Run ID: SRR1172065
Sample name:
Date: 03-04-2023 02:55:12
Number of reads: 2872897
Percentage reads mapped: 95.93
Strain: lineage3
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6741 | p.Glu501Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Trp | missense_variant | 1.0 | rifampicin |
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 0.98 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.88 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2156093 | c.18dupA | frameshift_variant | 1.0 | isoniazid |
pncA | 2288790 | c.450_451dupCT | frameshift_variant | 1.0 | pyrazinamide |
ald | 3087252 | c.436_437dupGC | frameshift_variant | 0.12 | cycloserine |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326980 | p.Gln165Pro | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.99 |
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 | 575410 | c.65_68delAGGG | frameshift_variant | 0.28 |
mshA | 575700 | c.356dupG | frameshift_variant | 0.14 |
mshA | 575859 | p.Val171Glu | missense_variant | 0.11 |
mshA | 576161 | p.Gly272Arg | missense_variant | 0.23 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475626 | n.1969T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.12 |
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 | 2169320 | p.Leu431Phe | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726116 | c.-77T>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087334 | c.517dupG | frameshift_variant | 0.12 |
ald | 3087794 | c.976_977dupGA | frameshift_variant | 0.15 |
ald | 3087892 | c.1074_1077dupCCTG | frameshift_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ubiA | 4269718 | p.Ala39Glu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |