Run ID: SRR8692807
Sample name:
Date: 13-08-2023 19:18:50
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 1.0 | linezolid |
pncA | 2288784 | p.Thr153Asn | missense_variant | 0.15 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5059 | c.-181G>T | upstream_gene_variant | 0.2 |
gyrB | 5080 | c.-160G>T | upstream_gene_variant | 0.2 |
gyrB | 5236 | c.-4G>T | upstream_gene_variant | 0.2 |
gyrB | 5270 | p.Glu11* | stop_gained | 0.18 |
gyrB | 5954 | p.Glu239Lys | missense_variant | 0.18 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.15 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.2 |
gyrB | 6202 | c.963C>G | synonymous_variant | 0.2 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.2 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.17 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.17 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.18 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.17 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.18 |
gyrB | 6713 | p.Arg492Ser | missense_variant | 0.17 |
gyrA | 7560 | p.His87Asn | missense_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.21 |
gyrA | 7657 | p.Pro119Gln | missense_variant | 0.19 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.33 |
gyrA | 8096 | c.795T>G | synonymous_variant | 0.4 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.4 |
gyrA | 8106 | p.Leu269Ile | missense_variant | 0.29 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.22 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.2 |
gyrA | 8270 | c.969G>T | synonymous_variant | 0.14 |
gyrA | 8285 | c.984C>T | synonymous_variant | 0.17 |
fgd1 | 491685 | c.903G>T | synonymous_variant | 0.17 |
ccsA | 620427 | c.537C>A | synonymous_variant | 0.17 |
ccsA | 620580 | p.Tyr230* | stop_gained | 0.13 |
rpoB | 759988 | p.Ser61* | stop_gained | 0.17 |
rpoB | 760018 | p.Arg71Leu | missense_variant | 0.18 |
rpoB | 760082 | c.276C>T | synonymous_variant | 0.15 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.17 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.17 |
rpoB | 760104 | c.298_300delTCGinsAGC | synonymous_variant | 0.17 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.17 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.17 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.17 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.18 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.2 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.2 |
rpoB | 760145 | c.339C>G | synonymous_variant | 0.2 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.25 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.25 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.25 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.23 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.25 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.23 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.29 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.29 |
rpoB | 760535 | c.729C>G | synonymous_variant | 0.29 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.31 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.27 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.33 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.33 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.33 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.33 |
rpoB | 760601 | c.795C>T | synonymous_variant | 0.27 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.22 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.21 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.17 |
rpoC | 762647 | c.-723G>T | upstream_gene_variant | 0.18 |
rpoB | 763311 | p.Glu1169* | stop_gained | 0.33 |
rpoC | 763357 | c.-13G>T | upstream_gene_variant | 0.29 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.13 |
rpoC | 763718 | p.Leu117Met | missense_variant | 0.14 |
rpoC | 764084 | p.Asn239Asp | missense_variant | 0.11 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.11 |
rpoC | 764126 | p.Thr253Ala | missense_variant | 0.11 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.11 |
rpoC | 764143 | c.774G>C | synonymous_variant | 0.11 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.13 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.13 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.12 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.11 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.11 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.11 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.19 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.24 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.24 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.24 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.17 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.17 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.17 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.17 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.2 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.19 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.17 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.18 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.16 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.14 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.15 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.15 |
rpoC | 765778 | c.2409C>G | synonymous_variant | 0.17 |
rpoC | 765779 | p.Asp804Lys | missense_variant | 0.17 |
rpoC | 765800 | p.Phe811Leu | missense_variant | 0.15 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.14 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.13 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.13 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.13 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.14 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.2 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.2 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.21 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.21 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.21 |
rpoC | 766525 | c.3156G>T | synonymous_variant | 0.13 |
rpoC | 766579 | c.3210C>T | synonymous_variant | 0.2 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.17 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.15 |
rpoC | 766711 | c.3342C>T | synonymous_variant | 0.14 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.14 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.14 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.15 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.14 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.17 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.2 |
rpoC | 766771 | c.3402G>C | synonymous_variant | 0.13 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.13 |
rpoC | 766775 | p.Arg1136Lys | missense_variant | 0.13 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.17 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
rpoC | 767011 | c.3642G>A | synonymous_variant | 0.12 |
mmpL5 | 776202 | p.Gly760Val | missense_variant | 0.12 |
mmpL5 | 776445 | p.Ala679Asp | missense_variant | 0.33 |
mmpL5 | 776806 | p.Gly559Trp | missense_variant | 0.2 |
mmpL5 | 777001 | p.His494Tyr | missense_variant | 0.25 |
mmpS5 | 778837 | p.Phe23Leu | missense_variant | 0.25 |
mmpL5 | 778852 | c.-372C>A | upstream_gene_variant | 0.25 |
mmpL5 | 779275 | c.-795G>T | upstream_gene_variant | 0.12 |
mmpL5 | 779316 | c.-836C>T | upstream_gene_variant | 0.12 |
rpsL | 781552 | c.-8G>T | upstream_gene_variant | 0.12 |
rpsL | 781616 | c.57C>A | synonymous_variant | 0.22 |
rpsL | 781748 | c.189C>A | synonymous_variant | 0.12 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.2 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.25 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.29 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.4 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.5 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.33 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.2 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.2 |
fbiC | 1303226 | p.Arg99Leu | missense_variant | 0.15 |
fbiC | 1304976 | p.Lys682Asn | missense_variant | 0.17 |
fbiC | 1305250 | c.2320C>A | synonymous_variant | 0.15 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471717 | n.-129G>T | upstream_gene_variant | 0.29 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472179 | n.334C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472303 | n.458G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472723 | n.878G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473162 | n.1317C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475176 | n.1519G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475257 | n.1600C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475993 | n.2336C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476415 | n.2758C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1833616 | c.75A>G | synonymous_variant | 0.12 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.12 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.11 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.11 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.24 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.22 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.22 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.24 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.25 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.25 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.25 |
rpsA | 1833727 | c.186G>A | synonymous_variant | 0.2 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.24 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.17 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.13 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.13 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.12 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.14 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.18 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.17 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.15 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.2 |
rpsA | 1834135 | c.594G>T | synonymous_variant | 0.17 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.2 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.2 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.27 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.2 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.2 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.18 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.15 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.15 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.15 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.16 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.14 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.14 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.14 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.15 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.15 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.18 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.19 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.3 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.3 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.12 |
ndh | 2102154 | p.Leu297Phe | missense_variant | 0.12 |
ndh | 2102790 | p.Leu85Met | missense_variant | 0.12 |
katG | 2153945 | p.Asp723Tyr | missense_variant | 0.17 |
katG | 2154426 | p.Asn562Lys | missense_variant | 0.12 |
katG | 2155473 | p.Lys213Asn | missense_variant | 0.12 |
katG | 2155495 | p.Gly206Val | missense_variant | 0.12 |
katG | 2155658 | p.Lys152Glu | missense_variant | 0.11 |
katG | 2155956 | c.156G>T | synonymous_variant | 0.12 |
katG | 2156069 | p.Ala15Ser | missense_variant | 0.12 |
katG | 2156074 | p.Thr13Asn | missense_variant | 0.12 |
PPE35 | 2167661 | p.Ser984Arg | missense_variant | 0.2 |
PPE35 | 2168176 | p.Gln813Lys | missense_variant | 0.12 |
PPE35 | 2168684 | c.1929C>A | synonymous_variant | 0.17 |
PPE35 | 2169135 | p.Pro493Gln | missense_variant | 0.18 |
PPE35 | 2170633 | c.-21C>A | upstream_gene_variant | 0.15 |
PPE35 | 2170691 | c.-79C>A | upstream_gene_variant | 0.18 |
Rv1979c | 2221806 | c.1359G>A | synonymous_variant | 0.25 |
Rv1979c | 2221872 | c.1293C>A | synonymous_variant | 0.33 |
Rv1979c | 2222049 | c.1116G>T | synonymous_variant | 0.15 |
Rv1979c | 2223097 | p.Gly23Val | missense_variant | 0.25 |
Rv1979c | 2223102 | p.Met21Ile | missense_variant | 0.25 |
Rv1979c | 2223199 | c.-35C>A | upstream_gene_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.22 |
pncA | 2289476 | c.-235G>T | upstream_gene_variant | 0.15 |
folC | 2747224 | c.375G>T | synonymous_variant | 0.12 |
pepQ | 2859393 | p.Leu342Phe | missense_variant | 0.22 |
pepQ | 2859404 | p.Glu339* | stop_gained | 0.22 |
pepQ | 2859438 | c.981T>C | synonymous_variant | 0.17 |
pepQ | 2859453 | c.966G>T | synonymous_variant | 0.17 |
pepQ | 2859465 | c.954G>T | synonymous_variant | 0.18 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.11 |
Rv2752c | 3065076 | c.1116T>G | synonymous_variant | 0.11 |
Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 0.12 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.12 |
Rv2752c | 3065097 | c.1095C>T | synonymous_variant | 0.12 |
Rv2752c | 3065106 | c.1086C>G | synonymous_variant | 0.14 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGG | synonymous_variant | 0.14 |
Rv2752c | 3065120 | p.Ile358Val | missense_variant | 0.13 |
Rv2752c | 3065130 | c.1062A>G | synonymous_variant | 0.12 |
Rv2752c | 3065133 | c.1059T>C | synonymous_variant | 0.12 |
Rv2752c | 3065142 | c.1050A>G | synonymous_variant | 0.12 |
Rv2752c | 3065697 | p.Ile165Val | missense_variant | 0.12 |
Rv2752c | 3065700 | c.492C>G | synonymous_variant | 0.13 |
Rv2752c | 3065703 | c.489A>G | synonymous_variant | 0.12 |
Rv2752c | 3065717 | p.Tyr159His | missense_variant | 0.12 |
Rv2752c | 3065727 | c.465C>G | synonymous_variant | 0.13 |
Rv2752c | 3065732 | c.460T>C | synonymous_variant | 0.13 |
Rv2752c | 3065742 | p.Thr150Ile | missense_variant | 0.14 |
Rv2752c | 3065745 | c.447C>G | synonymous_variant | 0.15 |
Rv2752c | 3065748 | c.444T>C | synonymous_variant | 0.16 |
Rv2752c | 3065757 | c.435C>G | synonymous_variant | 0.18 |
Rv2752c | 3065769 | c.423C>T | synonymous_variant | 0.18 |
Rv2752c | 3065775 | c.417T>C | synonymous_variant | 0.18 |
Rv2752c | 3065781 | c.411C>G | synonymous_variant | 0.18 |
Rv2752c | 3065785 | c.404_406delGGC | disruptive_inframe_deletion | 0.18 |
thyX | 3067502 | c.444C>A | synonymous_variant | 0.12 |
thyA | 3074193 | c.279C>A | synonymous_variant | 0.15 |
ald | 3086819 | c.-1C>A | upstream_gene_variant | 0.33 |
ald | 3086868 | p.Ala17Thr | missense_variant | 0.25 |
ald | 3086948 | c.129G>T | synonymous_variant | 0.25 |
ald | 3087390 | p.Gly191Cys | missense_variant | 0.14 |
ald | 3087444 | p.Ala209Ser | missense_variant | 0.14 |
ald | 3087483 | p.Ala222Ser | missense_variant | 0.14 |
ald | 3087539 | c.720G>T | synonymous_variant | 0.17 |
Rv3083 | 3449688 | p.Trp395Cys | missense_variant | 0.12 |
fprA | 3474376 | p.Ala124Ser | missense_variant | 0.17 |
fbiA | 3640362 | c.-181C>T | upstream_gene_variant | 0.13 |
fbiA | 3640397 | c.-146G>T | upstream_gene_variant | 0.12 |
fbiA | 3640429 | c.-114C>A | upstream_gene_variant | 0.15 |
fbiB | 3641034 | c.-501C>A | upstream_gene_variant | 0.14 |
fbiB | 3642107 | p.Glu191Asp | missense_variant | 0.14 |
alr | 3840231 | p.Arg397Leu | missense_variant | 0.13 |
alr | 3840511 | p.Asp304Tyr | missense_variant | 0.14 |
alr | 3840520 | p.Ala301Ser | missense_variant | 0.13 |
alr | 3840596 | p.Met275Ile | missense_variant | 0.2 |
alr | 3840637 | p.Pro262Thr | missense_variant | 0.15 |
alr | 3841073 | c.348C>A | synonymous_variant | 0.14 |
rpoA | 3877584 | c.924C>A | synonymous_variant | 0.18 |
rpoA | 3877601 | p.Gln303Lys | missense_variant | 0.22 |
rpoA | 3878369 | p.Pro47Thr | missense_variant | 0.17 |
rpoA | 3878384 | p.Leu42Met | missense_variant | 0.18 |
rpoA | 3878398 | p.Ser37* | stop_gained | 0.22 |
ddn | 3987245 | p.Gln134His | missense_variant | 0.25 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.11 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.12 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.12 |
clpC1 | 4038620 | p.Gln695His | missense_variant | 0.12 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.12 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.17 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.17 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.17 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.15 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.15 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.15 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.19 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.26 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.26 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.2 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.2 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.2 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.2 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.25 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.25 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.2 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.19 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.2 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.2 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.21 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.15 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.1 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.2 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.2 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.19 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.15 |
clpC1 | 4039262 | c.1443C>T | synonymous_variant | 0.17 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.17 |
clpC1 | 4039277 | c.1428C>A | synonymous_variant | 0.17 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.15 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.17 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.17 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.17 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.17 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.17 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.17 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.15 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.17 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.15 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.15 |
clpC1 | 4040462 | c.243C>T | synonymous_variant | 0.14 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.14 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.13 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.15 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.11 |
panD | 4044060 | c.222C>A | synonymous_variant | 0.25 |
embA | 4243771 | p.Gly180Val | missense_variant | 0.12 |
embB | 4247454 | p.Gly314Val | missense_variant | 0.12 |
embB | 4248510 | p.Ile666Thr | missense_variant | 0.22 |
aftB | 4267393 | p.Pro482Thr | missense_variant | 0.17 |
aftB | 4267413 | p.Gly475Asp | missense_variant | 0.17 |
ethA | 4326307 | c.1167C>A | synonymous_variant | 0.29 |
ethA | 4326482 | p.Arg331Leu | missense_variant | 0.25 |
ethR | 4327843 | p.Arg99Ser | missense_variant | 0.12 |
whiB6 | 4338495 | c.27T>C | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.25 |
gid | 4408215 | c.-13G>A | upstream_gene_variant | 0.13 |