Run ID: ERR4817460
Sample name:
Date: 01-04-2023 15:00:17
Number of reads: 466009
Percentage reads mapped: 99.65
Strain: lineage4.1.2
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7179 | p.Leu647Ser | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761061 | p.Ala419Thr | missense_variant | 0.2 |
rpoB | 761341 | p.Lys512Arg | missense_variant | 0.14 |
rpoB | 762653 | p.Trp949Cys | missense_variant | 0.13 |
rpoB | 762847 | p.Pro1014Arg | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778928 | c.-448T>C | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801380 | p.Val191Glu | missense_variant | 0.18 |
fbiC | 1305135 | c.2205C>A | synonymous_variant | 0.1 |
embR | 1417140 | p.Ala70Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 1.0 |
tlyA | 1917785 | c.-155C>T | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155525 | p.Val196Asp | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289945 | c.-704T>A | upstream_gene_variant | 0.22 |
folC | 2747022 | p.Val193Ile | missense_variant | 1.0 |
folC | 2747025 | p.Ala192Thr | missense_variant | 0.22 |
pepQ | 2859501 | c.918G>A | synonymous_variant | 0.17 |
pepQ | 2859769 | p.Phe217Ser | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339512 | p.Ala132Glu | missense_variant | 0.11 |
Rv3083 | 3448821 | c.318C>T | synonymous_variant | 0.67 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 1.0 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474676 | p.Val224Met | missense_variant | 0.14 |
fprA | 3475279 | p.Val425Met | missense_variant | 0.25 |
whiB7 | 3568648 | p.Pro11His | missense_variant | 0.2 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 1.0 |
fbiB | 3642335 | p.Ser267Arg | missense_variant | 0.12 |
alr | 3840894 | p.Leu176Pro | missense_variant | 0.15 |
rpoA | 3877774 | p.Ala245Glu | missense_variant | 0.11 |
rpoA | 3878393 | p.Arg39Ser | missense_variant | 0.18 |
rpoA | 3878429 | p.Glu27* | stop_gained | 0.17 |
ddn | 3986821 | c.-23C>T | upstream_gene_variant | 0.12 |
clpC1 | 4039328 | c.1377A>T | synonymous_variant | 0.22 |
embC | 4241656 | c.1794G>T | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244239 | p.Trp336Ser | missense_variant | 0.22 |
aftB | 4268649 | p.Trp63* | stop_gained | 0.22 |
ubiA | 4268996 | p.Arg280Cys | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |