Run ID: ERR2228831
Sample name:
Date: 31-03-2023 16:22:18
Number of reads: 390774
Percentage reads mapped: 99.34
Strain: lineage4.8
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761004 | p.Thr400Ala | missense_variant | 0.4 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5056 | c.-184A>T | upstream_gene_variant | 0.5 |
gyrB | 5302 | p.Glu21Asp | missense_variant | 0.5 |
gyrB | 6356 | p.Thr373Ser | missense_variant | 0.5 |
gyrA | 7346 | c.45C>T | synonymous_variant | 0.2 |
gyrA | 7349 | p.Glu16Asp | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7549 | p.Asn83Ile | missense_variant | 0.18 |
gyrA | 9157 | p.Asp619Ala | missense_variant | 0.4 |
gyrA | 9757 | p.Ala819Asp | missense_variant | 0.2 |
fgd1 | 490892 | p.Val37Gly | missense_variant | 0.5 |
fgd1 | 491769 | c.987A>C | synonymous_variant | 0.43 |
mshA | 575260 | c.-88A>C | upstream_gene_variant | 0.2 |
mshA | 575617 | c.270C>T | synonymous_variant | 0.22 |
mshA | 575900 | p.Asn185Asp | missense_variant | 0.15 |
mshA | 576468 | p.Val374Gly | missense_variant | 0.3 |
ccsA | 619964 | p.Leu25Arg | missense_variant | 0.25 |
ccsA | 620132 | p.Leu81Arg | missense_variant | 0.25 |
ccsA | 620380 | p.Met164Leu | missense_variant | 0.25 |
ccsA | 620533 | p.Met215Leu | missense_variant | 0.4 |
ccsA | 620713 | p.Tyr275Asp | missense_variant | 0.25 |
rpoB | 760740 | p.Lys312* | stop_gained | 0.5 |
rpoB | 760887 | p.Thr361Pro | missense_variant | 0.27 |
rpoB | 760900 | p.Asp365Ala | missense_variant | 0.33 |
rpoB | 761044 | p.Asn413Ile | missense_variant | 0.33 |
rpoB | 762766 | p.Leu987Arg | missense_variant | 0.4 |
rpoC | 762854 | c.-516G>A | upstream_gene_variant | 0.14 |
rpoB | 763036 | p.Tyr1077Cys | missense_variant | 0.22 |
rpoC | 763974 | p.Glu202Ala | missense_variant | 0.27 |
rpoC | 765085 | c.1716T>G | synonymous_variant | 0.29 |
rpoC | 765615 | p.Tyr749Phe | missense_variant | 0.33 |
rpoC | 765713 | p.Thr782Ser | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777113 | p.Met456Ile | missense_variant | 0.22 |
mmpL5 | 777166 | p.Ser439Thr | missense_variant | 0.25 |
mmpL5 | 777479 | p.Thr334Pro | missense_variant | 0.29 |
mmpL5 | 778954 | c.-474T>C | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781396 | c.-164T>G | upstream_gene_variant | 0.22 |
fbiC | 1303295 | p.Tyr122Phe | missense_variant | 0.29 |
fbiC | 1303553 | p.Ala208Glu | missense_variant | 0.4 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303831 | p.Thr301Ala | missense_variant | 0.22 |
fbiC | 1303997 | p.Gly356Asp | missense_variant | 0.22 |
fbiC | 1304210 | p.Asp427Ala | missense_variant | 0.22 |
fbiC | 1304805 | c.1875G>A | synonymous_variant | 0.33 |
fbiC | 1305030 | c.2100G>T | synonymous_variant | 0.4 |
fbiC | 1305413 | p.Lys828Met | missense_variant | 0.18 |
fbiC | 1305415 | p.Thr829Pro | missense_variant | 0.27 |
Rv1258c | 1406226 | p.Asp372Ala | missense_variant | 0.38 |
Rv1258c | 1406551 | p.Leu264Val | missense_variant | 0.33 |
embR | 1416826 | p.His174Gln | missense_variant | 0.2 |
embR | 1417277 | p.Asp24Ala | missense_variant | 1.0 |
atpE | 1460948 | c.-97A>T | upstream_gene_variant | 0.67 |
atpE | 1460970 | c.-75A>T | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472903 | n.1058A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473418 | n.-240G>C | upstream_gene_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475744 | n.2087A>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673159 | c.-281T>G | upstream_gene_variant | 0.5 |
rpsA | 1833359 | c.-183T>G | upstream_gene_variant | 0.4 |
rpsA | 1833517 | c.-25A>T | upstream_gene_variant | 0.43 |
rpsA | 1833541 | c.-1T>A | upstream_gene_variant | 0.29 |
rpsA | 1833543 | c.2T>A | start_lost | 0.29 |
rpsA | 1834320 | p.Val260Gly | missense_variant | 0.29 |
rpsA | 1834609 | c.1068T>G | synonymous_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918607 | p.Val223Gly | missense_variant | 0.33 |
katG | 2154622 | p.Ile497Thr | missense_variant | 0.4 |
katG | 2156297 | c.-186T>G | upstream_gene_variant | 0.75 |
katG | 2156391 | c.-280T>G | upstream_gene_variant | 0.4 |
PPE35 | 2168114 | c.2499T>A | synonymous_variant | 0.4 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169013 | p.Val534Leu | missense_variant | 0.5 |
PPE35 | 2169219 | p.Leu465Gln | missense_variant | 0.5 |
PPE35 | 2169725 | p.Asn296Lys | missense_variant | 0.33 |
PPE35 | 2169748 | p.Ile289Phe | missense_variant | 0.33 |
PPE35 | 2169884 | c.729T>A | synonymous_variant | 0.25 |
PPE35 | 2170227 | p.Asn129Ile | missense_variant | 0.5 |
PPE35 | 2170351 | p.Thr88Ala | missense_variant | 0.4 |
PPE35 | 2170746 | c.-134A>T | upstream_gene_variant | 0.18 |
Rv1979c | 2221878 | c.1287A>T | synonymous_variant | 1.0 |
Rv1979c | 2222101 | p.Ile355Asn | missense_variant | 0.4 |
Rv1979c | 2222596 | p.Val190Glu | missense_variant | 0.5 |
Rv1979c | 2222786 | p.Trp127Gly | missense_variant | 0.22 |
Rv1979c | 2223064 | p.Leu34Gln | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288862 | p.Glu127Val | missense_variant | 0.33 |
pncA | 2289405 | c.-164A>T | upstream_gene_variant | 0.33 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.5 |
kasA | 2518663 | c.549T>G | synonymous_variant | 0.27 |
kasA | 2518898 | p.Leu262Val | missense_variant | 0.15 |
eis | 2714283 | p.Glu350Asp | missense_variant | 0.29 |
eis | 2714515 | p.Asp273Ala | missense_variant | 0.5 |
eis | 2715168 | c.165T>G | synonymous_variant | 0.33 |
folC | 2746331 | p.Glu423Ala | missense_variant | 0.2 |
folC | 2746711 | p.Glu296Asp | missense_variant | 0.43 |
folC | 2746865 | p.Leu245Arg | missense_variant | 0.5 |
folC | 2747211 | p.Leu130Val | missense_variant | 0.29 |
ribD | 2987239 | p.Thr134Asn | missense_variant | 0.29 |
Rv2752c | 3064552 | p.Arg547Leu | missense_variant | 0.67 |
Rv2752c | 3065314 | c.875_877delCCG | disruptive_inframe_deletion | 0.5 |
Rv2752c | 3066313 | c.-122T>G | upstream_gene_variant | 0.29 |
Rv2752c | 3066350 | c.-159T>G | upstream_gene_variant | 0.33 |
Rv2752c | 3067162 | c.-971T>C | upstream_gene_variant | 0.33 |
thyX | 3067383 | p.Asn188Thr | missense_variant | 0.43 |
thyA | 3074515 | c.-44T>G | upstream_gene_variant | 0.33 |
thyA | 3074627 | c.-156T>A | upstream_gene_variant | 0.4 |
ald | 3086997 | p.Thr60Ser | missense_variant | 0.22 |
ald | 3087190 | p.Asp124Ala | missense_variant | 0.38 |
ald | 3087307 | p.Val163Gly | missense_variant | 0.25 |
ald | 3087316 | p.Val166Gly | missense_variant | 0.25 |
ald | 3087744 | p.Ser309Ala | missense_variant | 0.33 |
fprA | 3474238 | p.Phe78Ile | missense_variant | 0.33 |
fprA | 3474967 | p.Ser321Thr | missense_variant | 0.4 |
Rv3236c | 3612195 | p.Thr308Ser | missense_variant | 0.25 |
Rv3236c | 3612340 | c.777A>G | synonymous_variant | 0.33 |
Rv3236c | 3613029 | p.Leu30Val | missense_variant | 0.43 |
fbiA | 3641059 | p.Trp173Gly | missense_variant | 0.38 |
fbiA | 3641279 | p.Ile246Ser | missense_variant | 0.25 |
fbiB | 3641340 | c.-195T>C | upstream_gene_variant | 0.33 |
fbiB | 3641953 | p.Leu140Arg | missense_variant | 0.29 |
fbiB | 3641959 | p.Val142Gly | missense_variant | 0.25 |
fbiB | 3642332 | p.Phe266Leu | missense_variant | 0.25 |
fbiB | 3642385 | p.Leu284Arg | missense_variant | 0.22 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.33 |
rpoA | 3877540 | p.Tyr323Phe | missense_variant | 0.33 |
ddn | 3987079 | p.Lys79Arg | missense_variant | 0.12 |
ddn | 3987275 | p.Ile144Met | missense_variant | 0.13 |
clpC1 | 4039104 | p.Arg534Leu | missense_variant | 0.22 |
clpC1 | 4039830 | p.Leu292* | stop_gained | 0.67 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
clpC1 | 4040249 | p.Glu152Asp | missense_variant | 0.29 |
embC | 4239837 | c.-26A>G | upstream_gene_variant | 0.22 |
embC | 4240023 | p.Gln54Arg | missense_variant | 0.4 |
embC | 4241043 | p.Asn394Thr | missense_variant | 0.25 |
embC | 4241450 | p.Ser530Ala | missense_variant | 0.36 |
embC | 4242146 | p.Asn762Tyr | missense_variant | 0.22 |
embC | 4242151 | c.2289A>T | synonymous_variant | 0.22 |
embC | 4242305 | p.Ile815Leu | missense_variant | 0.2 |
embC | 4242566 | p.Thr902Ala | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244118 | p.Tyr296His | missense_variant | 0.33 |
embA | 4245342 | p.Ser704Ala | missense_variant | 0.25 |
embA | 4245657 | p.Ser809Thr | missense_variant | 0.33 |
embB | 4246220 | c.-294T>C | upstream_gene_variant | 0.22 |
embB | 4246226 | c.-288C>T | upstream_gene_variant | 0.22 |
embB | 4246265 | c.-249C>T | upstream_gene_variant | 0.33 |
embB | 4247777 | p.Ser422Ala | missense_variant | 0.19 |
embB | 4247920 | c.1407T>A | synonymous_variant | 0.4 |
embB | 4249659 | p.Met1049Lys | missense_variant | 0.29 |
aftB | 4267473 | p.Gly455Val | missense_variant | 0.25 |
aftB | 4267572 | p.His422Pro | missense_variant | 0.22 |
ubiA | 4269388 | p.Glu149Val | missense_variant | 0.29 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.18 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.18 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.2 |
ethR | 4327288 | c.-261T>A | upstream_gene_variant | 0.5 |
whiB6 | 4338280 | p.Ile81Asn | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408430 | c.-228G>T | upstream_gene_variant | 0.22 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |