Run ID: SRR5535926
Sample name:
Date: 04-04-2023 10:45:24
Number of reads: 1091208
Percentage reads mapped: 98.64
Strain: lineage1.2.2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
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 |
---|---|---|---|---|---|
rrs | 1472359 | n.514A>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674262 | p.Ile21Val | missense_variant | 0.91 | isoniazid |
katG | 2154641 | p.Gly491Cys | missense_variant | 0.18 | 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 | 8064 | p.Gly255* | stop_gained | 0.13 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.91 |
gyrA | 8564 | c.1263G>T | synonymous_variant | 0.19 |
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 | 576355 | c.1008G>T | synonymous_variant | 0.2 |
mshA | 576631 | p.Phe428Leu | missense_variant | 0.15 |
rpoB | 759928 | p.Pro41Gln | missense_variant | 0.15 |
rpoB | 761208 | p.Asp468Tyr | missense_variant | 0.12 |
rpoB | 761342 | p.Lys512Asn | missense_variant | 0.17 |
rpoB | 761704 | p.Gly633Val | missense_variant | 0.11 |
rpoB | 762731 | p.Gln975His | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763158 | p.Leu1118Met | missense_variant | 0.17 |
rpoC | 763552 | c.183C>T | synonymous_variant | 0.91 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764174 | p.Asp269Tyr | missense_variant | 0.17 |
rpoC | 764701 | c.1332C>A | synonymous_variant | 0.15 |
rpoC | 767091 | p.Arg1241His | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779625 | c.-720G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801440 | p.Ala211Val | missense_variant | 0.17 |
Rv1258c | 1407072 | p.Pro90His | missense_variant | 0.29 |
Rv1258c | 1407091 | p.Ala84Thr | missense_variant | 0.5 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473087 | n.1242A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473717 | n.60G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476486 | n.2830delG | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673545 | p.Ala36Ser | missense_variant | 0.33 |
inhA | 1674510 | p.Met103Ile | missense_variant | 0.25 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.14 |
tlyA | 1917952 | p.Ala5Ser | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918072 | p.Ala45Ser | missense_variant | 0.2 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
ndh | 2102286 | p.Asp253Tyr | missense_variant | 0.18 |
ndh | 2102589 | p.Leu152Met | missense_variant | 0.15 |
ndh | 2103089 | c.-47C>G | upstream_gene_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154961 | p.Leu384Pro | missense_variant | 0.22 |
katG | 2155391 | p.Pro241Thr | missense_variant | 0.17 |
katG | 2155932 | c.180G>A | synonymous_variant | 0.15 |
PPE35 | 2167742 | c.2871C>A | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.92 |
PPE35 | 2167969 | p.Pro882Thr | missense_variant | 0.2 |
PPE35 | 2168009 | c.2604C>T | synonymous_variant | 0.17 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 0.89 |
PPE35 | 2170296 | p.Gln106Pro | missense_variant | 0.3 |
PPE35 | 2170681 | c.-69G>T | upstream_gene_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288821 | p.Gln141Lys | missense_variant | 0.13 |
pncA | 2289036 | p.Pro69Gln | missense_variant | 0.16 |
pncA | 2290109 | c.-868C>A | upstream_gene_variant | 0.25 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715156 | c.177C>A | synonymous_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
pepQ | 2859609 | c.810G>A | synonymous_variant | 0.22 |
thyA | 3074462 | p.Tyr4Asp | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.9 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474145 | p.Gly47Trp | missense_variant | 0.22 |
fprA | 3474337 | p.Met111Val | missense_variant | 0.14 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475179 | p.Glu391Asp | missense_variant | 0.19 |
fbiB | 3642632 | c.1098C>T | synonymous_variant | 0.12 |
alr | 3840582 | p.Ala280Asp | missense_variant | 0.13 |
alr | 3840666 | p.Arg252Leu | missense_variant | 0.15 |
clpC1 | 4038215 | c.2490G>T | synonymous_variant | 0.12 |
clpC1 | 4040513 | p.Glu64Asp | missense_variant | 0.2 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 0.94 |
panD | 4044037 | p.Gly82Val | missense_variant | 0.15 |
embC | 4240162 | c.300C>T | synonymous_variant | 0.88 |
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 | 4245478 | p.Met749Arg | missense_variant | 0.15 |
embA | 4245670 | p.Ala813Gly | missense_variant | 1.0 |
embB | 4245794 | c.-720G>T | upstream_gene_variant | 0.14 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246979 | p.Gly156Cys | missense_variant | 1.0 |
embB | 4247113 | c.600G>T | synonymous_variant | 0.14 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249652 | p.His1047Asn | missense_variant | 0.17 |
aftB | 4267960 | p.Val293Met | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326080 | p.Ile465Asn | missense_variant | 0.12 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethA | 4327420 | p.Ser18Arg | missense_variant | 0.11 |
ethA | 4328461 | c.-988C>T | upstream_gene_variant | 0.13 |
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 | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |