Run ID: SRR11972247
Sample name:
Date: 03-04-2023 05:33:23
Number of reads: 161600
Percentage reads mapped: 99.46
Strain:
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 0.93 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247574 | p.Asp354Ala | missense_variant | 0.58 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 0.22 |
gyrB | 5172 | c.-68C>T | upstream_gene_variant | 0.14 |
gyrB | 5653 | c.414G>A | synonymous_variant | 0.33 |
gyrB | 5673 | p.Glu145Val | missense_variant | 0.2 |
gyrB | 5836 | c.597C>T | synonymous_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7935 | p.Glu212* | stop_gained | 0.13 |
gyrA | 8039 | c.740delG | frameshift_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491124 | c.342C>T | synonymous_variant | 0.67 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759664 | c.-143G>A | upstream_gene_variant | 0.22 |
rpoB | 760519 | p.Thr238Ile | missense_variant | 0.4 |
rpoB | 760917 | p.Arg371Gly | missense_variant | 0.5 |
rpoB | 762311 | c.2505C>T | synonymous_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763151 | c.-219C>T | upstream_gene_variant | 0.33 |
rpoC | 764695 | c.1326T>A | synonymous_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777757 | p.Ala242Thr | missense_variant | 0.25 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801361 | p.Val185Leu | missense_variant | 0.22 |
fbiC | 1303836 | c.906G>A | synonymous_variant | 0.5 |
fbiC | 1304894 | p.Gly655Asp | missense_variant | 1.0 |
fbiC | 1305449 | p.Ile840Thr | missense_variant | 0.18 |
Rv1258c | 1406484 | p.Pro286His | missense_variant | 0.29 |
embR | 1417368 | c.-21G>A | upstream_gene_variant | 0.18 |
embR | 1417390 | c.-43A>T | upstream_gene_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471856 | n.11A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473216 | n.1371C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473228 | n.1383T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473514 | n.-144C>T | upstream_gene_variant | 0.17 |
rrl | 1473658 | n.1T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474553 | n.896T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1674044 | p.Ala202Glu | missense_variant | 0.15 |
inhA | 1674415 | p.Ala72Thr | missense_variant | 0.4 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>A | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102975 | p.Gly23Glu | missense_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.5 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.5 |
PPE35 | 2170198 | p.Ala139Thr | missense_variant | 0.25 |
Rv1979c | 2222838 | c.327G>A | synonymous_variant | 0.29 |
Rv1979c | 2222902 | p.Arg88His | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289345 | c.-104G>A | upstream_gene_variant | 0.5 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
ribD | 2986971 | p.Phe45Ile | missense_variant | 0.4 |
ribD | 2987021 | c.183G>A | synonymous_variant | 0.4 |
thyA | 3073857 | c.615C>T | synonymous_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841510 | c.-90A>G | upstream_gene_variant | 0.25 |
alr | 3841539 | c.-119C>T | upstream_gene_variant | 0.2 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.43 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.17 |
ddn | 3986944 | p.Gly34Val | missense_variant | 0.25 |
clpC1 | 4040166 | p.Ala180Val | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243269 | p.Ala13Thr | missense_variant | 0.18 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243505 | c.273C>G | synonymous_variant | 0.22 |
embA | 4245116 | c.1884C>T | synonymous_variant | 0.17 |
embA | 4246143 | p.Ile971Phe | missense_variant | 0.29 |
embB | 4247137 | c.624C>A | synonymous_variant | 0.2 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4249455 | p.Thr981Met | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268267 | c.570G>T | synonymous_variant | 0.17 |
aftB | 4268487 | p.Met117Thr | missense_variant | 0.17 |
whiB6 | 4338379 | p.Glu48Gly | missense_variant | 0.22 |
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 |