Run ID: ERR2229443
Sample name:
Date: 31-03-2023 17:11:44
Number of reads: 398488
Percentage reads mapped: 99.35
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326879 | c.594delC | frameshift_variant | 0.5 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491054 | p.Ala91Asp | missense_variant | 0.22 |
ccsA | 620375 | p.Pro162Leu | missense_variant | 0.29 |
rpoB | 762183 | p.Gly793Arg | missense_variant | 0.17 |
rpoC | 763378 | c.9C>T | synonymous_variant | 0.12 |
rpoC | 765053 | p.Ser562Pro | missense_variant | 0.29 |
rpoC | 765261 | p.Ala631Asp | missense_variant | 0.4 |
rpoC | 766234 | c.2867delG | frameshift_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775743 | p.Gly913Asp | missense_variant | 0.13 |
mmpL5 | 776285 | c.2196C>A | synonymous_variant | 0.12 |
mmpL5 | 776460 | p.Ala674Val | missense_variant | 0.13 |
mmpL5 | 778474 | p.Val3Met | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800669 | c.-140G>T | upstream_gene_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304693 | p.Ala588Glu | missense_variant | 0.22 |
embR | 1417115 | p.Asn78Ile | missense_variant | 0.2 |
atpE | 1461013 | c.-32C>T | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472246 | n.401G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475066 | n.1409C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475632 | n.1975C>T | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.38 |
fabG1 | 1673557 | p.His40Tyr | missense_variant | 0.67 |
fabG1 | 1673891 | p.Ala151Val | missense_variant | 0.12 |
inhA | 1673991 | c.-211C>T | upstream_gene_variant | 0.17 |
inhA | 1674554 | c.356delG | frameshift_variant | 0.5 |
rpsA | 1834005 | p.Met155Lys | missense_variant | 0.22 |
rpsA | 1834161 | p.Gln207Arg | missense_variant | 0.22 |
rpsA | 1834549 | p.Gln336His | missense_variant | 0.2 |
rpsA | 1834605 | p.Arg355Leu | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153943 | p.Asp723Glu | missense_variant | 0.2 |
katG | 2156234 | c.-123G>T | upstream_gene_variant | 0.14 |
katG | 2156342 | c.-231G>T | upstream_gene_variant | 0.25 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.2 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.18 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.18 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.19 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288936 | c.306G>T | synonymous_variant | 0.15 |
pncA | 2289033 | p.Pro70Gln | missense_variant | 0.2 |
pncA | 2290185 | c.-944G>T | upstream_gene_variant | 0.33 |
pepQ | 2859427 | p.Pro331His | missense_variant | 0.21 |
pepQ | 2859447 | c.972G>A | synonymous_variant | 0.2 |
Rv2752c | 3065138 | p.Ile352Phe | missense_variant | 0.18 |
ald | 3087377 | c.558C>A | synonymous_variant | 0.12 |
ald | 3087527 | c.712delG | frameshift_variant | 0.18 |
fprA | 3474237 | c.231C>A | synonymous_variant | 0.14 |
Rv3236c | 3612306 | p.Ala271Pro | missense_variant | 0.17 |
Rv3236c | 3612395 | p.Ala241Asp | missense_variant | 0.12 |
Rv3236c | 3612659 | p.Ser153Trp | missense_variant | 0.29 |
fbiA | 3640804 | p.Ala88Thr | missense_variant | 0.2 |
ddn | 3986943 | p.Gly34Trp | missense_variant | 0.22 |
panD | 4043989 | p.Ala98Asp | missense_variant | 0.22 |
panD | 4044075 | c.207T>C | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243229 | c.-4C>A | upstream_gene_variant | 0.13 |
embB | 4248916 | c.2403G>T | synonymous_variant | 0.22 |
embB | 4249611 | p.Asn1033Thr | missense_variant | 0.18 |
aftB | 4266999 | p.Cys613Phe | missense_variant | 0.13 |
aftB | 4268170 | p.Ala223Thr | missense_variant | 0.22 |
aftB | 4268602 | p.Leu79Met | missense_variant | 0.25 |
ethA | 4326856 | p.Gln206His | missense_variant | 0.29 |
ethA | 4326969 | p.Glu169* | stop_gained | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |