Run ID: SRR3732654
Sample name:
Date: 04-04-2023 05:37:11
Number of reads: 486667
Percentage reads mapped: 99.3
Strain: lineage4
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761108 | p.Met434Ile | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5161 | c.-79C>A | upstream_gene_variant | 0.33 |
gyrB | 6347 | p.Gln370Lys | missense_variant | 0.4 |
gyrB | 7079 | p.Gly614Cys | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7380 | p.Ser27Cys | missense_variant | 0.4 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
fgd1 | 491182 | p.Glu134* | stop_gained | 0.29 |
fgd1 | 491385 | p.Glu201Asp | missense_variant | 0.4 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 0.33 |
rpoC | 762770 | c.-600C>A | upstream_gene_variant | 0.67 |
rpoC | 762965 | c.-405T>C | upstream_gene_variant | 0.25 |
rpoC | 763676 | p.His103Asn | missense_variant | 0.22 |
rpoC | 763733 | p.Pro122Thr | missense_variant | 0.4 |
rpoC | 764258 | p.Lys297Glu | missense_variant | 0.5 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.67 |
rpoC | 764543 | p.Thr392Asp | missense_variant | 0.67 |
rpoC | 765628 | c.2259G>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781403 | c.-157G>T | upstream_gene_variant | 0.29 |
rpsL | 781709 | c.150G>T | synonymous_variant | 0.25 |
embR | 1416758 | p.Leu197Pro | missense_variant | 0.33 |
embR | 1417248 | c.99delC | frameshift_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471779 | n.-67T>A | upstream_gene_variant | 0.29 |
rrs | 1472102 | n.257G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476394 | n.2737C>A | non_coding_transcript_exon_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102695 | c.348C>A | synonymous_variant | 0.67 |
PPE35 | 2167968 | p.Pro882Gln | missense_variant | 0.4 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517996 | c.-119T>C | upstream_gene_variant | 0.5 |
ahpC | 2726285 | c.93C>T | synonymous_variant | 0.67 |
folC | 2747028 | p.Val191Ile | missense_variant | 0.22 |
pepQ | 2859749 | p.Ala224Thr | missense_variant | 0.5 |
thyA | 3073704 | c.768G>A | synonymous_variant | 1.0 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3475155 | c.1149C>A | synonymous_variant | 0.5 |
fprA | 3475237 | p.Ala411Thr | missense_variant | 0.25 |
fprA | 3475251 | c.1245G>T | synonymous_variant | 0.25 |
fprA | 3475300 | p.Ala432Leu | missense_variant | 0.25 |
whiB7 | 3568467 | p.Phe71Leu | missense_variant | 0.33 |
Rv3236c | 3612511 | p.Trp202Cys | missense_variant | 0.5 |
fbiA | 3640670 | p.Ala43Asp | missense_variant | 0.33 |
alr | 3841419 | p.Val1Glu | missense_variant | 0.29 |
rpoA | 3878384 | p.Leu42Met | missense_variant | 0.4 |
ddn | 3987011 | c.168C>T | synonymous_variant | 1.0 |
clpC1 | 4038668 | c.2037G>T | synonymous_variant | 0.33 |
clpC1 | 4039783 | p.Leu308Met | missense_variant | 0.25 |
clpC1 | 4040553 | p.Ser51* | stop_gained | 0.14 |
panD | 4043879 | c.403C>A | synonymous_variant | 0.67 |
panD | 4044107 | p.Ala59Thr | missense_variant | 0.29 |
embC | 4239881 | p.Pro7Thr | missense_variant | 0.5 |
embC | 4240776 | p.Glu305Gly | missense_variant | 0.29 |
embC | 4241866 | c.2004G>T | synonymous_variant | 0.5 |
embC | 4241921 | p.Gly687Trp | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244531 | c.1299G>T | synonymous_variant | 0.4 |
embB | 4248028 | c.1515C>A | synonymous_variant | 0.67 |
embB | 4248432 | p.Trp640Leu | missense_variant | 0.67 |
embB | 4248799 | c.2286T>C | synonymous_variant | 0.25 |
embB | 4249086 | p.Leu858Pro | missense_variant | 0.67 |
embB | 4249633 | c.3120C>A | synonymous_variant | 0.33 |
ethA | 4326208 | c.1266G>T | synonymous_variant | 1.0 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4326999 | p.Gly159Trp | missense_variant | 0.25 |
ethR | 4327444 | c.-105C>A | upstream_gene_variant | 0.33 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |