Run ID: ERR4816604
Sample name:
Date: 01-04-2023 14:31:29
Number of reads: 716110
Percentage reads mapped: 91.7
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.22 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.11 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.22 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.22 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.2 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.11 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6907 | c.-395C>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7864 | p.Asn188Ile | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9648 | p.Val783Met | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.18 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.14 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.25 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.12 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.19 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.11 |
rpoB | 761159 | c.1353G>A | synonymous_variant | 0.12 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.18 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.11 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.11 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.11 |
rpoB | 761192 | c.1386C>A | synonymous_variant | 0.11 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.11 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.1 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.11 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.11 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.11 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.12 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.12 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.1 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763896 | p.Lys176Arg | missense_variant | 0.12 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.11 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.16 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.1 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.14 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.1 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.14 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766936 | p.Glu1189Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.15 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.38 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.12 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.13 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.13 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.13 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.13 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.14 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.11 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288929 | p.Gly105Ser | missense_variant | 0.14 |
pncA | 2289131 | c.111A>G | synonymous_variant | 0.12 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518766 | p.Thr218Ala | missense_variant | 0.13 |
ribD | 2987112 | p.Gly92Ser | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448924 | p.Gly141Ser | missense_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
ddn | 3986861 | c.18G>C | synonymous_variant | 0.11 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |