Run ID: SRR11972243
Sample name:
Date: 03-04-2023 05:33:19
Number of reads: 607137
Percentage reads mapped: 99.14
Strain: lineage1.1.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
lineage1.1.3.2 | Indo-Oceanic | NA | RD239 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5619 | p.Val127Glu | missense_variant | 0.12 |
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 | 8188 | p.Leu296Pro | missense_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 | 490963 | p.Val61Ile | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575470 | c.123A>G | synonymous_variant | 0.12 |
mshA | 575788 | c.441C>T | synonymous_variant | 0.12 |
ccsA | 619695 | c.-196G>A | upstream_gene_variant | 1.0 |
rpoB | 759709 | c.-98C>T | upstream_gene_variant | 0.13 |
rpoB | 762327 | p.Val841Leu | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763063 | p.Lys1086Arg | missense_variant | 0.22 |
rpoB | 763183 | p.Cys1126Tyr | missense_variant | 0.17 |
rpoC | 763339 | c.-31T>C | upstream_gene_variant | 0.18 |
rpoC | 763661 | p.Ala98Ser | missense_variant | 0.13 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
rpoC | 765570 | p.Ala734Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776778 | p.Arg568His | missense_variant | 0.12 |
mmpL5 | 777541 | p.Gly314Ser | missense_variant | 0.17 |
mmpL5 | 778314 | p.Val56Ala | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801166 | p.Gly120Ser | missense_variant | 1.0 |
fbiC | 1304429 | p.Arg500Gln | missense_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475396 | n.1739C>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834337 | p.Asp266Asn | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154225 | c.1887T>C | synonymous_variant | 0.15 |
katG | 2154638 | p.Ala492Thr | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.29 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.26 |
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 |
kasA | 2518452 | p.Gly113Asp | missense_variant | 0.14 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
pepQ | 2859721 | p.Met233Thr | missense_variant | 0.19 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087807 | p.Arg330Trp | missense_variant | 0.12 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449689 | p.Thr396Ala | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474168 | c.162G>T | synonymous_variant | 0.33 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475102 | p.Gly366Trp | missense_variant | 0.22 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475306 | p.Gly434Ser | missense_variant | 0.33 |
Rv3236c | 3612244 | c.873T>A | synonymous_variant | 0.15 |
Rv3236c | 3612797 | p.Ala107Glu | missense_variant | 0.13 |
Rv3236c | 3613210 | c.-94A>T | upstream_gene_variant | 0.12 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.13 |
rpoA | 3877579 | p.Asp310Val | missense_variant | 0.25 |
rpoA | 3878687 | c.-180A>C | upstream_gene_variant | 1.0 |
ddn | 3987089 | c.246G>A | synonymous_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240903 | c.1041C>A | synonymous_variant | 0.14 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241502 | p.Ser547* | stop_gained | 0.22 |
embC | 4241609 | p.Pro583Thr | missense_variant | 0.29 |
embC | 4241792 | p.Ser644Pro | missense_variant | 0.33 |
embC | 4241924 | p.Arg688Cys | missense_variant | 0.25 |
embC | 4242087 | p.Gln742Arg | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242666 | p.Ala935Val | missense_variant | 0.25 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244746 | p.Leu505His | missense_variant | 0.29 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247903 | p.Arg464Trp | missense_variant | 0.25 |
embB | 4249074 | p.Gln854Leu | missense_variant | 0.12 |
embB | 4249095 | p.Ala861Val | missense_variant | 0.2 |
aftB | 4268363 | p.Trp158Cys | missense_variant | 0.14 |
aftB | 4268898 | c.-62G>T | upstream_gene_variant | 0.18 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_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 | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407922 | p.Leu94Pro | missense_variant | 0.29 |
gid | 4408354 | c.-152G>A | upstream_gene_variant | 1.0 |