Run ID: ERR4822104
Sample name:
Date: 01-04-2023 17:38:17
Number of reads: 290389
Percentage reads mapped: 35.75
Strain: lineage3
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.33 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.76 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491607 | c.825G>A | synonymous_variant | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575405 | p.Arg20Cys | missense_variant | 0.13 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.67 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.67 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.5 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.5 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.5 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.5 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.5 |
rpoB | 762300 | p.Lys832* | stop_gained | 0.33 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.4 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.5 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.4 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.33 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.25 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.33 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.5 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.71 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.71 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.29 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.71 |
rpoB | 763077 | p.Val1091Ser | missense_variant | 0.71 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.71 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.25 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.71 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.71 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.75 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.67 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.4 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.4 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.4 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.4 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.4 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.4 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 1.0 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.75 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.75 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.75 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.6 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.6 |
rpoC | 763555 | c.186C>T | synonymous_variant | 0.6 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.6 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.6 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.6 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.4 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.33 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.33 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.33 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.33 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.33 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.33 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.33 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.33 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.33 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.5 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.4 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.17 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.2 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.18 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.27 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.38 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.42 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.27 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.43 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.4 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.38 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.13 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.5 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.5 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.5 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.5 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.33 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.45 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.5 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.45 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.43 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779221 | p.Gly78Arg | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.25 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.29 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.29 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.29 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.29 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.29 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.29 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.29 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.29 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.33 |
fbiC | 1303147 | p.Ala73Thr | missense_variant | 0.5 |
fbiC | 1303868 | p.Asp313Gly | missense_variant | 0.25 |
Rv1258c | 1406935 | p.Gly136Ser | missense_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.67 |
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 | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.58 |
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 | 0.89 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473122 | n.1278A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 1.0 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
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 | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
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 | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.57 |
inhA | 1673450 | c.-752C>A | upstream_gene_variant | 0.25 |
rpsA | 1833897 | p.Leu119Pro | missense_variant | 0.5 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.22 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.22 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.22 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.22 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.25 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.5 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.44 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.71 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.67 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.67 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.67 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.5 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.4 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.27 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.27 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103206 | c.-164T>C | upstream_gene_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
Rv1979c | 2222758 | p.Val136Ala | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288700 | p.Glu181Trp | missense_variant | 0.29 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
kasA | 2519008 | c.894C>T | synonymous_variant | 0.17 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726208 | p.Ile6Val | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642126 | p.Ile198Val | missense_variant | 0.67 |
fbiB | 3642467 | c.933T>C | synonymous_variant | 0.2 |
embC | 4241456 | p.Ala532Thr | missense_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242946 | c.3086delG | frameshift_variant | 0.2 |
embB | 4246987 | c.474C>T | synonymous_variant | 0.14 |
aftB | 4267936 | p.Val301Leu | missense_variant | 0.29 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |