Run ID: ERR4814748
Sample name:
Date: 01-04-2023 13:28:12
Number of reads: 1295576
Percentage reads mapped: 62.97
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5706 | p.Leu156Arg | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 761552 | c.1746G>C | synonymous_variant | 0.1 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.11 |
rpoB | 761559 | p.Thr585Ala | missense_variant | 0.1 |
rpoB | 761567 | p.Met587Ile | missense_variant | 0.1 |
rpoB | 761600 | c.1794T>A | synonymous_variant | 0.11 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.12 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.1 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.13 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.12 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.1 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.12 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.12 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.15 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.11 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.12 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.11 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.11 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.14 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.14 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.16 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.12 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.12 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.12 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.13 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.13 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.16 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.32 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.33 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.29 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.3 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.29 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.26 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.26 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.26 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.27 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.27 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.23 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.23 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.15 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.15 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.17 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.18 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.4 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.43 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.37 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.48 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.48 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.43 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.42 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.4 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.37 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.37 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.36 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.39 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.39 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.43 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.37 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.38 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.31 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.33 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.33 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.32 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.29 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.32 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.24 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.27 |
rpoC | 764705 | p.Leu446Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781745 | c.186G>A | synonymous_variant | 0.12 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.17 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.2 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.26 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.21 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.27 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.27 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.27 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.25 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471845 | n.-1G>T | upstream_gene_variant | 0.14 |
rrs | 1471853 | n.8T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472958 | n.1113A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472988 | n.1143T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.1 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.1 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.11 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.17 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.16 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.11 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.1 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.19 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.26 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.27 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.27 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.17 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.17 |
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 | 0.18 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.16 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.16 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.16 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.13 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.14 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.14 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155206 | c.906C>T | synonymous_variant | 0.11 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448322 | c.-182G>A | upstream_gene_variant | 1.0 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.12 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.11 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.11 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.11 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.11 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.11 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.14 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.16 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |