ser348Asn | missense_variant | 0.12 |
PPE35 | 2169573 | p.Phe347Tyr | missense_variant | 0.12 |
PPE35 | 2169578 | c.1035T>C | synonymous_variant | 0.14 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.17 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.13 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.12 |
PPE35 | 2170363 | p.Glu84Lys | missense_variant | 0.2 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.2 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.12 |
pncA | 2290057 | c.-816G>T | upstream_gene_variant | 0.15 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518234 | p.Glu40Asp | missense_variant | 0.2 |
kasA | 2519356 | c.1242G>A | synonymous_variant | 0.12 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.24 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.18 |
folC | 2746866 | p.Leu245Met | missense_variant | 0.14 |
pepQ | 2859756 | p.Asp221Glu | missense_variant | 0.11 |
pepQ | 2859976 | c.441_442delCG | frameshift_variant | 0.14 |
pepQ | 2860042 | p.Gly126Glu | missense_variant | 0.13 |
Rv2752c | 3064917 | c.1275C>T | synonymous_variant | 0.11 |
Rv2752c | 3067117 | c.-926C>G | upstream_gene_variant | 0.12 |
thyX | 3067481 | c.465C>A | synonymous_variant | 0.17 |
thyA | 3073713 | c.759G>A | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087160 | p.Ser114* | stop_gained | 0.11 |
Rv3083 | 3448667 | p.Ser55Leu | missense_variant | 0.2 |
Rv3083 | 3448787 | p.Asp95Val | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474078 | c.72G>A | synonymous_variant | 0.2 |
fprA | 3474137 | p.Thr44Asn | missense_variant | 0.12 |
fprA | 3474144 | p.Trp46Cys | missense_variant | 0.11 |
Rv3236c | 3612845 | p.Pro91Leu | missense_variant | 0.12 |
Rv3236c | 3612910 | p.Leu69Phe | missense_variant | 0.15 |
alr | 3840919 | p.Gly168* | stop_gained | 0.13 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.14 |
ddn | 3986703 | c.-141T>C | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243488 | p.Gly86Cys | missense_variant | 0.12 |
embA | 4244048 | c.816C>T | synonymous_variant | 0.12 |
embA | 4245441 | p.Asp737Asn | missense_variant | 0.17 |
embB | 4246675 | c.162G>T | synonymous_variant | 0.22 |
aftB | 4267159 | p.Thr560Ser | missense_variant | 0.11 |
ethA | 4326483 | p.Arg331Cys | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |