Run ID: ERR2446091
Sample name:
Date: 15-08-2022 11:02:47
Number of reads: 357173
Percentage reads mapped: 99.98
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6113 | p.Gln292Lys | missense_variant | 0.14 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 6454 | c.-848C>A | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9096 | p.Leu599Met | missense_variant | 0.2 |
gyrA | 9592 | p.Gly764Val | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 762945 | p.Thr1047Ser | missense_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765930 | p.His854Leu | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775644 | p.Arg946Leu | missense_variant | 0.14 |
mmpL5 | 775697 | c.2784G>A | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472595 | n.750A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473055 | n.1210C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475058 | n.1401C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476389 | n.2732G>T | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834493 | p.Glu318* | stop_gained | 0.23 |
ndh | 2102587 | p.Leu152Phe | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169201 | p.Ser471* | stop_gained | 0.2 |
PPE35 | 2170628 | c.-16C>A | upstream_gene_variant | 0.2 |
PPE35 | 2170669 | c.-57G>T | upstream_gene_variant | 0.2 |
Rv1979c | 2221746 | c.1419G>T | synonymous_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289137 | c.105G>A | synonymous_variant | 1.0 |
ribD | 2986910 | c.72C>A | synonymous_variant | 0.15 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449229 | c.726T>C | synonymous_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.89 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475039 | p.Gly345Cys | missense_variant | 0.18 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568507 | p.Gln58Arg | missense_variant | 1.0 |
Rv3236c | 3613297 | c.-181C>T | upstream_gene_variant | 1.0 |
alr | 3840431 | c.990C>A | synonymous_variant | 0.2 |
clpC1 | 4040330 | c.375C>A | synonymous_variant | 0.12 |
embA | 4243933 | p.Arg234Leu | missense_variant | 0.2 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248732 | p.Val740Ala | missense_variant | 0.2 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ethA | 4327467 | p.Glu3* | stop_gained | 0.2 |
ethA | 4328157 | c.-684C>A | upstream_gene_variant | 0.15 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |