Run ID: ERR2229198
Sample name:
Date: 31-03-2023 16:48:25
Number of reads: 731987
Percentage reads mapped: 35.37
Strain: lineage4.8
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761116 | p.Asn437Thr | missense_variant | 0.17 | rifampicin |
katG | 2155102 | p.Tyr337Phe | missense_variant | 0.19 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6666 | c.1429delG | frameshift_variant | 0.13 |
gyrB | 7139 | p.Arg634Cys | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9287 | c.1986G>A | synonymous_variant | 0.17 |
gyrA | 9505 | p.Thr735Ile | missense_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.36 |
ccsA | 620309 | p.Phe140Tyr | missense_variant | 0.17 |
ccsA | 620598 | c.708C>T | synonymous_variant | 0.18 |
rpoB | 760461 | p.Arg219Cys | missense_variant | 0.13 |
rpoB | 760916 | c.1110C>G | synonymous_variant | 0.29 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.38 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.31 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.31 |
rpoB | 760959 | p.Val385Leu | missense_variant | 0.31 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.33 |
rpoB | 760968 | p.Ser388Ala | missense_variant | 0.33 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.33 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.44 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.47 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.42 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.27 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.28 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.28 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.28 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.24 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.24 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.25 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.17 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761196 | c.1390_1391insA | frameshift_variant | 0.25 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.38 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.23 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.2 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.2 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.19 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.17 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.17 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.17 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 0.15 |
rpoB | 761289 | p.Ser495Ala | missense_variant | 0.15 |
rpoB | 761293 | p.Val496Ala | missense_variant | 0.16 |
rpoB | 761296 | p.Tyr497Phe | missense_variant | 0.15 |
rpoB | 761299 | p.Ala498Gly | missense_variant | 0.15 |
rpoB | 761322 | p.Ile506Val | missense_variant | 0.26 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.29 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.14 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.14 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.15 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.14 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.18 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.17 |
rpoB | 761613 | p.Ala603Ser | missense_variant | 0.17 |
rpoB | 761631 | p.Ala609Ser | missense_variant | 0.17 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.17 |
rpoB | 761643 | p.Val613Leu | missense_variant | 0.17 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.17 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.17 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.15 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.14 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 0.14 |
rpoB | 762003 | p.Asn733His | missense_variant | 0.13 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.12 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.12 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.12 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.13 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.13 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.13 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.13 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.13 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.19 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.18 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.2 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.25 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.24 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.3 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.33 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.28 |
rpoB | 762173 | p.Glu789Asp | missense_variant | 0.28 |
rpoB | 762175 | c.2369_2370insCG | frameshift_variant | 0.27 |
rpoB | 762178 | p.Arg791Pro | missense_variant | 0.27 |
rpoB | 762179 | c.2374_2375delGA | frameshift_variant | 0.27 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.29 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.29 |
rpoB | 762230 | c.2424G>C | synonymous_variant | 0.21 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.22 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.23 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.12 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.33 |
rpoC | 762398 | c.-972T>G | upstream_gene_variant | 0.33 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.18 |
rpoC | 762407 | c.-963G>C | upstream_gene_variant | 0.25 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.25 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.25 |
rpoB | 762426 | p.Ser874Thr | missense_variant | 0.4 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.22 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.25 |
rpoB | 762474 | p.Gly890Ser | missense_variant | 0.25 |
rpoB | 762480 | p.Ile892Val | missense_variant | 0.25 |
rpoC | 762485 | c.-885G>C | upstream_gene_variant | 0.25 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.22 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.13 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.18 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.24 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.23 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.29 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.21 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.15 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.17 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.19 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.21 |
rpoB | 763005 | p.Cys1067Gly | missense_variant | 0.21 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.13 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.15 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.27 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.5 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.57 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.33 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.15 |
rpoC | 763453 | c.84C>G | synonymous_variant | 0.34 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.37 |
rpoC | 763480 | c.111C>G | synonymous_variant | 0.48 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.5 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.48 |
rpoC | 763504 | c.135C>G | synonymous_variant | 0.49 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.51 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.45 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.47 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.47 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.54 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.39 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.39 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.46 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.45 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.5 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.48 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.5 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.36 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.31 |
rpoC | 763705 | c.336G>C | synonymous_variant | 0.31 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.32 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.32 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.32 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.33 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.23 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.23 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.25 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.12 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.14 |
rpoC | 764217 | p.Asn283Thr | missense_variant | 0.14 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.12 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.15 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.5 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.47 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.34 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.31 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.26 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.26 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.26 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.27 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.27 |
rpoC | 764449 | c.1080G>T | synonymous_variant | 0.27 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.27 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.31 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.31 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.22 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.24 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.33 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.46 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.58 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.61 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.61 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.55 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.45 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.45 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.34 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.26 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.36 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.4 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.33 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.29 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.24 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.28 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.2 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.21 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.17 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.21 |
rpoC | 765551 | p.Gly728Arg | missense_variant | 0.17 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.29 |
rpoC | 767056 | c.3687C>G | synonymous_variant | 0.29 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 0.25 |
rpoC | 767062 | c.3693C>G | synonymous_variant | 0.25 |
rpoC | 767068 | c.3699G>C | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776730 | p.Tyr584Phe | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.29 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.24 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.27 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.27 |
rplC | 800667 | c.-142_-141delTCinsAG | upstream_gene_variant | 0.14 |
fbiC | 1303464 | c.534A>G | synonymous_variant | 0.2 |
fbiC | 1303470 | c.540T>C | synonymous_variant | 0.2 |
fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406448 | p.Leu298Pro | missense_variant | 0.29 |
embR | 1416578 | p.Gln257Arg | missense_variant | 0.14 |
atpE | 1461228 | p.Ala62Thr | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472133 | n.288G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472309 | n.464C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472310 | n.465T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472446 | n.601T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472466 | n.621C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472492 | n.648_651delTACT | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472498 | n.656_657insTAGG | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472517 | n.672T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472545 | n.700A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472583 | n.738T>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472675 | n.832delC | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472791 | n.946G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473065 | n.1220C>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473289 | n.1444T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1473392 | n.-266C>A | upstream_gene_variant | 0.36 |
rrl | 1473679 | n.22_23insAC | non_coding_transcript_exon_variant | 0.41 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473722 | n.65G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474229 | n.572A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474235 | n.578_579insT | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474286 | n.629C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474309 | n.652G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474311 | n.654G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474830 | n.1173A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475028 | n.1371G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475068 | n.1411A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475078 | n.1421T>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475082 | n.1425C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475571 | n.1914A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475586 | n.1929C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475706 | n.2049A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475757 | n.2100_2101insG | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475769 | n.2112_2113insC | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475782 | n.2125T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475983 | n.2326T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475996 | n.2339T>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476000 | n.2343G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476046 | n.2389G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476060 | n.2403T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476088 | n.2431A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476095 | n.2439delT | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476099 | n.2442A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476103 | n.2446_2447insG | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476115 | n.2458T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476116 | n.2459A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476268 | n.2611A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476275 | n.2618T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476325 | n.2668A>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476531 | n.2874T>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
fabG1 | 1673416 | c.-24G>A | upstream_gene_variant | 0.14 |
fabG1 | 1673993 | p.Tyr185Cys | missense_variant | 0.18 |
inhA | 1674072 | c.-130C>T | upstream_gene_variant | 0.13 |
fabG1 | 1674118 | p.Glu227* | stop_gained | 0.14 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.15 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.21 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.32 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.35 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.38 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.29 |
rpsA | 1833782 | p.Ser81Thr | missense_variant | 0.29 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.42 |
rpsA | 1833794 | p.Glu85His | missense_variant | 0.42 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.31 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.26 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.26 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 0.25 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.33 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.35 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.36 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.33 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.36 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.32 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.23 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.19 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.2 |
rpsA | 1833904 | p.Glu121Asp | missense_variant | 0.19 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.2 |
rpsA | 1833910 | c.371_372delAG | frameshift_variant | 0.2 |
rpsA | 1833915 | c.374_375insAT | frameshift_variant | 0.2 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.22 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.25 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.22 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.27 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.21 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.18 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.29 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.25 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.25 |
rpsA | 1834028 | p.Pro163Thr | missense_variant | 0.14 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.29 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.29 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.14 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.25 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.18 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.19 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.31 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.37 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.38 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.36 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.39 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.4 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.38 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.38 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.41 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.45 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.42 |
rpsA | 1834345 | p.Asp268Glu | missense_variant | 0.34 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.35 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.32 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.31 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.31 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.31 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.37 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.44 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.52 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.5 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.33 |
rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.33 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.33 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.32 |
rpsA | 1834439 | p.Lys300Arg | missense_variant | 0.33 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.3 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.26 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.24 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.24 |
rpsA | 1834477 | c.936C>G | synonymous_variant | 0.22 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918584 | c.645A>G | synonymous_variant | 0.18 |
ndh | 2102565 | c.478C>A | synonymous_variant | 0.25 |
ndh | 2103198 | c.-156C>A | upstream_gene_variant | 0.12 |
katG | 2155104 | c.1008G>C | synonymous_variant | 0.19 |
katG | 2155375 | p.Val246Arg | missense_variant | 0.13 |
katG | 2155377 | c.735G>C | synonymous_variant | 0.12 |
katG | 2155389 | c.723C>G | synonymous_variant | 0.13 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.17 |
katG | 2155638 | p.Lys158Ser | missense_variant | 0.15 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.13 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.12 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.13 |
katG | 2155735 | p.Met126Gln | missense_variant | 0.13 |
katG | 2155741 | p.Gly124Ser | missense_variant | 0.14 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.14 |
katG | 2155747 | p.Ala122Gly | missense_variant | 0.14 |
katG | 2156181 | c.-70T>C | upstream_gene_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.73 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.29 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.38 |
PPE35 | 2170274 | p.Asn113Lys | missense_variant | 0.22 |
Rv1979c | 2222686 | p.Lys160Arg | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289702 | c.-461T>G | upstream_gene_variant | 0.22 |
pncA | 2289945 | c.-704T>C | upstream_gene_variant | 0.12 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.14 |
kasA | 2519079 | p.Glu322Gly | missense_variant | 0.27 |
eis | 2714329 | p.Asp335Val | missense_variant | 0.13 |
folC | 2747100 | p.Pro167Ser | missense_variant | 0.13 |
pepQ | 2860222 | p.Ser66Leu | missense_variant | 0.14 |
pepQ | 2860585 | c.-167G>C | upstream_gene_variant | 0.18 |
ribD | 2987506 | p.Leu223Gln | missense_variant | 0.22 |
Rv2752c | 3065257 | p.Met312Thr | missense_variant | 0.14 |
Rv2752c | 3065647 | p.Pro182Leu | missense_variant | 0.12 |
Rv2752c | 3066126 | c.65delG | frameshift_variant | 0.14 |
fbiD | 3339419 | p.Arg101Leu | missense_variant | 0.12 |
Rv3236c | 3612526 | c.591G>T | synonymous_variant | 0.2 |
alr | 3840245 | c.1176C>T | synonymous_variant | 0.18 |
rpoA | 3877776 | c.732T>A | synonymous_variant | 0.18 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.12 |
clpC1 | 4038721 | p.Leu662Met | missense_variant | 0.25 |
clpC1 | 4038743 | p.Thr654Val | missense_variant | 0.15 |
clpC1 | 4038746 | c.1959C>T | synonymous_variant | 0.19 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.19 |
clpC1 | 4038752 | c.1953G>A | synonymous_variant | 0.15 |
clpC1 | 4038755 | p.Gly650Ala | missense_variant | 0.38 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.36 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.36 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.32 |
clpC1 | 4038782 | p.Val641Ile | missense_variant | 0.32 |
clpC1 | 4038801 | p.Tyr635Phe | missense_variant | 0.42 |
clpC1 | 4038806 | p.Glu633Asp | missense_variant | 0.37 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.37 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.33 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.18 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.17 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.33 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.41 |
clpC1 | 4038896 | c.1809C>G | synonymous_variant | 0.3 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.2 |
clpC1 | 4039031 | c.1674T>G | synonymous_variant | 0.17 |
clpC1 | 4039061 | c.1644G>A | synonymous_variant | 0.12 |
clpC1 | 4039257 | p.Gln483Leu | missense_variant | 0.15 |
clpC1 | 4039266 | p.Asp480Thr | missense_variant | 0.15 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.29 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.33 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.29 |
clpC1 | 4039403 | p.Glu434Asp | missense_variant | 0.29 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.23 |
clpC1 | 4039412 | p.Ala431Val | missense_variant | 0.23 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.23 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.23 |
clpC1 | 4039434 | p.Phe424Tyr | missense_variant | 0.23 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.13 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.24 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.27 |
clpC1 | 4039457 | c.1248C>G | synonymous_variant | 0.27 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.25 |
clpC1 | 4039466 | c.1239T>G | synonymous_variant | 0.25 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.25 |
clpC1 | 4039481 | p.Ala408Ser | missense_variant | 0.25 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.25 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.29 |
clpC1 | 4039502 | c.1203C>T | synonymous_variant | 0.33 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.29 |
clpC1 | 4039523 | c.1182C>T | synonymous_variant | 0.12 |
clpC1 | 4039532 | p.Asn391Ser | missense_variant | 0.25 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.31 |
clpC1 | 4039544 | c.1161C>T | synonymous_variant | 0.25 |
clpC1 | 4039553 | p.Thr384Gln | missense_variant | 0.25 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.25 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.23 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.25 |
clpC1 | 4039574 | p.Ala377Ser | missense_variant | 0.25 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.21 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.32 |
clpC1 | 4039640 | c.1065C>G | synonymous_variant | 0.35 |
clpC1 | 4039647 | p.Glu353Ser | missense_variant | 0.3 |
clpC1 | 4039651 | p.Val352Leu | missense_variant | 0.29 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.27 |
clpC1 | 4039661 | p.Gly348Ala | missense_variant | 0.26 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.23 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.33 |
clpC1 | 4039685 | c.1020C>G | synonymous_variant | 0.33 |
clpC1 | 4039697 | c.1008C>T | synonymous_variant | 0.19 |
clpC1 | 4039708 | c.996_997insTG | frameshift_variant | 0.21 |
clpC1 | 4039712 | c.991_992delTA | frameshift_variant | 0.26 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 0.14 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.14 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.14 |
clpC1 | 4039789 | p.Ser306Thr | missense_variant | 0.12 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.12 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.23 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.14 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.16 |
clpC1 | 4039838 | c.867G>C | synonymous_variant | 0.33 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.28 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.28 |
clpC1 | 4039868 | c.837C>G | synonymous_variant | 0.28 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.33 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 0.44 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.48 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.43 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.42 |
clpC1 | 4039919 | c.786C>G | synonymous_variant | 0.42 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.3 |
clpC1 | 4039943 | p.Ser254Ala | missense_variant | 0.24 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.39 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.39 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.51 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.38 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.37 |
clpC1 | 4040009 | p.Ala232Lys | missense_variant | 0.37 |
clpC1 | 4040021 | c.684A>G | synonymous_variant | 0.52 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.52 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.52 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.52 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.53 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.5 |
clpC1 | 4040060 | p.Ile215Val | missense_variant | 0.48 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.5 |
clpC1 | 4040072 | c.633C>T | synonymous_variant | 0.49 |
clpC1 | 4040084 | c.621C>T | synonymous_variant | 0.47 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.47 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.47 |
clpC1 | 4040093 | c.610_612delCTCinsTTG | synonymous_variant | 0.47 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.52 |
clpC1 | 4040123 | p.Glu194Asp | missense_variant | 0.35 |
clpC1 | 4040126 | c.579C>G | synonymous_variant | 0.33 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.13 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.18 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.26 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.29 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.25 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.21 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.13 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.26 |
panD | 4044299 | c.-18A>T | upstream_gene_variant | 0.25 |
embC | 4240873 | c.1011C>A | synonymous_variant | 0.14 |
embC | 4241632 | p.Phe590Leu | missense_variant | 0.25 |
embC | 4241717 | p.Arg619Trp | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245539 | c.-975C>A | upstream_gene_variant | 0.2 |
embB | 4247956 | c.1443G>A | synonymous_variant | 0.2 |
embB | 4249370 | c.2857C>T | synonymous_variant | 0.13 |
aftB | 4267816 | p.Ala341Ser | missense_variant | 0.14 |
aftB | 4269108 | c.-272C>A | upstream_gene_variant | 0.15 |
ethA | 4326965 | p.Asp170Gly | missense_variant | 0.12 |
ethA | 4327088 | p.Leu129Pro | missense_variant | 0.13 |
ethR | 4327607 | p.Pro20Gln | missense_variant | 0.12 |
whiB6 | 4338392 | p.Thr44Ser | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |