Run ID: SRR4035752
Sample name:
Date: 04-04-2023 07:16:42
Number of reads: 1610910
Percentage reads mapped: 99.46
Strain: lineage4.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154987 | c.1124delC | frameshift_variant | 0.17 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5096 | c.-144A>T | upstream_gene_variant | 0.15 |
gyrB | 5700 | p.Glu154Gly | missense_variant | 0.11 |
gyrB | 7200 | p.Glu654Gly | missense_variant | 0.12 |
gyrA | 7252 | c.-50G>A | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8364 | p.Thr355Ala | missense_variant | 0.11 |
gyrA | 8377 | p.Asp359Gly | missense_variant | 0.12 |
gyrA | 8390 | c.1089C>T | synonymous_variant | 0.15 |
gyrA | 9051 | p.Leu584Met | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9736 | p.Leu812Pro | missense_variant | 0.12 |
fgd1 | 491254 | p.Lys158Glu | missense_variant | 0.15 |
fgd1 | 491327 | p.Ala182Val | missense_variant | 0.18 |
fgd1 | 491485 | p.Tyr235His | missense_variant | 0.14 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575709 | p.Asp121Val | missense_variant | 0.13 |
mshA | 575768 | p.Ala141Ser | missense_variant | 0.22 |
ccsA | 620047 | p.Ser53Pro | missense_variant | 0.11 |
ccsA | 620336 | p.Leu149Pro | missense_variant | 0.13 |
rpoB | 760098 | p.Ser98Thr | missense_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 762560 | c.-810A>G | upstream_gene_variant | 0.11 |
rpoC | 763333 | c.-37G>A | upstream_gene_variant | 0.17 |
rpoC | 763516 | c.147G>A | synonymous_variant | 0.12 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764587 | c.1218C>T | synonymous_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765643 | c.2274G>A | synonymous_variant | 0.17 |
rpoC | 766090 | c.2721C>T | synonymous_variant | 0.13 |
rpoC | 766360 | c.2991C>T | synonymous_variant | 0.13 |
rpoC | 766596 | p.Val1076Ala | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776906 | p.Gln525His | missense_variant | 0.1 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303637 | p.Lys236Arg | missense_variant | 0.12 |
fbiC | 1304068 | p.Val380Ile | missense_variant | 0.15 |
fbiC | 1304448 | c.1518C>A | synonymous_variant | 0.16 |
Rv1258c | 1406098 | c.1242delC | frameshift_variant | 0.14 |
Rv1258c | 1407108 | p.Ala78Val | missense_variant | 0.15 |
Rv1258c | 1407138 | p.Tyr68Cys | missense_variant | 0.13 |
atpE | 1461094 | p.Met17Thr | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472210 | n.367delT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472728 | n.883G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472753 | n.908A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473017 | n.1172A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474367 | n.710T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474398 | n.741A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474791 | n.1134C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474911 | n.1254G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475434 | n.1777G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476331 | n.2674G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476543 | n.2886G>C | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673822 | p.Gln128Leu | missense_variant | 0.15 |
inhA | 1673946 | c.-256C>T | upstream_gene_variant | 0.13 |
inhA | 1674714 | c.513C>T | synonymous_variant | 0.15 |
rpsA | 1833645 | p.Asp35Val | missense_variant | 0.18 |
rpsA | 1833656 | p.Val39Ile | missense_variant | 0.22 |
rpsA | 1833807 | p.Leu89Pro | missense_variant | 0.11 |
rpsA | 1834398 | p.His286Leu | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918535 | p.His199Arg | missense_variant | 0.12 |
katG | 2156329 | c.-218C>T | upstream_gene_variant | 0.12 |
PPE35 | 2168025 | p.Ala863Val | missense_variant | 0.14 |
PPE35 | 2168304 | p.Thr770Met | missense_variant | 0.17 |
PPE35 | 2168480 | c.2133C>T | synonymous_variant | 0.13 |
PPE35 | 2169291 | p.Val441Asp | missense_variant | 0.18 |
PPE35 | 2170263 | p.Leu117His | missense_variant | 0.15 |
Rv1979c | 2222425 | p.Ala247Glu | missense_variant | 0.15 |
Rv1979c | 2223073 | p.Gly31Asp | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518947 | p.Val278Glu | missense_variant | 0.12 |
eis | 2714434 | p.Asn300Ser | missense_variant | 0.11 |
eis | 2714491 | p.Asp281Val | missense_variant | 0.14 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.13 |
pepQ | 2859608 | p.Arg271Trp | missense_variant | 0.15 |
pepQ | 2860487 | c.-69G>T | upstream_gene_variant | 0.14 |
ribD | 2987385 | p.Ala183Ser | missense_variant | 0.18 |
ribD | 2987445 | p.Val203Ile | missense_variant | 0.22 |
thyX | 3067331 | c.615C>T | synonymous_variant | 0.18 |
thyA | 3073870 | c.601delT | frameshift_variant | 0.15 |
thyA | 3074480 | c.-9G>A | upstream_gene_variant | 0.17 |
thyA | 3074492 | c.-21T>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087717 | p.Asn300Asp | missense_variant | 0.12 |
ald | 3087724 | p.Pro302Arg | missense_variant | 0.11 |
ald | 3087927 | c.1108C>T | synonymous_variant | 0.12 |
Rv3083 | 3448979 | p.Phe159Tyr | missense_variant | 0.14 |
Rv3083 | 3449115 | c.612C>A | synonymous_variant | 0.14 |
Rv3083 | 3449125 | p.Thr208Ala | missense_variant | 0.15 |
Rv3083 | 3449336 | p.Gly278Asp | missense_variant | 0.2 |
Rv3083 | 3449896 | p.His465Tyr | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
fbiB | 3640788 | c.-747T>C | upstream_gene_variant | 0.14 |
fbiB | 3642071 | c.537C>G | synonymous_variant | 0.12 |
fbiB | 3642391 | p.Ala286Glu | missense_variant | 0.12 |
fbiB | 3642395 | c.861A>G | synonymous_variant | 0.13 |
fbiB | 3642805 | p.Ile424Thr | missense_variant | 0.14 |
alr | 3840723 | p.His233Leu | missense_variant | 0.14 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.27 |
ddn | 3986959 | p.Gly39Asp | missense_variant | 0.2 |
clpC1 | 4038855 | p.Lys617Thr | missense_variant | 0.11 |
clpC1 | 4038884 | c.1821C>A | synonymous_variant | 0.15 |
embC | 4240012 | c.152delC | frameshift_variant | 0.12 |
embC | 4240726 | c.864G>T | synonymous_variant | 0.2 |
embC | 4240806 | p.Arg315His | missense_variant | 0.25 |
embC | 4241705 | p.Ser615Pro | missense_variant | 0.12 |
embA | 4242421 | c.-812C>T | upstream_gene_variant | 0.15 |
embC | 4242425 | p.Arg855* | stop_gained | 0.15 |
embC | 4242495 | p.Asp878Gly | missense_variant | 0.13 |
embA | 4242559 | c.-674G>A | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244767 | c.1539delG | frameshift_variant | 0.14 |
embA | 4245434 | c.2202G>A | synonymous_variant | 0.18 |
embB | 4246913 | p.Ser134Pro | missense_variant | 0.15 |
embB | 4246942 | c.429G>A | synonymous_variant | 0.14 |
embB | 4246947 | p.Cys145Tyr | missense_variant | 0.21 |
aftB | 4267836 | p.Met334Lys | missense_variant | 0.12 |
aftB | 4268705 | c.132C>G | synonymous_variant | 0.15 |
ethA | 4327176 | p.Phe100Leu | missense_variant | 0.11 |
ethR | 4328072 | p.Leu175Pro | missense_variant | 0.1 |
whiB6 | 4338525 | c.-4G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |