Run ID: ERR4815298
Sample name:
Date: 01-04-2023 13:47:06
Number of reads: 683227
Percentage reads mapped: 75.07
Strain: lineage4.3.4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.69 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrB | 6218 | p.Val327Leu | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491008 | c.231delC | frameshift_variant | 0.15 |
fgd1 | 491067 | p.Cys95* | stop_gained | 0.14 |
ccsA | 620406 | c.516G>T | synonymous_variant | 0.12 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.22 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.22 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.22 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.22 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.18 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.17 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.17 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.17 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.17 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.18 |
rpoC | 762483 | c.-887C>T | upstream_gene_variant | 0.18 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.2 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.15 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.15 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.13 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.12 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.12 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.11 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.12 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.17 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.15 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.23 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.25 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.31 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.26 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.28 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.33 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.31 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.31 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.18 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.22 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.22 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.24 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.24 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.22 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.21 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.21 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.22 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.22 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.19 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.2 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.2 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.22 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.22 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.4 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.4 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.31 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.31 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.31 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.25 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.2 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.25 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.4 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.29 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.25 |
rpoC | 764740 | p.Met457Ile | missense_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766141 | c.2772C>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777661 | p.Ala274Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303462 | p.Ala178Thr | missense_variant | 0.13 |
embR | 1416836 | p.Val171Ala | missense_variant | 0.13 |
embR | 1417083 | p.Asp89Tyr | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.18 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.22 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.18 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.18 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.18 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.18 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.2 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.19 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.15 |
tlyA | 1917750 | c.-190A>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918745 | c.806A>G | stop_lost&splice_region_variant | 0.11 |
katG | 2154555 | c.1557C>T | synonymous_variant | 0.5 |
PPE35 | 2168022 | p.Leu864Pro | missense_variant | 0.13 |
Rv1979c | 2222023 | p.Ala381Asp | missense_variant | 0.17 |
Rv1979c | 2223025 | p.Ala47Val | missense_variant | 0.15 |
Rv1979c | 2223047 | p.Ile40Phe | missense_variant | 0.14 |
Rv1979c | 2223236 | c.-72C>T | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746185 | p.Val472Phe | missense_variant | 0.13 |
pepQ | 2860163 | p.Arg86Trp | missense_variant | 0.11 |
thyX | 3067737 | p.Phe70Ser | missense_variant | 0.17 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087316 | p.Val166Ala | missense_variant | 0.11 |
Rv3083 | 3448563 | c.60C>T | synonymous_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568640 | p.Arg14Gly | missense_variant | 0.15 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3612548 | p.Ala190Asp | missense_variant | 0.17 |
fbiA | 3641017 | p.Pro159Thr | missense_variant | 0.2 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039592 | c.1113G>T | synonymous_variant | 0.15 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.15 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245238 | p.Asp669Gly | missense_variant | 0.11 |
embA | 4245367 | p.Arg712His | missense_variant | 0.13 |
embA | 4245387 | p.Ala719Thr | missense_variant | 0.14 |
aftB | 4267605 | p.Arg411His | missense_variant | 0.5 |
aftB | 4269276 | c.-440C>T | upstream_gene_variant | 0.25 |
aftB | 4269816 | c.-980G>T | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407599 | p.Val202Met | missense_variant | 0.14 |
gid | 4407936 | c.267T>A | synonymous_variant | 0.17 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |