Run ID: SRR13861629
Sample name:
Date: 03-04-2023 09:36:46
Number of reads: 709083
Percentage reads mapped: 14.2
Strain: lineage4.9
Drug-resistance: RR-TB
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.17 | rifampicin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.39 | streptomycin |
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5149 | c.-91G>C | upstream_gene_variant | 1.0 |
gyrB | 7090 | p.Asp617Glu | missense_variant | 0.86 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.14 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.15 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.16 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.16 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.15 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.18 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.15 |
gyrA | 8436 | p.Tyr379Asn | missense_variant | 0.96 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.14 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.19 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.2 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.19 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.19 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.19 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.14 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.15 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.15 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.19 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.15 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.14 |
gyrA | 8951 | p.Lys550Asn | missense_variant | 0.17 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.18 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.18 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.21 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.2 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.2 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.2 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.19 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.14 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.14 |
gyrA | 9099 | c.1798T>C | synonymous_variant | 0.17 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.15 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.15 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.15 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.15 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.17 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.16 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.17 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.16 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.15 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.2 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.15 |
gyrA | 9374 | c.2073G>C | synonymous_variant | 0.14 |
gyrA | 9386 | c.2085T>C | synonymous_variant | 0.15 |
gyrA | 9395 | c.2094G>C | synonymous_variant | 0.19 |
fgd1 | 491701 | p.His307Asn | missense_variant | 1.0 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.15 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.13 |
ccsA | 619765 | c.-126G>A | upstream_gene_variant | 1.0 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.18 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.15 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.16 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.18 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.16 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.14 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.18 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.15 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.13 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.14 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.15 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.17 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.17 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.19 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.16 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.15 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.28 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.25 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.16 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.18 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.17 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.17 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.16 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.16 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.15 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.15 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.16 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.15 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.16 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.16 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.13 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.21 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.18 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.24 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.21 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.19 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.19 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.19 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.17 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.17 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.17 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.17 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.17 |
rpoC | 762380 | c.-990T>G | upstream_gene_variant | 0.16 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.17 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.17 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.17 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.13 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.17 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.23 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.21 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.17 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.16 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.17 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.14 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.16 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.16 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.16 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.15 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.15 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.15 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.16 |
rpoC | 763708 | c.339G>A | synonymous_variant | 0.16 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.16 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.15 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.15 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.16 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.15 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.15 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.16 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.16 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.15 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.22 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.22 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.23 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.23 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.23 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.22 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.23 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.23 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.19 |
rpoC | 763919 | c.550C>T | synonymous_variant | 0.21 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.18 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.2 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.18 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.17 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.17 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.19 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.18 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.17 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.17 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.16 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.22 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.15 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.15 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.19 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.16 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.17 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.21 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.17 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.16 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.21 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.17 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.17 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.17 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.15 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.15 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.15 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.16 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.18 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.18 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.17 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.23 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.15 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.15 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.15 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.15 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.19 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.16 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.15 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.12 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.15 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.14 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.15 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.12 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.14 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.14 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.15 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.18 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.17 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.16 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.17 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.17 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.15 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.24 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.25 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.13 |
mmpL5 | 775867 | p.Arg872Gly | missense_variant | 0.94 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.13 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.12 |
mmpL5 | 776710 | p.Cys591Ser | missense_variant | 1.0 |
mmpL5 | 777625 | p.Gln286Lys | missense_variant | 1.0 |
mmpS5 | 778811 | p.Phe32Ser | missense_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.13 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.24 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.17 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.17 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.2 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.22 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.24 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.24 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.29 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.27 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.28 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.32 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.21 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.15 |
rplC | 800939 | p.Arg44His | missense_variant | 0.14 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.14 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.14 |
rplC | 800970 | c.162T>C | synonymous_variant | 0.14 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.14 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.14 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.14 |
embR | 1416901 | c.447G>C | synonymous_variant | 1.0 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.13 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.13 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474466 | n.810delA | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475224 | n.1567T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476589 | n.2932G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674231 | c.30T>C | synonymous_variant | 0.17 |
inhA | 1674237 | c.36T>C | synonymous_variant | 0.17 |
inhA | 1674239 | p.Ser13Thr | missense_variant | 0.17 |
inhA | 1674243 | c.42A>G | synonymous_variant | 0.17 |
inhA | 1674279 | c.78A>C | synonymous_variant | 0.15 |
inhA | 1674280 | p.Arg27Lys | missense_variant | 0.15 |
inhA | 1674285 | c.84A>G | synonymous_variant | 0.15 |
inhA | 1674301 | c.102_103delCC | frameshift_variant | 0.18 |
inhA | 1674307 | c.106C>T | synonymous_variant | 0.18 |
inhA | 1674315 | c.114C>G | synonymous_variant | 0.17 |
inhA | 1674321 | c.120G>C | synonymous_variant | 0.17 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.17 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.17 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.17 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.17 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.2 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.17 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.16 |
ndh | 2102009 | p.Ser345Asn | missense_variant | 0.17 |
ndh | 2102020 | c.1023A>G | synonymous_variant | 0.14 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.14 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.14 |
ndh | 2102131 | p.Gln304Lys | missense_variant | 0.17 |
ndh | 2102140 | c.903C>G | synonymous_variant | 0.17 |
ndh | 2102149 | c.894C>T | synonymous_variant | 0.17 |
ndh | 2102158 | c.885T>C | synonymous_variant | 0.15 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.13 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.2 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.2 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.22 |
katG | 2155677 | c.435C>G | synonymous_variant | 0.17 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.17 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.16 |
katG | 2155695 | p.Ala139Val | missense_variant | 0.15 |
katG | 2155701 | c.411C>T | synonymous_variant | 0.15 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.15 |
PPE35 | 2170487 | c.126T>A | synonymous_variant | 0.95 |
Rv1979c | 2221853 | p.Phe438Ile | missense_variant | 1.0 |
kasA | 2518468 | c.354A>T | synonymous_variant | 0.19 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.16 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.17 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.17 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.17 |
kasA | 2518513 | c.399C>G | synonymous_variant | 0.17 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.16 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.15 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.19 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.19 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.19 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.2 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.2 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.2 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.2 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.17 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.15 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.16 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.17 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.18 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.14 |
ribD | 2987369 | c.531G>A | synonymous_variant | 1.0 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.15 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.17 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.17 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.2 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.17 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.17 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.17 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.17 |
thyX | 3067463 | c.483C>A | synonymous_variant | 0.14 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.14 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.15 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.14 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.14 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.13 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.13 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.13 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.14 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.13 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.13 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.13 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.14 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.13 |
thyA | 3073975 | p.Arg166Pro | missense_variant | 0.93 |
Rv3236c | 3612013 | c.1104A>T | synonymous_variant | 1.0 |
Rv3236c | 3612032 | p.Met362Arg | missense_variant | 1.0 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.12 |
fbiB | 3642710 | c.1176G>C | synonymous_variant | 0.16 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.14 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.14 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.13 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.14 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.15 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.15 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.15 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.22 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.21 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.16 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.16 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.15 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.17 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.17 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.21 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.21 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.22 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.23 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.19 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.19 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.22 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.19 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.2 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.21 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.25 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.29 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.29 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.31 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.28 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.28 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.28 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.25 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.25 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.25 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.25 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.21 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.21 |
clpC1 | 4038272 | p.Gly811Ser | missense_variant | 0.21 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.2 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.21 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.17 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.2 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.2 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.18 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.17 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.18 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.13 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.19 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.17 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.19 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.23 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.22 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.21 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.23 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.22 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.2 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.17 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.19 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.17 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.15 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.15 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.17 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.17 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.17 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.17 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.2 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.19 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.22 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.2 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.17 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.17 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.18 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.16 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.16 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.16 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.17 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.17 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.17 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.17 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.17 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.2 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.19 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.17 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.17 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.17 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.16 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.16 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.17 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.17 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.17 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.15 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.15 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.14 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.21 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.23 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.23 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.19 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.19 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.17 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.14 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.15 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.13 |
clpC1 | 4040092 | p.Ser205Thr | missense_variant | 0.14 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.14 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.13 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.13 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.13 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.15 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.16 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.16 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.17 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.2 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.14 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.14 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.15 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.19 |
embC | 4240425 | p.Arg188Pro | missense_variant | 1.0 |
embC | 4240477 | c.615C>A | synonymous_variant | 1.0 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.14 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.12 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.16 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.18 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.2 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.19 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.16 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.16 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.15 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.15 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.18 |
embA | 4244214 | p.Ala328Ser | missense_variant | 1.0 |
embA | 4244849 | c.1617C>G | synonymous_variant | 1.0 |
embB | 4247198 | p.Thr229Pro | missense_variant | 1.0 |
embB | 4247381 | p.Trp290Arg | missense_variant | 1.0 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.17 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.16 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.2 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.2 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.2 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.2 |
embB | 4247536 | c.1023C>G | synonymous_variant | 0.21 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.16 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.17 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.18 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.18 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.18 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.19 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.2 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.24 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.24 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.2 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.21 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.2 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.19 |
embB | 4248304 | c.1791G>T | synonymous_variant | 0.19 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.24 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.24 |
embB | 4248322 | c.1809G>C | synonymous_variant | 0.23 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.18 |
embB | 4248346 | c.1833G>C | synonymous_variant | 0.18 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.18 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.18 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.18 |
embB | 4248361 | c.1848A>G | synonymous_variant | 0.18 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.18 |
aftB | 4268115 | p.Leu241Arg | missense_variant | 1.0 |
aftB | 4268696 | c.141G>A | synonymous_variant | 1.0 |
ethA | 4326298 | c.1176G>A | synonymous_variant | 0.94 |
whiB6 | 4338567 | c.-46C>A | upstream_gene_variant | 1.0 |