Run ID: SRR6046556
Sample name:
Date: 04-04-2023 12:18:49
Number of reads: 1001515
Percentage reads mapped: 99.17
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 | 7839 | p.Gly180Ser | missense_variant | 0.12 |
gyrA | 7935 | p.Glu212Lys | missense_variant | 1.0 |
gyrA | 7943 | p.Glu214Asp | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576067 | c.720C>T | synonymous_variant | 0.14 |
mshA | 576195 | p.Val283Glu | missense_variant | 0.2 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.22 |
rpoB | 762171 | p.Glu789Lys | missense_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.11 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764656 | c.1287C>A | synonymous_variant | 0.13 |
rpoC | 766245 | p.Gln959Pro | missense_variant | 0.11 |
rpoC | 766941 | p.Arg1191His | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779243 | p.Val85Ala | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303115 | p.Ala62Val | missense_variant | 0.11 |
fbiC | 1303152 | c.222C>A | synonymous_variant | 0.11 |
fbiC | 1304246 | p.Asp439Val | missense_variant | 0.13 |
Rv1258c | 1407402 | c.-62C>T | upstream_gene_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1461143 | c.99C>T | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476766 | n.3109C>A | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102144 | p.Ala300Asp | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155309 | p.Gly268Val | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2168855 | c.1758T>A | synonymous_variant | 0.12 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.13 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.14 |
Rv1979c | 2222014 | p.Val384Ala | missense_variant | 0.11 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222395 | p.Pro257Gln | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289875 | c.-634C>A | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518391 | p.Gln93* | stop_gained | 0.14 |
eis | 2714855 | p.Gly160Ser | missense_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747547 | p.Val18Met | missense_variant | 0.13 |
pepQ | 2859347 | p.Thr358Ala | missense_variant | 0.11 |
pepQ | 2859579 | c.840G>A | synonymous_variant | 0.17 |
Rv2752c | 3064785 | c.1407G>A | synonymous_variant | 0.15 |
thyX | 3067790 | c.156C>G | synonymous_variant | 0.11 |
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 | 3474767 | p.Gly254Val | missense_variant | 0.13 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.18 |
ddn | 3986819 | c.-25A>C | upstream_gene_variant | 0.12 |
clpC1 | 4039423 | p.Ile428Val | missense_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240993 | c.1131G>T | synonymous_variant | 0.13 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241536 | c.1674A>G | synonymous_variant | 0.11 |
embC | 4241617 | p.Lys585Asn | missense_variant | 0.11 |
embC | 4242571 | p.Asp903Glu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242711 | p.Gln950Arg | missense_variant | 0.1 |
embA | 4243946 | c.714C>T | synonymous_variant | 0.15 |
embA | 4243981 | p.Ser250Asn | missense_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268038 | p.Trp267Arg | missense_variant | 0.11 |
aftB | 4268612 | c.225G>T | synonymous_variant | 0.5 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.21 |
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 | 4407808 | p.Asp132Val | missense_variant | 0.12 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |