Run ID: ERR4818787
Sample name:
Date: 01-04-2023 15:45:03
Number of reads: 562812
Percentage reads mapped: 59.33
Strain: lineage6
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.18 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.87 | streptomycin |
katG | 2154234 | c.1877delT | frameshift_variant | 0.18 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8493 | p.Leu398Phe | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491668 | p.Lys296Glu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619912 | c.23_24delTC | frameshift_variant | 0.15 |
rpoB | 760855 | p.Thr350Ile | missense_variant | 1.0 |
rpoB | 760969 | p.Ser388Leu | missense_variant | 1.0 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.14 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.13 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.18 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.18 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
rpoB | 761826 | p.His674Asp | missense_variant | 0.13 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.25 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.17 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.27 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.2 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.2 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.25 |
rpoB | 762248 | c.2442G>C | synonymous_variant | 0.25 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.25 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.2 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.3 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.33 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.33 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.33 |
rpoC | 763076 | c.-294C>T | upstream_gene_variant | 0.43 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.43 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.43 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.38 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.38 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.38 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.29 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.29 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.15 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.15 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.15 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.25 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.29 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.33 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.3 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.4 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.4 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.44 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.4 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.4 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.36 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.36 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.3 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.36 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.46 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.43 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.38 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.27 |
rpoC | 764291 | p.Ser308Pro | missense_variant | 0.18 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.18 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.18 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.18 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.18 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.2 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.29 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.22 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.25 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.25 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.38 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.38 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.43 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.43 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.25 |
rpoC | 764737 | c.1368G>T | synonymous_variant | 0.25 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.29 |
rpoC | 764910 | p.Pro514Leu | missense_variant | 0.25 |
rpoC | 766231 | c.2862T>C | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775994 | p.Ile829Met | missense_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778753 | c.-273C>T | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303018 | c.88C>T | synonymous_variant | 0.12 |
fbiC | 1304582 | p.Asn551Ser | missense_variant | 0.11 |
fbiC | 1304902 | p.Glu658Lys | missense_variant | 0.12 |
Rv1258c | 1406685 | p.Val219Ala | missense_variant | 1.0 |
embR | 1416633 | p.Leu239Val | missense_variant | 1.0 |
atpE | 1460909 | c.-136C>A | upstream_gene_variant | 0.4 |
atpE | 1461251 | c.207G>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
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 | 0.71 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.92 |
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 | 0.93 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.17 |
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 | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.4 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.4 |
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 | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475715 | n.2058G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.36 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.42 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.42 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.55 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.55 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.36 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.18 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.55 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.27 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.3 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.23 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.17 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.23 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.15 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1834028 | p.Pro163Ala | missense_variant | 0.12 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.31 |
rpsA | 1834213 | c.672G>A | synonymous_variant | 0.18 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.43 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.43 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.4 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.46 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.55 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.5 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.5 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918736 | p.Glu266Gly | missense_variant | 0.22 |
ndh | 2101956 | p.Gln363Lys | missense_variant | 0.17 |
katG | 2154066 | c.2046T>C | synonymous_variant | 0.4 |
katG | 2154604 | p.Val503Ala | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2155808 | p.Phe102Leu | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168463 | p.Pro717Leu | missense_variant | 0.22 |
PPE35 | 2168964 | p.Val550Ala | missense_variant | 0.2 |
PPE35 | 2169365 | p.Ser416Arg | missense_variant | 0.18 |
PPE35 | 2169453 | p.Tyr387Phe | missense_variant | 0.12 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.13 |
PPE35 | 2170709 | c.-97A>G | upstream_gene_variant | 0.18 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223120 | c.44dupG | frameshift_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223363 | c.-199A>G | upstream_gene_variant | 0.29 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519281 | c.1167G>T | synonymous_variant | 0.2 |
eis | 2714909 | p.Val142Leu | missense_variant | 0.12 |
folC | 2747045 | p.Asn185Ser | missense_variant | 0.17 |
thyX | 3067265 | c.681C>T | synonymous_variant | 0.22 |
thyX | 3067872 | c.73delT | frameshift_variant | 0.12 |
thyA | 3074221 | p.Ala84Gly | missense_variant | 0.17 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fbiD | 3339005 | c.-113_-112insA | upstream_gene_variant | 0.11 |
Rv3083 | 3448990 | p.Cys163Arg | missense_variant | 0.13 |
Rv3083 | 3449396 | p.Cys298Tyr | missense_variant | 1.0 |
fprA | 3473972 | c.-35T>C | upstream_gene_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612143 | p.Arg325His | missense_variant | 1.0 |
fbiB | 3642018 | p.Asp162His | missense_variant | 0.11 |
clpC1 | 4038587 | c.2118C>A | synonymous_variant | 0.25 |
clpC1 | 4039804 | p.Ala301Ser | missense_variant | 0.75 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.75 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.75 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.43 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.43 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.43 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.33 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.2 |
clpC1 | 4039910 | c.795C>T | synonymous_variant | 0.2 |
clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.13 |
panD | 4044432 | c.-151T>G | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241843 | p.Leu661Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244379 | p.Pro383Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247487 | p.Ser325Asn | missense_variant | 0.12 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248311 | p.Ala600Thr | missense_variant | 0.17 |
embB | 4248726 | p.Ser738Phe | missense_variant | 0.18 |
aftB | 4267103 | c.1734G>A | synonymous_variant | 0.25 |
aftB | 4267599 | p.Phe413Ser | missense_variant | 0.22 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269522 | c.-686C>T | upstream_gene_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
aftB | 4269693 | c.-857C>T | upstream_gene_variant | 1.0 |
ethA | 4326465 | p.Ile337Val | missense_variant | 1.0 |
ethA | 4327086 | p.Thr130Ala | missense_variant | 0.17 |
ethR | 4327246 | c.-303G>C | upstream_gene_variant | 0.12 |
ethR | 4327767 | c.220delA | frameshift_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407669 | p.Met178Ile | missense_variant | 0.29 |
gid | 4408034 | p.Glu57Lys | missense_variant | 1.0 |