Run ID: SRR023449
Sample name:
Date: 02-04-2023 14:12:09
Number of reads: 6138149
Percentage reads mapped: 93.59
Strain: lineage2.2.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Tyr | missense_variant | 1.0 | rifampicin |
pncA | 2288713 | p.Thr177Pro | missense_variant | 0.23 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.36 |
fgd1 | 491324 | p.Val181Gly | missense_variant | 0.43 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.98 |
mshA | 576594 | p.Val416Gly | missense_variant | 0.23 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759827 | p.Ser7Arg | missense_variant | 0.2 |
rpoB | 759831 | p.Thr9Pro | missense_variant | 0.28 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766632 | p.Val1088Gly | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.99 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.99 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.21 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407084 | p.Val86Gly | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.99 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918060 | p.Lys41Gln | missense_variant | 0.15 |
tlyA | 1918181 | p.Val81Gly | missense_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155778 | p.Thr112Pro | missense_variant | 0.39 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168470 | p.Thr715Pro | missense_variant | 0.26 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.18 |
PPE35 | 2169974 | c.639T>G | synonymous_variant | 0.34 |
Rv1979c | 2221889 | p.Val426Ile | missense_variant | 0.98 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518300 | c.186T>G | synonymous_variant | 0.31 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.4 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.31 |
folC | 2746314 | p.Arg429Trp | missense_variant | 0.14 |
pepQ | 2859904 | p.Val172Gly | missense_variant | 0.38 |
pepQ | 2860253 | p.Thr56Pro | missense_variant | 0.3 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.25 |
fbiD | 3339304 | p.Thr63Pro | missense_variant | 0.33 |
fbiD | 3339626 | p.His170Pro | missense_variant | 0.38 |
fbiD | 3339652 | p.Thr179Ser | missense_variant | 0.2 |
fbiD | 3339660 | c.543C>A | synonymous_variant | 0.2 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.29 |
Rv3083 | 3449318 | p.Glu272Gly | missense_variant | 0.23 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.97 |
Rv3236c | 3612422 | p.Val232Gly | missense_variant | 0.28 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878059 | p.Val150Gly | missense_variant | 0.24 |
ddn | 3986994 | p.Thr51Pro | missense_variant | 0.21 |
clpC1 | 4039566 | p.Val380Gly | missense_variant | 0.36 |
embC | 4240646 | p.Phe262Val | missense_variant | 0.39 |
embC | 4242326 | p.Thr822Pro | missense_variant | 0.25 |
embC | 4242341 | p.Thr827Pro | missense_variant | 0.35 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.28 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244217 | p.Thr329Pro | missense_variant | 0.26 |
embA | 4244605 | p.Val458Gly | missense_variant | 0.38 |
embA | 4244668 | p.Val479Gly | missense_variant | 0.29 |
embA | 4244905 | p.Val558Gly | missense_variant | 0.45 |
embA | 4246085 | p.Glu951Asp | missense_variant | 0.99 |
embB | 4247822 | p.Thr437Pro | missense_variant | 0.47 |
embB | 4248663 | p.Val717Gly | missense_variant | 0.28 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326925 | p.Ser183Arg | missense_variant | 0.41 |
whiB6 | 4338536 | c.-15G>T | upstream_gene_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |