Run ID: ERR4769512
Sample name:
Date: 01-04-2023 06:43:10
Number of reads: 9785
Percentage reads mapped: 0.42
Strain: lineage4.9
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.67 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.67 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.67 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.67 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.67 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.67 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.67 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.67 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.67 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.67 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.67 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.67 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.5 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
rpoC | 762455 | c.-915C>T | upstream_gene_variant | 1.0 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
rpoB | 762489 | p.Val895Thr | missense_variant | 1.0 |
rpoC | 762497 | c.-873C>T | upstream_gene_variant | 1.0 |
rpoB | 762507 | p.Leu901Met | missense_variant | 1.0 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 1.0 |
rpoC | 762548 | c.-822C>T | upstream_gene_variant | 1.0 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
rpoC | 762560 | c.-810A>T | upstream_gene_variant | 1.0 |
rpoC | 762563 | c.-807G>T | upstream_gene_variant | 1.0 |
rpoC | 762569 | c.-801C>T | upstream_gene_variant | 1.0 |
rpoC | 762575 | c.-795C>G | upstream_gene_variant | 1.0 |
rpoC | 764344 | c.975C>G | synonymous_variant | 1.0 |
rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
rrs | 1472085 | n.240C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472086 | n.241T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472339 | n.494C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472600 | n.755C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472687 | n.842_843insCC | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472965 | n.1120C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472967 | n.1122G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472969 | n.1125_1126delCG | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472977 | n.1132G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472980 | n.1135G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472990 | n.1145A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473001 | n.1156G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473009 | n.1164T>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473265 | n.1420C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473311 | n.1466G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475776 | n.2119G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476621 | n.2964C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476625 | n.2968C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476637 | n.2980C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834663 | c.1122C>T | synonymous_variant | 1.0 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
rpsA | 1834678 | c.1137C>T | synonymous_variant | 1.0 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
rpsA | 1834788 | p.Ala416Gly | missense_variant | 1.0 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 1.0 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 1.0 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 1.0 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 1.0 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 1.0 |
clpC1 | 4040345 | c.360C>G | synonymous_variant | 1.0 |
clpC1 | 4040348 | c.357G>C | synonymous_variant | 1.0 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 1.0 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |