Run ID: ERR4815797
Sample name:
Date: 01-04-2023 14:04:12
Number of reads: 307607
Percentage reads mapped: 97.34
Strain: lineage1.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
ethA | 4326791 | p.Trp228* | stop_gained | 1.0 | ethionamide |
gid | 4408087 | c.115delC | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6175 | c.936G>A | synonymous_variant | 0.22 |
gyrB | 6895 | p.Met552Ile | missense_variant | 0.33 |
gyrB | 6905 | p.Ile556Val | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7679 | c.378G>A | synonymous_variant | 0.4 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575433 | c.89delC | frameshift_variant | 0.2 |
mshA | 575906 | p.Ala187Thr | missense_variant | 0.2 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoB | 761218 | p.Pro471Gln | missense_variant | 0.33 |
rpoB | 761330 | c.1524G>A | synonymous_variant | 0.29 |
rpoC | 762524 | c.-846G>A | upstream_gene_variant | 0.5 |
rpoC | 763536 | p.Arg56Leu | missense_variant | 0.25 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764574 | p.Leu402Pro | missense_variant | 0.33 |
rpoC | 765990 | p.Thr874Ile | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800625 | c.-184A>T | upstream_gene_variant | 1.0 |
fbiC | 1304121 | c.1192delT | frameshift_variant | 0.22 |
fbiC | 1304260 | c.1334delG | frameshift_variant | 0.4 |
Rv1258c | 1406470 | p.Met291Val | missense_variant | 0.18 |
Rv1258c | 1406533 | p.Gly270Ser | missense_variant | 0.13 |
Rv1258c | 1406930 | p.Trp137* | stop_gained | 0.29 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.5 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.5 |
embR | 1416920 | p.Arg143Lys | missense_variant | 0.22 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417060 | c.288A>G | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833414 | c.-127delT | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102024 | c.1018delG | frameshift_variant | 1.0 |
katG | 2154217 | p.Arg632Leu | missense_variant | 0.33 |
katG | 2155737 | c.375C>G | synonymous_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2170462 | p.Gly51Arg | missense_variant | 0.25 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223243 | c.-79G>A | upstream_gene_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289585 | c.-345dupT | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518584 | p.Gln157Arg | missense_variant | 0.22 |
ahpC | 2725933 | c.-260G>T | upstream_gene_variant | 0.18 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3066122 | p.Ile24Val | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086916 | p.Val33Met | missense_variant | 0.33 |
fbiD | 3339657 | c.540A>G | synonymous_variant | 0.17 |
Rv3083 | 3448675 | p.Asp58Asn | missense_variant | 0.67 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448889 | p.Arg129Gln | missense_variant | 0.25 |
Rv3083 | 3448950 | c.447T>C | synonymous_variant | 0.2 |
Rv3083 | 3449982 | c.1479G>A | synonymous_variant | 0.12 |
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 |
fbiA | 3640976 | p.Ala145Val | missense_variant | 0.25 |
alr | 3840896 | p.Met175Ile | missense_variant | 0.33 |
alr | 3841220 | c.201C>T | synonymous_variant | 0.22 |
ddn | 3986726 | c.-118G>A | upstream_gene_variant | 0.25 |
ddn | 3986807 | c.-37G>A | upstream_gene_variant | 0.18 |
ddn | 3986815 | c.-29_-28insGC | upstream_gene_variant | 0.18 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.5 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040706 | c.-2C>T | upstream_gene_variant | 0.67 |
embC | 4239755 | c.-108C>T | upstream_gene_variant | 0.22 |
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 | 4243583 | c.351G>T | synonymous_variant | 0.22 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245819 | p.Ser863Gly | missense_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246312 | p.Gly1027Asp | missense_variant | 0.2 |
embB | 4246801 | c.288G>T | synonymous_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248015 | p.Thr501Met | missense_variant | 0.33 |
embB | 4248055 | c.1542G>A | synonymous_variant | 0.22 |
embB | 4248835 | p.Trp774* | stop_gained | 0.29 |
embB | 4248853 | c.2340G>T | synonymous_variant | 0.29 |
embB | 4249149 | p.Ala879Val | missense_variant | 0.29 |
embB | 4249250 | c.2739delC | frameshift_variant | 0.22 |
embB | 4249440 | p.Glu976Val | missense_variant | 0.2 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327389 | p.Thr29Ser | missense_variant | 0.33 |
ethR | 4327906 | p.Val120Ile | missense_variant | 0.25 |
ethA | 4328324 | c.-851A>G | upstream_gene_variant | 0.33 |
whiB6 | 4338270 | c.252A>G | synonymous_variant | 0.4 |
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 |