Run ID: ERR4796257
Sample name:
Date: 01-04-2023 06:46:36
Number of reads: 2587295
Percentage reads mapped: 92.17
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 | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289162 | p.Leu27Pro | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | 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 | 576108 | p.Ala254Gly | missense_variant | 0.29 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766488 | p.Pro1040Arg | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | 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 | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474551 | n.894G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474557 | n.900G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474649 | n.992A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474652 | n.996delA | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474658 | n.1001A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474673 | n.1016T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475080 | n.1423G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475082 | n.1425C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475137 | n.1480A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.15 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726142 | c.-51G>A | upstream_gene_variant | 1.0 |
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 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
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 |