Run ID: SRR6650139
Sample name:
Date: 04-04-2023 15:17:12
Number of reads: 1127803
Percentage reads mapped: 99.58
Strain: lineage4.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4327337 | c.136delG | frameshift_variant | 0.15 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6639 | p.Ala467Glu | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8599 | p.Gln433Leu | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491589 | c.807G>A | synonymous_variant | 0.17 |
rpoC | 762896 | c.-474G>A | upstream_gene_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765991 | c.2622C>A | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472421 | n.576G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473774 | n.117G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475196 | n.1540delG | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475527 | n.1870A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476422 | n.2765C>T | non_coding_transcript_exon_variant | 0.18 |
inhA | 1673368 | c.-834A>G | upstream_gene_variant | 1.0 |
fabG1 | 1673789 | p.Phe117Ser | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 0.13 |
PPE35 | 2169510 | p.Asn368Thr | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
folC | 2746926 | c.672delC | frameshift_variant | 0.12 |
pepQ | 2860150 | p.Ala90Val | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339155 | p.Ile13Asn | missense_variant | 0.1 |
Rv3083 | 3448398 | c.-106G>T | upstream_gene_variant | 1.0 |
Rv3083 | 3448877 | p.Thr125Ile | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474158 | p.Ser51Tyr | missense_variant | 0.11 |
fprA | 3474342 | p.Leu112Phe | missense_variant | 0.11 |
Rv3236c | 3612265 | c.852G>C | synonymous_variant | 0.12 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 0.96 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244969 | c.1737G>A | synonymous_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ethA | 4326084 | p.Asp464Asn | missense_variant | 0.11 |
ethA | 4326678 | p.Ser266Gly | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |