Run ID: ERR4831840
Sample name:
Date: 01-04-2023 21:09:19
Number of reads: 1918594
Percentage reads mapped: 98.29
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Asn | missense_variant | 0.96 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.97 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 0.97 | 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 | 0.96 |
rpoC | 764923 | p.Glu518Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.95 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776510 | c.1971C>A | synonymous_variant | 0.11 |
mmpL5 | 776869 | c.1612C>A | synonymous_variant | 0.11 |
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 | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474613 | n.956T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475234 | n.1577C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.89 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156055 | c.57C>A | synonymous_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289082 | p.Pro54Ser | missense_variant | 0.94 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.23 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.23 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 0.96 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.98 |