Run ID: ERR2228804
Sample name:
Date: 31-03-2023 16:21:31
Number of reads: 414924
Percentage reads mapped: 99.42
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 | 761114 | p.Gln436His | missense_variant | 0.2 | rifampicin |
pncA | 2289050 | p.Tyr64* | stop_gained | 0.4 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7957 | p.Val219Gly | missense_variant | 0.33 |
gyrA | 9519 | p.Tyr740Asn | missense_variant | 0.25 |
gyrA | 9561 | p.Met754Leu | missense_variant | 0.17 |
mshA | 576237 | p.Val297Ala | missense_variant | 0.18 |
ccsA | 619884 | c.-7A>G | upstream_gene_variant | 0.29 |
rpoB | 760650 | p.Thr282Pro | missense_variant | 0.2 |
rpoB | 762214 | p.Lys803Met | missense_variant | 0.4 |
rpoB | 762276 | p.Arg824Ser | missense_variant | 0.25 |
rpoC | 765057 | p.Asn563Ile | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776625 | p.Asn619Thr | missense_variant | 0.2 |
mmpL5 | 777250 | p.Tyr411Asp | missense_variant | 0.2 |
mmpL5 | 777369 | p.Lys371Thr | missense_variant | 0.4 |
mmpL5 | 777988 | p.Ser165Thr | missense_variant | 0.4 |
mmpL5 | 777999 | p.Leu161Gln | missense_variant | 0.29 |
mmpL5 | 778412 | p.Phe23Leu | missense_variant | 0.33 |
mmpR5 | 779066 | p.Tyr26Phe | missense_variant | 0.5 |
mmpR5 | 779330 | p.Leu114Gln | missense_variant | 0.33 |
rpsL | 781371 | c.-189T>G | upstream_gene_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781918 | p.Lys120Met | missense_variant | 0.33 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303803 | c.873C>A | synonymous_variant | 0.22 |
fbiC | 1304971 | p.Thr681Pro | missense_variant | 0.5 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.62 |
fbiC | 1305040 | p.Ser704Ala | missense_variant | 0.44 |
Rv1258c | 1406748 | p.Lys198Thr | missense_variant | 0.3 |
embR | 1416547 | p.Lys267Asn | missense_variant | 0.33 |
embR | 1416584 | p.Leu255Gln | missense_variant | 0.25 |
embR | 1416608 | p.Leu247* | stop_gained | 0.4 |
atpE | 1461133 | p.Val30Gly | missense_variant | 0.5 |
atpE | 1461243 | p.Asn67Tyr | missense_variant | 0.4 |
rrs | 1471654 | n.-192A>T | upstream_gene_variant | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471708 | n.-138A>T | upstream_gene_variant | 0.38 |
rrs | 1471716 | n.-130T>A | upstream_gene_variant | 0.33 |
rrs | 1473004 | n.1159T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474247 | n.590A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474450 | n.793T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474532 | n.875T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475823 | n.2166A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476679 | n.3022T>A | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673258 | c.-182A>C | upstream_gene_variant | 0.25 |
fabG1 | 1673645 | p.Asp69Val | missense_variant | 0.5 |
fabG1 | 1674050 | p.Gln204Leu | missense_variant | 0.25 |
inhA | 1674395 | p.Val65Ala | missense_variant | 0.33 |
rpsA | 1833944 | p.Lys135* | stop_gained | 0.25 |
rpsA | 1834179 | p.Lys213Met | missense_variant | 0.29 |
rpsA | 1834578 | p.Val346Gly | missense_variant | 0.22 |
rpsA | 1834614 | p.Ile358Ser | missense_variant | 0.3 |
rpsA | 1834676 | p.Gly379Cys | missense_variant | 0.29 |
rpsA | 1834941 | p.Asp467Ala | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918105 | p.Thr56Pro | missense_variant | 0.22 |
tlyA | 1918221 | c.282T>G | synonymous_variant | 0.3 |
tlyA | 1918607 | p.Val223Gly | missense_variant | 0.3 |
tlyA | 1918704 | c.765A>T | synonymous_variant | 0.33 |
ndh | 2102721 | p.Tyr108Asn | missense_variant | 0.5 |
katG | 2155097 | p.Tyr339Asn | missense_variant | 0.33 |
katG | 2155760 | p.Gly118Cys | missense_variant | 0.38 |
katG | 2155785 | c.327T>G | synonymous_variant | 0.29 |
katG | 2156533 | c.-422A>C | upstream_gene_variant | 0.43 |
PPE35 | 2168710 | p.Asn635Tyr | missense_variant | 0.5 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168810 | c.1803T>A | synonymous_variant | 0.6 |
PPE35 | 2168876 | p.Phe579Leu | missense_variant | 0.5 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.25 |
PPE35 | 2170738 | c.-126A>T | upstream_gene_variant | 0.25 |
Rv1979c | 2222377 | p.Val263Asp | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288841 | p.Ala134Asp | missense_variant | 0.17 |
pncA | 2288880 | p.Arg121Leu | missense_variant | 0.18 |
pncA | 2289376 | c.-135T>G | upstream_gene_variant | 0.33 |
pncA | 2289389 | c.-148A>T | upstream_gene_variant | 0.29 |
pncA | 2289553 | c.-312C>A | upstream_gene_variant | 0.67 |
pncA | 2289594 | c.-353C>A | upstream_gene_variant | 0.29 |
pncA | 2289782 | c.-541A>C | upstream_gene_variant | 0.75 |
pncA | 2290226 | c.-985T>G | upstream_gene_variant | 0.5 |
kasA | 2518203 | p.Glu30Val | missense_variant | 0.5 |
kasA | 2518663 | c.549T>G | synonymous_variant | 0.22 |
kasA | 2519352 | p.Phe413Cys | missense_variant | 0.29 |
eis | 2714391 | c.942T>C | synonymous_variant | 0.13 |
eis | 2714562 | c.771T>A | synonymous_variant | 0.29 |
eis | 2715095 | p.Ala80Ser | missense_variant | 0.33 |
eis | 2715574 | c.-242T>C | upstream_gene_variant | 0.25 |
ahpC | 2726400 | p.Lys70* | stop_gained | 0.67 |
folC | 2746377 | p.Ser408Ala | missense_variant | 0.4 |
folC | 2746769 | p.Leu277Gln | missense_variant | 0.2 |
pepQ | 2859629 | p.Leu264Val | missense_variant | 0.43 |
ribD | 2987263 | p.Val142Gly | missense_variant | 0.25 |
Rv2752c | 3064680 | c.1512C>A | synonymous_variant | 0.33 |
Rv2752c | 3065541 | p.Glu217Asp | missense_variant | 0.5 |
thyA | 3074089 | p.Ile128Thr | missense_variant | 0.22 |
thyA | 3074278 | p.Gly65Val | missense_variant | 0.29 |
thyA | 3074318 | p.Phe52Ile | missense_variant | 0.33 |
thyA | 3074334 | c.138T>A | synonymous_variant | 0.43 |
ald | 3087277 | p.Gln153Leu | missense_variant | 0.29 |
ald | 3087906 | p.Phe363Val | missense_variant | 0.5 |
fbiD | 3339633 | c.516T>G | synonymous_variant | 0.29 |
fprA | 3474142 | p.Trp46Arg | missense_variant | 0.29 |
fprA | 3475374 | c.1368C>A | synonymous_variant | 0.33 |
Rv3236c | 3612099 | p.Ile340Phe | missense_variant | 0.29 |
Rv3236c | 3613055 | p.Leu21Arg | missense_variant | 0.2 |
Rv3236c | 3613283 | c.-167T>C | upstream_gene_variant | 0.22 |
fbiA | 3640463 | c.-80T>A | upstream_gene_variant | 0.38 |
fbiB | 3642072 | p.Arg180Ser | missense_variant | 0.25 |
fbiB | 3642201 | p.Ser223Ala | missense_variant | 0.18 |
fbiB | 3642335 | p.Ser267Arg | missense_variant | 0.2 |
fbiB | 3642717 | p.Ser395Cys | missense_variant | 0.43 |
alr | 3840408 | p.Val338Gly | missense_variant | 0.33 |
alr | 3841095 | p.Val109Gly | missense_variant | 0.29 |
alr | 3841179 | p.Ala81Asp | missense_variant | 0.22 |
alr | 3841183 | p.Thr80Pro | missense_variant | 0.3 |
alr | 3841184 | p.Gln79His | missense_variant | 0.2 |
rpoA | 3877852 | p.Phe219Ser | missense_variant | 0.29 |
rpoA | 3878171 | p.Pro113Ser | missense_variant | 0.22 |
ddn | 3986655 | c.-189A>G | upstream_gene_variant | 0.36 |
clpC1 | 4038306 | p.Val800Gly | missense_variant | 0.33 |
clpC1 | 4038334 | p.Phe791Ile | missense_variant | 0.22 |
clpC1 | 4038526 | p.Ile727Leu | missense_variant | 0.4 |
clpC1 | 4038543 | p.Gln721Pro | missense_variant | 0.33 |
clpC1 | 4039054 | p.Phe551Ile | missense_variant | 0.33 |
clpC1 | 4039714 | p.Tyr331Asn | missense_variant | 0.2 |
clpC1 | 4040409 | p.Gly99Val | missense_variant | 0.33 |
embC | 4240461 | p.Val200Gly | missense_variant | 0.36 |
embC | 4240581 | p.Leu240Arg | missense_variant | 0.3 |
embC | 4241593 | c.1731C>A | synonymous_variant | 0.25 |
embC | 4241685 | p.Val608Gly | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245121 | p.Tyr630Phe | missense_variant | 0.4 |
embA | 4246329 | p.Thr1033Pro | missense_variant | 0.33 |
embB | 4246841 | p.Asn110Tyr | missense_variant | 0.31 |
embB | 4247897 | p.Met462Leu | missense_variant | 0.22 |
embB | 4247945 | p.Leu478Val | missense_variant | 0.3 |
embB | 4248772 | c.2259A>C | synonymous_variant | 0.22 |
embB | 4249277 | p.Tyr922His | missense_variant | 0.18 |
aftB | 4267194 | p.Pro548Gln | missense_variant | 0.14 |
aftB | 4267242 | p.Leu532Gln | missense_variant | 0.18 |
aftB | 4267386 | p.His484Arg | missense_variant | 0.33 |
aftB | 4267597 | p.Tyr414Asn | missense_variant | 0.25 |
aftB | 4268799 | p.Val13Gly | missense_variant | 0.3 |
ubiA | 4269329 | p.Lys169* | stop_gained | 0.22 |
ubiA | 4269367 | p.Ala156Gly | missense_variant | 0.22 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.17 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.18 |
ethA | 4327537 | c.-64A>T | upstream_gene_variant | 0.4 |
ethR | 4328060 | p.Leu171Gln | missense_variant | 0.33 |
whiB6 | 4338223 | p.Glu100Ala | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408119 | c.84A>G | synonymous_variant | 0.43 |