Run ID: ERR037504
Sample name:
Date: 31-03-2023 08:34:14
Number of reads: 8338942
Percentage reads mapped: 64.94
Strain: lineage4.9.1
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 | 1.0 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.45 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.55 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.4 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.12 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.14 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.13 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.13 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.1 |
rpoB | 762249 | p.Leu815Val | missense_variant | 0.24 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.28 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.14 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.12 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.14 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.14 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.17 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.18 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.22 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.19 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.16 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.12 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.15 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.15 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.18 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.16 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.12 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.1 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.12 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.11 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.1 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.11 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.15 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.13 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.13 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.17 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.14 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.16 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.15 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.15 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.16 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.18 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.25 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.23 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764767 | c.1398G>A | synonymous_variant | 0.19 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800997 | p.Asn63Lys | missense_variant | 0.24 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472495 | n.650C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473343 | n.1498G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474249 | n.592G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474381 | n.724T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474869 | n.1212G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475515 | n.1858G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475996 | n.2339T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.3 |
rpsA | 1833823 | c.282G>A | synonymous_variant | 0.14 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.14 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.14 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.14 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.14 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 0.11 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.11 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.14 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.12 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.1 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.11 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.15 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.3 |
Rv1979c | 2223145 | p.Arg7Lys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.27 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.36 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.17 |
Rv2752c | 3064552 | p.Arg547Pro | missense_variant | 0.26 |
Rv2752c | 3067191 | c.-1000G>A | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.18 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.28 |
rpoA | 3878238 | p.Asp90Glu | missense_variant | 0.2 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.19 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.12 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.13 |
clpC1 | 4039727 | c.978C>T | synonymous_variant | 0.14 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.14 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.12 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.11 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.11 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.13 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.13 |
clpC1 | 4039931 | p.Gly258Val | missense_variant | 0.14 |
clpC1 | 4039934 | c.771G>A | synonymous_variant | 0.16 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.14 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.13 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.13 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.12 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.11 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.11 |
clpC1 | 4040282 | c.423G>C | synonymous_variant | 0.1 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.12 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.12 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.11 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.11 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.11 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.15 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.17 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.23 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.39 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.22 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.22 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.27 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |