Run ID: ERR4820537
Sample name:
Date: 01-04-2023 16:44:25
Number of reads: 2942392
Percentage reads mapped: 94.35
Strain: lineage1.2.2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 1.0 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8668 | p.Ala456Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_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 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472263 | n.418C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472279 | n.434T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472514 | n.669T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472712 | n.867G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476128 | n.2471T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476422 | n.2765C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476638 | n.2981C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476706 | n.3049C>T | non_coding_transcript_exon_variant | 0.17 |
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 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222398 | p.Ile256Thr | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878656 | c.-149C>A | upstream_gene_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268323 | p.Leu172Phe | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407742 | p.Arg154Pro | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |