Run ID: ERR4821334
Sample name:
Date: 01-04-2023 17:11:56
Number of reads: 2540797
Percentage reads mapped: 72.76
Strain: lineage4.1.3
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 |
lineage4.1.3 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.1 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.18 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.59 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.17 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761123 | c.1317G>C | synonymous_variant | 0.1 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.11 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.1 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.13 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.15 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.15 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.15 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.22 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.11 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.24 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.18 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.26 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.16 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.1 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.17 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.19 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.16 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.19 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.16 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.12 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.1 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.14 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.25 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.21 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.22 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.19 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.17 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.17 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.17 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.18 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.17 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.17 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.23 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.28 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.11 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.12 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.12 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.13 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.1 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.24 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.2 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.22 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.22 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.22 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.22 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.2 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.23 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.21 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.27 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.23 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.11 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.14 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.17 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.16 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.16 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.18 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.16 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.17 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.16 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.16 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.11 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.38 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475834 | n.2177T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.44 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.12 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.15 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.13 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.16 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.14 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.18 |
rpsA | 1833751 | c.210C>T | synonymous_variant | 0.15 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.16 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.18 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.23 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.16 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.18 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.17 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.14 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039804 | p.Ala301Ser | missense_variant | 0.2 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.23 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.21 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.24 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.24 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.31 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.38 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.35 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.35 |
clpC1 | 4039889 | c.816G>T | synonymous_variant | 0.28 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.2 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.11 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.11 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.12 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
aftB | 4268683 | p.Gly52Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |