Run ID: SRR6650182
Sample name:
Date: 15-08-2023 07:58:10
Number of reads: 751644
Percentage reads mapped: 99.17
Strain: lineage1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.38 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.25 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575165 | c.-183C>T | upstream_gene_variant | 0.16 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.29 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.26 |
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 |
rpoC | 767011 | c.3642G>C | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778239 | p.Val81Gly | missense_variant | 0.33 |
mmpR5 | 779336 | p.Asp116Ala | missense_variant | 0.29 |
mmpR5 | 779346 | p.Asp119Glu | missense_variant | 0.25 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.38 |
mmpR5 | 779363 | p.Leu125Arg | missense_variant | 0.38 |
mmpR5 | 779369 | p.Asp127Ala | missense_variant | 0.33 |
mmpR5 | 779371 | p.Ala128Pro | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.22 |
embR | 1416481 | c.867G>A | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471981 | n.136C>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.67 |
Rv1979c | 2221725 | c.1440T>G | synonymous_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2714505 | c.828C>T | synonymous_variant | 1.0 |
eis | 2714559 | c.774C>G | synonymous_variant | 0.18 |
eis | 2714564 | p.Ile257Val | missense_variant | 0.18 |
eis | 2714566 | p.Leu256Pro | missense_variant | 0.2 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726269 | p.Val26Gly | missense_variant | 0.33 |
pepQ | 2859438 | c.981T>G | synonymous_variant | 0.25 |
pepQ | 2859454 | p.Val322Gly | missense_variant | 0.18 |
ribD | 2987320 | p.Glu161Gly | missense_variant | 0.18 |
ribD | 2987323 | p.Val162Gly | missense_variant | 0.18 |
ribD | 2987351 | c.513C>G | synonymous_variant | 0.2 |
Rv2752c | 3064889 | p.Lys435Glu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087914 | p.Glu365Asp | missense_variant | 0.25 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.23 |
fbiD | 3339279 | c.162T>G | synonymous_variant | 0.31 |
fbiD | 3339310 | p.Asp65His | missense_variant | 0.25 |
fbiD | 3339583 | p.Thr156Pro | missense_variant | 0.31 |
fbiD | 3339593 | p.His159Pro | missense_variant | 0.25 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.2 |
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 |
Rv3236c | 3612515 | p.Arg201His | missense_variant | 1.0 |
alr | 3841506 | c.-86A>C | upstream_gene_variant | 0.22 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.75 |
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 | 4246544 | p.Thr11Pro | missense_variant | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.6 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.6 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.6 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.4 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269486 | c.-650T>G | upstream_gene_variant | 0.25 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338635 | c.-114A>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |