Run ID: SRR8692791
Sample name:
Date: 13-08-2023 21:51:36
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 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.88 | linezolid |
embB | 4247582 | p.Ala357Ser | missense_variant | 0.15 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5161 | c.-79C>A | upstream_gene_variant | 0.18 |
gyrB | 6057 | p.Ser273Ile | missense_variant | 0.13 |
gyrB | 6661 | p.Met474Ile | missense_variant | 0.18 |
gyrB | 6914 | p.Gly559Arg | missense_variant | 0.17 |
gyrB | 7079 | p.Gly614Cys | missense_variant | 0.2 |
gyrA | 8135 | c.834C>A | synonymous_variant | 0.22 |
gyrA | 8174 | c.873C>A | synonymous_variant | 0.25 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.14 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.16 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.14 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.13 |
gyrA | 9248 | c.1947G>C | synonymous_variant | 0.15 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.15 |
gyrA | 9266 | p.Asp655Glu | missense_variant | 0.15 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.15 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.15 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.17 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.17 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.17 |
gyrA | 9324 | c.2023_2025delTCGinsAGC | synonymous_variant | 0.17 |
gyrA | 9335 | c.2034G>T | synonymous_variant | 0.16 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.16 |
gyrA | 9356 | c.2055G>C | synonymous_variant | 0.15 |
gyrA | 9653 | c.2352C>A | synonymous_variant | 0.18 |
fgd1 | 491083 | p.Val101Phe | missense_variant | 0.15 |
fgd1 | 491568 | c.786C>A | synonymous_variant | 0.14 |
fgd1 | 491580 | c.798C>A | synonymous_variant | 0.15 |
fgd1 | 491595 | c.813C>A | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.2 |
mshA | 576010 | c.663C>A | synonymous_variant | 0.25 |
mshA | 576066 | p.Pro240His | missense_variant | 0.15 |
rpoB | 759883 | p.Val26Ala | missense_variant | 0.2 |
rpoB | 759978 | p.Leu58Met | missense_variant | 0.17 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.18 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.18 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.25 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.25 |
rpoB | 760772 | c.966C>T | synonymous_variant | 0.17 |
rpoB | 761388 | p.Asp528Asn | missense_variant | 0.22 |
rpoB | 761445 | p.Arg547Ser | missense_variant | 0.14 |
rpoC | 762476 | c.-894C>A | upstream_gene_variant | 0.12 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.22 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.25 |
rpoB | 763125 | p.Pro1107Thr | missense_variant | 0.17 |
rpoB | 763132 | p.Pro1109Gln | missense_variant | 0.18 |
rpoC | 763262 | c.-108C>A | upstream_gene_variant | 0.15 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.1 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.1 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.13 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.14 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.15 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.15 |
rpoC | 763841 | p.Glu158* | stop_gained | 0.12 |
rpoC | 764213 | c.844C>A | synonymous_variant | 0.25 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.18 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.18 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.18 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.22 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.22 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.33 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.33 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.21 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.25 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.25 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.17 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.17 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.14 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.15 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.17 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.18 |
rpoC | 765423 | p.Asn685Thr | missense_variant | 0.15 |
rpoC | 765505 | c.2136C>T | synonymous_variant | 0.14 |
rpoC | 765839 | p.Val824Leu | missense_variant | 0.22 |
rpoC | 765847 | p.Asn826Lys | missense_variant | 0.2 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.18 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.17 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.18 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.18 |
rpoC | 766021 | c.2652G>T | synonymous_variant | 0.15 |
rpoC | 767076 | p.Ala1236Val | missense_variant | 0.13 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.18 |
mmpL5 | 776383 | p.Asp700Asn | missense_variant | 0.22 |
mmpL5 | 776402 | c.2079C>A | synonymous_variant | 0.22 |
mmpL5 | 776410 | p.Leu691Met | missense_variant | 0.2 |
mmpL5 | 776435 | c.2046T>C | synonymous_variant | 0.2 |
mmpL5 | 776832 | p.Thr550Ile | missense_variant | 0.22 |
mmpL5 | 777104 | c.1377G>T | synonymous_variant | 0.15 |
mmpL5 | 778648 | c.-168G>T | upstream_gene_variant | 0.25 |
mmpR5 | 779455 | p.Arg156* | stop_gained | 0.14 |
rpsL | 781651 | p.Arg31Leu | missense_variant | 0.15 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.11 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.11 |
rpsL | 781735 | p.Ser59Thr | missense_variant | 0.12 |
rpsL | 781737 | p.Gln60Gly | missense_variant | 0.12 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.12 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.12 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.21 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.21 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.17 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.17 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.17 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.21 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.18 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.18 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.14 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.14 |
fbiC | 1303145 | p.Ser72* | stop_gained | 0.15 |
fbiC | 1303168 | p.Gly80Cys | missense_variant | 0.15 |
fbiC | 1303833 | c.903C>A | synonymous_variant | 0.17 |
fbiC | 1305070 | p.Asp714Tyr | missense_variant | 0.2 |
Rv1258c | 1406435 | c.906G>T | synonymous_variant | 0.29 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.86 |
Rv1258c | 1406803 | p.Ala180Thr | missense_variant | 0.29 |
Rv1258c | 1407232 | p.Arg37Ser | missense_variant | 0.18 |
embR | 1416682 | c.666C>T | synonymous_variant | 0.17 |
embR | 1417191 | p.Asp53Tyr | missense_variant | 0.33 |
embR | 1417285 | p.Met21Ile | missense_variant | 0.2 |
atpE | 1461066 | p.Gly8Cys | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471755 | n.-91C>A | upstream_gene_variant | 0.15 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472825 | n.980G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473348 | n.1503C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474114 | n.457C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474457 | n.800C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474957 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475047 | n.1390G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.3 |
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 | 0.36 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673323 | c.-117C>A | upstream_gene_variant | 0.18 |
fabG1 | 1673714 | p.Ser92Tyr | missense_variant | 0.15 |
fabG1 | 1674041 | p.Gly201Ala | missense_variant | 0.11 |
inhA | 1674492 | p.Phe97Leu | missense_variant | 0.14 |
inhA | 1674558 | c.357C>A | synonymous_variant | 0.17 |
inhA | 1674894 | p.Asn231Lys | missense_variant | 0.15 |
rpsA | 1833556 | c.15C>A | synonymous_variant | 0.17 |
rpsA | 1833627 | p.Thr29Met | missense_variant | 0.12 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.12 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.12 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.14 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.14 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.13 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.12 |
rpsA | 1833727 | c.186G>A | synonymous_variant | 0.14 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.14 |
rpsA | 1833740 | p.Glu67* | stop_gained | 0.27 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.13 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.22 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.21 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.21 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.19 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.19 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.22 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.11 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.33 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.33 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.33 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.33 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.4 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.33 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.29 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.29 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
tlyA | 1918576 | p.Arg213Trp | missense_variant | 0.18 |
ndh | 2102863 | c.180C>T | synonymous_variant | 0.22 |
ndh | 2103202 | c.-160C>A | upstream_gene_variant | 0.4 |
katG | 2154255 | c.1857C>T | synonymous_variant | 0.17 |
katG | 2154938 | p.Arg392Trp | missense_variant | 0.15 |
katG | 2154989 | p.Pro375Ser | missense_variant | 0.17 |
katG | 2155104 | c.1008G>T | synonymous_variant | 0.13 |
katG | 2155493 | p.Asp207Tyr | missense_variant | 0.22 |
katG | 2155550 | p.Val188Ile | missense_variant | 0.14 |
katG | 2155917 | c.195C>G | synonymous_variant | 0.12 |
katG | 2156292 | c.-181G>T | upstream_gene_variant | 0.29 |
PPE35 | 2168055 | p.Pro853Gln | missense_variant | 0.14 |
PPE35 | 2168403 | p.Pro737Gln | missense_variant | 0.17 |
PPE35 | 2168777 | c.1836C>A | synonymous_variant | 0.13 |
PPE35 | 2168898 | p.Ala572Asp | missense_variant | 0.22 |
PPE35 | 2169284 | p.Tyr443* | stop_gained | 0.29 |
PPE35 | 2169317 | p.Phe432Leu | missense_variant | 0.22 |
Rv1979c | 2222845 | p.Gly107Val | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.18 |
pncA | 2289399 | c.-158C>A | upstream_gene_variant | 0.18 |
pncA | 2289715 | c.-474C>A | upstream_gene_variant | 0.33 |
pncA | 2290056 | c.-815C>A | upstream_gene_variant | 0.2 |
kasA | 2519349 | p.Ala412Val | missense_variant | 0.18 |
eis | 2714759 | p.Arg192Ser | missense_variant | 0.29 |
eis | 2715268 | p.Ala22Asp | missense_variant | 0.18 |
eis | 2715292 | p.Pro14Leu | missense_variant | 0.18 |
folC | 2746178 | p.Thr474Asn | missense_variant | 0.17 |
folC | 2746648 | c.951G>T | synonymous_variant | 0.14 |
pepQ | 2859906 | p.Gln171His | missense_variant | 0.13 |
Rv2752c | 3064588 | p.Arg535His | missense_variant | 0.2 |
Rv2752c | 3064764 | c.1428C>A | synonymous_variant | 0.17 |
Rv2752c | 3064802 | p.Glu464Lys | missense_variant | 0.17 |
Rv2752c | 3065521 | p.Arg224Leu | missense_variant | 0.13 |
thyA | 3074113 | p.Arg120Leu | missense_variant | 0.13 |
ald | 3086934 | p.Ala39Thr | missense_variant | 0.15 |
ald | 3087571 | p.Ser251* | stop_gained | 0.25 |
Rv3083 | 3448655 | p.Pro51Gln | missense_variant | 0.25 |
Rv3083 | 3449867 | p.Gly455Val | missense_variant | 0.13 |
fprA | 3474323 | p.Ala106Glu | missense_variant | 0.22 |
fprA | 3475191 | p.Cys395* | stop_gained | 0.17 |
whiB7 | 3568683 | c.-4G>C | upstream_gene_variant | 0.29 |
whiB7 | 3568859 | c.-180G>T | upstream_gene_variant | 0.15 |
fbiA | 3640387 | c.-156G>T | upstream_gene_variant | 0.18 |
fbiA | 3640685 | p.Gly48Val | missense_variant | 0.14 |
fbiA | 3641077 | p.Gln179Lys | missense_variant | 0.29 |
fbiB | 3641609 | c.75C>T | synonymous_variant | 0.2 |
fbiB | 3641769 | p.Glu79* | stop_gained | 0.15 |
fbiB | 3642787 | p.Trp418Leu | missense_variant | 0.17 |
alr | 3840398 | c.1023C>A | synonymous_variant | 0.13 |
alr | 3840883 | p.Arg180Cys | missense_variant | 0.22 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 0.14 |
rpoA | 3877569 | p.Pro313Ala | missense_variant | 0.13 |
rpoA | 3877584 | c.924C>G | synonymous_variant | 0.12 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.13 |
rpoA | 3877593 | p.Gly305Cys | missense_variant | 0.12 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.16 |
rpoA | 3877638 | c.870T>G | synonymous_variant | 0.13 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.17 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.13 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.13 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.13 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.15 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.15 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.15 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.16 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.16 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.11 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.11 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.11 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.11 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.11 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.12 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.12 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.13 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 0.17 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.11 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.11 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.1 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.1 |
rpoA | 3878384 | p.Leu42Met | missense_variant | 0.15 |
clpC1 | 4038301 | p.Val802Phe | missense_variant | 0.13 |
clpC1 | 4038674 | c.2031C>T | synonymous_variant | 0.12 |
clpC1 | 4039039 | p.Gly556Cys | missense_variant | 0.18 |
clpC1 | 4039157 | p.Lys516Asn | missense_variant | 0.17 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.1 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.11 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.13 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.13 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.14 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.15 |
clpC1 | 4039686 | p.Arg340His | missense_variant | 0.12 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.2 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.17 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.17 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.15 |
clpC1 | 4039978 | p.Lys243Glu | missense_variant | 0.12 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.12 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.13 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.13 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.13 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.13 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.13 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.13 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.18 |
clpC1 | 4040562 | p.Ser48* | stop_gained | 0.22 |
clpC1 | 4040715 | c.-11G>T | upstream_gene_variant | 0.4 |
clpC1 | 4040895 | c.-191C>T | upstream_gene_variant | 0.14 |
panD | 4044241 | p.Thr14Met | missense_variant | 0.14 |
embC | 4240181 | p.Ser107Pro | missense_variant | 0.12 |
embC | 4240745 | p.Gly295Cys | missense_variant | 0.29 |
embC | 4240964 | p.Gly368Arg | missense_variant | 0.13 |
embC | 4241168 | p.Leu436Met | missense_variant | 0.12 |
embC | 4242113 | p.Leu751Met | missense_variant | 0.12 |
embA | 4243307 | c.75G>T | synonymous_variant | 0.14 |
embB | 4249042 | c.2529G>A | synonymous_variant | 0.13 |
embB | 4249366 | p.Glu951Asp | missense_variant | 0.14 |
aftB | 4267622 | c.1215G>T | synonymous_variant | 0.13 |
aftB | 4268615 | c.222C>T | synonymous_variant | 0.13 |
ubiA | 4269580 | p.Pro85His | missense_variant | 0.18 |
ubiA | 4269585 | p.Glu83Asp | missense_variant | 0.17 |
ubiA | 4269634 | p.Ser67Leu | missense_variant | 0.33 |
ethA | 4326046 | p.Glu476Asp | missense_variant | 0.29 |
ethA | 4326547 | p.Lys309Asn | missense_variant | 0.2 |
ethA | 4326740 | p.Arg245His | missense_variant | 0.14 |
ethR | 4326922 | c.-627G>A | upstream_gene_variant | 0.2 |
ethR | 4327018 | c.-531G>T | upstream_gene_variant | 0.15 |
ethR | 4327072 | c.-477G>T | upstream_gene_variant | 0.15 |
ethR | 4327444 | c.-105C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338343 | p.Trp60* | stop_gained | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.17 |