Run ID: SRR6257097
Sample name:
Date: 04-04-2023 13:26:12
Number of reads: 1056761
Percentage reads mapped: 95.6
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761095 | p.Leu430Pro | missense_variant | 1.0 | rifampicin |
rpoB | 761110 | p.Asp435Gly | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472362 | n.517C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288990 | c.250_251delAG | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
eis | 2715369 | c.-37G>T | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247553 | p.Ser347Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766087 | c.2718C>A | synonymous_variant | 0.11 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475880 | n.2223C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475881 | n.2224T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475882 | n.2225C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475895 | n.2238C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475914 | n.2257C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475920 | n.2263G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475924 | n.2267A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475933 | n.2276C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475939 | n.2282G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475944 | n.2287G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475947 | n.2290G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476353 | n.2696G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169998 | c.615T>A | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243209 | c.-23_-22delCG | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338563 | c.-42G>T | upstream_gene_variant | 1.0 |
whiB6 | 4338593 | c.-73delT | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |