Run ID: ERR4817464
Sample name:
Date: 01-04-2023 15:00:22
Number of reads: 626718
Percentage reads mapped: 80.4
Strain: lineage3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.44 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.19 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.22 |
ccsA | 620271 | c.381C>G | synonymous_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.15 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 0.15 |
rpoB | 762003 | p.Asn733Arg | missense_variant | 0.14 |
rpoB | 762009 | p.Leu735Val | missense_variant | 0.15 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.12 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.12 |
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>A | synonymous_variant | 0.12 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.18 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.17 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.18 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.18 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.12 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.13 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.14 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.17 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.17 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.18 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.12 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.19 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.2 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.21 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.19 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.12 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.1 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.1 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.1 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.11 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.1 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.11 |
rpoC | 764380 | c.1011G>T | synonymous_variant | 0.14 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.1 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.11 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.1 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.1 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303781 | p.Phe284Ser | missense_variant | 0.1 |
fbiC | 1304649 | c.1719C>T | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472101 | n.256G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472583 | n.738T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473266 | n.1421A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.17 |
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 | 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 | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474672 | n.1015C>T | 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 | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475707 | n.2050T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475761 | n.2104C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475766 | n.2109_2110insTGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673973 | c.-229G>A | upstream_gene_variant | 0.14 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.11 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.1 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.14 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.18 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.18 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.18 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.15 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.15 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.15 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.16 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.11 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.11 |
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 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518319 | p.Asp69Asn | missense_variant | 0.14 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086997 | p.Thr60Gly | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878182 | p.Asp109Gly | missense_variant | 0.13 |
clpC1 | 4040679 | p.Ala9Asp | missense_variant | 0.12 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4241585 | c.1725delC | frameshift_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408345 | c.-143C>T | upstream_gene_variant | 1.0 |