Run ID: ERR4816093
Sample name:
Date: 01-04-2023 14:14:09
Number of reads: 1591038
Percentage reads mapped: 72.94
Strain: lineage1.1.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576675 | p.Arg443His | missense_variant | 1.0 |
rpoB | 759886 | p.Pro27His | missense_variant | 1.0 |
rpoB | 761605 | p.Leu600Pro | missense_variant | 0.11 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.16 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.12 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.11 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.12 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.12 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.12 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.14 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.13 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.15 |
rpoB | 762104 | c.2298C>T | synonymous_variant | 0.16 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.17 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.13 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.14 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.17 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.17 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.17 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.18 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.18 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.28 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.42 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.28 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.26 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.28 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.29 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.11 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.14 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.15 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
rpoC | 767308 | c.3939C>T | synonymous_variant | 1.0 |
mmpL5 | 775619 | c.2862G>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778099 | p.Asp128Asn | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.1 |
rplC | 801375 | c.567C>T | synonymous_variant | 1.0 |
Rv1258c | 1407190 | c.123_150delTGGGCAGGCCTCGATCGTGGCCAGTGCG | frameshift_variant | 1.0 |
embR | 1416574 | c.774A>G | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471886 | n.41G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>G | 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.842_843insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1474205 | n.548T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475692 | n.2035G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475715 | n.2058G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.27 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.3 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.29 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.28 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.27 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.36 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.44 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.39 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.3 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.28 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.3 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.24 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.24 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.21 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167970 | c.2643C>A | synonymous_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747022 | p.Val193Ile | missense_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086767 | c.-53A>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4038841 | p.Val622Leu | missense_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243056 | p.Pro1065Leu | missense_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245314 | c.2082G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408252 | c.-50A>G | upstream_gene_variant | 1.0 |
gid | 4408338 | c.-136A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1407190 | c.122_150delNNNNNNNNNNNNNNNNNNNNNNNNNNNNA | frameshift_variant | 1.0 |