Run ID: SRR13861686
Sample name:
Date: 03-04-2023 09:38:05
Number of reads: 258886
Percentage reads mapped: 25.91
Strain: lineage4.9
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 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.18 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6209 | c.970C>T | synonymous_variant | 0.22 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.2 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.2 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.22 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.18 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.18 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.18 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.18 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.18 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.18 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.18 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.17 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.17 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.18 |
gyrA | 8020 | p.Thr240Ile | missense_variant | 0.18 |
gyrA | 8024 | c.723T>C | synonymous_variant | 0.18 |
gyrA | 8027 | c.726T>C | synonymous_variant | 0.2 |
gyrA | 8036 | c.735A>G | synonymous_variant | 0.22 |
gyrA | 8039 | c.738T>C | synonymous_variant | 0.22 |
gyrA | 8048 | c.747C>T | synonymous_variant | 0.2 |
gyrA | 8054 | c.753T>C | synonymous_variant | 0.2 |
gyrA | 8057 | c.756A>G | synonymous_variant | 0.2 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.18 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.18 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.2 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.2 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.2 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.2 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.22 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.25 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.25 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.25 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.33 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.33 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.33 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.33 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.33 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.33 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.29 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.29 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.25 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.25 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.25 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.25 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.22 |
ccsA | 620331 | c.441C>T | synonymous_variant | 0.15 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.17 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.15 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.14 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.14 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.14 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.14 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.14 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.18 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.2 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.17 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.17 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.22 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.33 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.43 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.5 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.43 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.33 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.33 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.33 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.33 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.33 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.5 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.4 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.33 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.33 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.33 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.33 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.29 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.25 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.25 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.25 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.25 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.29 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.25 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.25 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.25 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.25 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.25 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.18 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.18 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.18 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.2 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.2 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.2 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.2 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.2 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.18 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.18 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.18 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.18 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.18 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.18 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.18 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.18 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.18 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.18 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.18 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.18 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.18 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.18 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.27 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.22 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.2 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.3 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.3 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.2 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.33 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.22 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.29 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.29 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.25 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.25 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.22 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.25 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.25 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.22 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.2 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.3 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.15 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.17 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.17 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.14 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.12 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.3 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.25 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.25 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.25 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.25 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.22 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.22 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.22 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.2 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.2 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.25 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.25 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.2 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.2 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.2 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.25 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.22 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.22 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.29 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.25 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.2 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.3 |
inhA | 1674216 | c.15G>C | synonymous_variant | 0.29 |
inhA | 1674231 | c.30T>C | synonymous_variant | 0.29 |
inhA | 1674237 | c.36T>C | synonymous_variant | 0.29 |
inhA | 1674239 | p.Ser13Thr | missense_variant | 0.29 |
inhA | 1674243 | c.42A>G | synonymous_variant | 0.29 |
inhA | 1674279 | c.78A>C | synonymous_variant | 0.33 |
inhA | 1674280 | p.Arg27Lys | missense_variant | 0.33 |
inhA | 1674285 | c.84A>G | synonymous_variant | 0.33 |
inhA | 1674301 | c.102_103delCC | frameshift_variant | 0.33 |
inhA | 1674307 | c.106C>T | synonymous_variant | 0.33 |
inhA | 1674315 | c.114C>G | synonymous_variant | 0.29 |
inhA | 1674321 | c.120G>C | synonymous_variant | 0.29 |
rpsA | 1833851 | p.Lys104Gln | missense_variant | 1.0 |
Rv1979c | 2223241 | c.-77C>G | upstream_gene_variant | 1.0 |
pncA | 2289811 | c.-570C>T | upstream_gene_variant | 1.0 |
pncA | 2289994 | c.-753A>C | upstream_gene_variant | 1.0 |
kasA | 2518301 | p.His63Asp | missense_variant | 1.0 |
pepQ | 2859859 | p.Ala187Glu | missense_variant | 1.0 |
Rv2752c | 3064886 | p.Ala436Pro | missense_variant | 1.0 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
Rv3083 | 3449104 | p.Pro201Ala | missense_variant | 1.0 |
Rv3236c | 3612337 | c.779delG | frameshift_variant | 1.0 |
fbiB | 3641723 | c.189T>C | synonymous_variant | 1.0 |
rpoA | 3877740 | c.768G>T | synonymous_variant | 1.0 |
embC | 4241005 | c.1143G>T | synonymous_variant | 1.0 |
embC | 4241081 | c.1220delT | frameshift_variant | 1.0 |
embC | 4242746 | p.Pro962Ser | missense_variant | 1.0 |
embA | 4243969 | p.Val246Ala | missense_variant | 1.0 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.22 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.22 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.22 |