Run ID: ERR1035353
Sample name:
Date: 31-03-2023 10:12:15
Number of reads: 3477215
Percentage reads mapped: 94.49
Strain: lineage4.4.1.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 0.99 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.98 |
lineage4.4.1.2 | Euro-American | T1 | None | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Tyr | missense_variant | 1.0 | rifampicin |
rrs | 1472361 | n.516C>T | non_coding_transcript_exon_variant | 0.12 | streptomycin |
fabG1 | 1673432 | c.-8T>G | upstream_gene_variant | 0.21 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288764 | p.Thr160Pro | missense_variant | 0.93 | pyrazinamide |
embB | 4247663 | p.Tyr384Asn | missense_variant | 0.17 | ethambutol |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5063 | c.-177C>T | upstream_gene_variant | 0.14 |
gyrB | 6060 | p.Ser274Asn | missense_variant | 0.17 |
gyrA | 6637 | c.-665T>C | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7404 | p.Val35Leu | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8047 | p.Gly249Asp | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575302 | c.-46C>T | upstream_gene_variant | 0.11 |
mshA | 576181 | p.Lys278Asn | missense_variant | 0.12 |
mshA | 576319 | c.972G>A | synonymous_variant | 0.18 |
rpoB | 761190 | p.Ala462Thr | missense_variant | 0.13 |
rpoC | 766519 | c.3150C>T | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776231 | c.2250G>A | synonymous_variant | 0.19 |
mmpL5 | 776532 | p.Ala650Val | missense_variant | 0.12 |
mmpL5 | 777379 | p.Leu368Phe | missense_variant | 0.33 |
mmpL5 | 777662 | c.819C>T | synonymous_variant | 0.12 |
mmpL5 | 778180 | p.Leu101Phe | missense_variant | 0.22 |
mmpL5 | 778195 | p.Glu96* | stop_gained | 0.2 |
mmpL5 | 778344 | p.Leu46Pro | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801061 | p.Arg85Trp | missense_variant | 0.2 |
rplC | 801115 | p.Ala103Ser | missense_variant | 0.15 |
fbiC | 1302807 | c.-124G>A | upstream_gene_variant | 0.14 |
fbiC | 1302893 | c.-38G>A | upstream_gene_variant | 0.13 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.23 |
fbiC | 1304307 | c.1377T>C | synonymous_variant | 0.12 |
fbiC | 1305102 | c.2172C>T | synonymous_variant | 0.11 |
fbiC | 1305285 | p.Gln785His | missense_variant | 0.11 |
Rv1258c | 1406559 | p.Gly261Val | missense_variant | 0.1 |
Rv1258c | 1407079 | p.Gly88Ser | missense_variant | 0.14 |
Rv1258c | 1407191 | c.150G>A | synonymous_variant | 0.14 |
Rv1258c | 1407347 | c.-7G>A | upstream_gene_variant | 0.29 |
embR | 1416468 | p.Asp294Asn | missense_variant | 0.25 |
atpE | 1461053 | c.9C>T | synonymous_variant | 0.14 |
atpE | 1461193 | p.Phe50Ser | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472042 | n.197T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473752 | n.95G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473923 | n.266C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474028 | n.371T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474029 | n.372G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475297 | n.1640C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475446 | n.1789G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476017 | n.2360G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476415 | n.2758C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.27 |
fabG1 | 1673461 | p.Gly8Trp | missense_variant | 0.2 |
rpsA | 1833426 | c.-116T>C | upstream_gene_variant | 0.15 |
rpsA | 1833966 | p.Ile142Thr | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102773 | c.270C>A | synonymous_variant | 0.12 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2154236 | p.Val626Met | missense_variant | 0.18 |
katG | 2156027 | p.Pro29Thr | missense_variant | 0.12 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 1.0 |
PPE35 | 2168831 | c.1782C>A | synonymous_variant | 0.14 |
PPE35 | 2169020 | c.1593G>T | synonymous_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.44 |
PPE35 | 2170407 | p.Ala69Val | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518239 | p.Gly42Asp | missense_variant | 0.14 |
ahpC | 2726010 | c.-183G>A | upstream_gene_variant | 0.12 |
folC | 2746660 | c.938delT | frameshift_variant | 0.12 |
pepQ | 2859548 | p.Gly291Cys | missense_variant | 0.12 |
pepQ | 2859964 | p.Ala152Val | missense_variant | 0.14 |
pepQ | 2860213 | p.Pro69Leu | missense_variant | 0.95 |
ribD | 2987228 | p.Met130Ile | missense_variant | 0.14 |
Rv2752c | 3064761 | c.1431C>T | synonymous_variant | 0.15 |
Rv2752c | 3066007 | p.Pro62Leu | missense_variant | 0.15 |
Rv2752c | 3066170 | p.Pro8Ser | missense_variant | 0.13 |
Rv2752c | 3066299 | c.-108C>T | upstream_gene_variant | 0.18 |
Rv2752c | 3066354 | c.-163G>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087776 | c.957G>A | synonymous_variant | 0.12 |
fbiD | 3339702 | c.585G>A | synonymous_variant | 0.12 |
fbiD | 3339730 | p.Pro205Ser | missense_variant | 0.12 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3448859 | p.Ala119Glu | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474376 | p.Ala124Thr | missense_variant | 0.14 |
Rv3236c | 3611992 | c.1125T>C | synonymous_variant | 0.12 |
Rv3236c | 3612401 | p.Ser239Leu | missense_variant | 0.11 |
fbiB | 3641543 | c.9C>T | synonymous_variant | 0.18 |
fbiB | 3641628 | p.Ala32Thr | missense_variant | 0.13 |
fbiB | 3641643 | p.Ala37Thr | missense_variant | 0.12 |
fbiB | 3641660 | c.126C>T | synonymous_variant | 0.14 |
fbiB | 3641679 | p.Thr49Ser | missense_variant | 0.12 |
fbiB | 3641721 | p.Ala63Thr | missense_variant | 0.14 |
fbiB | 3641727 | p.Glu65Lys | missense_variant | 0.14 |
fbiB | 3642101 | c.567C>T | synonymous_variant | 0.17 |
alr | 3841516 | c.-96G>A | upstream_gene_variant | 0.2 |
ddn | 3986775 | c.-69A>T | upstream_gene_variant | 0.25 |
clpC1 | 4038295 | p.Val804Met | missense_variant | 0.22 |
clpC1 | 4039046 | c.1659C>T | synonymous_variant | 0.18 |
clpC1 | 4039751 | p.Gln318His | missense_variant | 0.11 |
panD | 4044059 | p.Ala75Thr | missense_variant | 0.11 |
embC | 4240988 | p.Ala376Thr | missense_variant | 0.14 |
embC | 4241723 | p.Val621Met | missense_variant | 0.14 |
embC | 4241743 | c.1881C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244476 | p.Ala415Val | missense_variant | 0.12 |
embA | 4245787 | p.Ala852Val | missense_variant | 0.22 |
embB | 4246711 | c.198C>T | synonymous_variant | 0.2 |
embB | 4248399 | p.Leu629Pro | missense_variant | 0.13 |
embB | 4248820 | c.2307C>T | synonymous_variant | 0.14 |
embB | 4249012 | c.2499G>A | synonymous_variant | 1.0 |
embB | 4249405 | c.2892C>T | synonymous_variant | 0.13 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.13 |
aftB | 4267143 | p.Ala565Val | missense_variant | 0.12 |
ubiA | 4269173 | p.Val221Ile | missense_variant | 0.14 |
aftB | 4269594 | c.-758A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338334 | p.Ala63Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407630 | c.573T>C | synonymous_variant | 0.1 |
gid | 4408384 | c.-182G>A | upstream_gene_variant | 0.12 |