Run ID: SRR6650111
Sample name:
Date: 15-08-2023 07:56:18
Number of reads: 884904
Percentage reads mapped: 99.32
Strain: lineage1.2.2.2
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 | 0.99 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.99 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.99 |
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 | 5440 | c.201A>C | synonymous_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6918 | p.His560Leu | missense_variant | 0.22 |
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 | 8423 | c.1122G>A | synonymous_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490979 | p.Asn66Thr | missense_variant | 0.18 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.24 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576698 | p.Glu451Gln | missense_variant | 0.15 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.18 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
ccsA | 619835 | c.-56G>T | upstream_gene_variant | 0.22 |
ccsA | 619844 | c.-47T>G | upstream_gene_variant | 0.3 |
ccsA | 620532 | c.642T>G | synonymous_variant | 0.18 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.2 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.27 |
ccsA | 620778 | p.Asn296Lys | missense_variant | 0.17 |
rpoB | 759611 | c.-196G>C | upstream_gene_variant | 0.21 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.21 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.23 |
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 | 764086 | c.717C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778282 | p.Asp67His | missense_variant | 0.23 |
rpsL | 781363 | c.-197T>G | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781524 | c.-36C>A | upstream_gene_variant | 0.15 |
rplC | 800963 | p.Leu52Arg | missense_variant | 0.19 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.19 |
fbiC | 1302890 | c.-41G>T | upstream_gene_variant | 1.0 |
fbiC | 1304125 | p.Val399Leu | missense_variant | 0.18 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472115 | n.270C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473927 | n.270C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473932 | n.275C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473959 | n.302T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474500 | n.843T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476176 | n.2519C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476274 | n.2617G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476313 | n.2656G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>C | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.27 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918059 | c.120C>A | synonymous_variant | 0.25 |
tlyA | 1918065 | c.126G>C | synonymous_variant | 0.22 |
ndh | 2102144 | p.Ala300Val | missense_variant | 0.14 |
ndh | 2102498 | p.Gly182Val | missense_variant | 0.15 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.47 |
ndh | 2103227 | c.-185T>C | upstream_gene_variant | 0.2 |
ndh | 2103231 | c.-189G>T | upstream_gene_variant | 0.19 |
ndh | 2103235 | c.-193C>G | upstream_gene_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167941 | p.Ser891Asn | missense_variant | 0.29 |
PPE35 | 2168028 | p.Pro862His | missense_variant | 0.17 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169299 | p.Asn438Lys | missense_variant | 0.29 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.14 |
Rv1979c | 2221919 | p.Val416Met | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289500 | c.-259A>G | upstream_gene_variant | 0.18 |
pncA | 2289511 | c.-270T>G | upstream_gene_variant | 0.18 |
pncA | 2290087 | c.-846T>G | upstream_gene_variant | 0.15 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.33 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.27 |
eis | 2714753 | p.Gln194* | stop_gained | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746745 | p.Val285Gly | missense_variant | 0.5 |
pepQ | 2859400 | p.Asp340Gly | missense_variant | 0.2 |
pepQ | 2859438 | c.981T>G | synonymous_variant | 0.38 |
ribD | 2986908 | p.Thr24Pro | missense_variant | 0.15 |
ribD | 2987316 | p.Ala160Pro | missense_variant | 0.24 |
ribD | 2987320 | p.Glu161Gly | missense_variant | 0.19 |
ribD | 2987323 | p.Val162Gly | missense_variant | 0.44 |
ribD | 2987337 | p.Gly167Arg | missense_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.28 |
fbiD | 3339608 | p.Pro164Arg | missense_variant | 0.21 |
fbiD | 3339626 | p.His170Pro | missense_variant | 0.2 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.91 |
Rv3083 | 3448745 | p.Ile81Thr | missense_variant | 0.2 |
Rv3083 | 3448757 | p.Ile85Thr | missense_variant | 0.27 |
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 | 3612557 | p.Val187Gly | missense_variant | 0.33 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.18 |
fbiB | 3642095 | c.561G>A | synonymous_variant | 0.13 |
fbiB | 3642759 | p.Arg409Gly | missense_variant | 0.2 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.24 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.22 |
embA | 4242406 | c.-827A>C | upstream_gene_variant | 0.24 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244621 | p.Leu463Phe | missense_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249738 | c.3225C>A | synonymous_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269504 | c.-668A>G | upstream_gene_variant | 0.27 |
ubiA | 4269511 | p.Val108Gly | missense_variant | 0.36 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269859 | c.-26A>C | upstream_gene_variant | 0.19 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethR | 4326898 | c.-651C>G | upstream_gene_variant | 0.21 |
ethA | 4326905 | p.Leu190Pro | missense_variant | 0.21 |
ethR | 4327813 | p.Thr89Pro | missense_variant | 0.17 |
ethR | 4327819 | p.Ala91Pro | missense_variant | 0.17 |
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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407921 | c.282A>G | synonymous_variant | 0.13 |