Run ID: ERR3468613
Sample name:
Date: 01-04-2023 02:19:23
Number of reads: 786141
Percentage reads mapped: 67.89
Strain: La1.8.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761098 | p.Ser431Thr | missense_variant | 0.11 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.66 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.71 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.54 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7325 | c.24T>A | synonymous_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 8899 | p.Leu533Pro | missense_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.11 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.11 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.11 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.11 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.12 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.14 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.15 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.15 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.26 |
rpoC | 763573 | c.204G>A | synonymous_variant | 0.25 |
rpoC | 763600 | c.231C>G | synonymous_variant | 0.35 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.35 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.39 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.33 |
rpoC | 763624 | c.255C>A | synonymous_variant | 0.37 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.42 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.42 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.42 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.32 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.33 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.32 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.3 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.24 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.17 |
rpoC | 763705 | c.336G>C | synonymous_variant | 0.17 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.18 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.19 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.17 |
rpoC | 763720 | c.351G>T | synonymous_variant | 0.16 |
rpoC | 763723 | c.354G>T | synonymous_variant | 0.18 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>T | synonymous_variant | 0.17 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.17 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.16 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.12 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.18 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.16 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.17 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.14 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.12 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.12 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.12 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.12 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.12 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.12 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.16 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.17 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.19 |
rpoC | 764767 | c.1398G>A | synonymous_variant | 0.2 |
rpoC | 764779 | c.1410G>A | synonymous_variant | 0.17 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.19 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.14 |
rpoC | 764804 | p.Gln479Tyr | missense_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.14 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.15 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.16 |
rpoC | 764837 | p.Val490Ile | missense_variant | 0.15 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.17 |
rpoC | 764848 | c.1479G>A | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800630 | c.-179G>T | upstream_gene_variant | 0.14 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.14 |
rplC | 800639 | c.-170C>A | upstream_gene_variant | 0.14 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.14 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.13 |
rplC | 800668 | c.-141_-140delCGinsGC | upstream_gene_variant | 0.13 |
rplC | 800681 | c.-128C>T | upstream_gene_variant | 0.14 |
rplC | 800684 | c.-125G>A | upstream_gene_variant | 0.14 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.14 |
rplC | 800702 | c.-107G>T | upstream_gene_variant | 0.17 |
rplC | 800703 | c.-106_-104delTTGinsCTT | upstream_gene_variant | 0.17 |
rplC | 800729 | c.-80G>C | upstream_gene_variant | 0.14 |
rplC | 800733 | c.-76A>G | upstream_gene_variant | 0.14 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.13 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472495 | n.650C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474012 | n.355C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474286 | n.629C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474287 | n.630T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474296 | n.640_654delCTCCGGAGGAGGGTG | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474869 | n.1212G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475996 | n.2339T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476104 | n.2447T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476105 | n.2448G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.62 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.11 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154422 | p.Thr564Ala | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
ahpC | 2726630 | c.438C>T | synonymous_variant | 0.12 |
thyA | 3073755 | c.717C>T | synonymous_variant | 1.0 |
thyA | 3074283 | c.188delT | frameshift_variant | 0.14 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiA | 3640801 | p.His87Tyr | missense_variant | 0.13 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242680 | p.Ala940Ser | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249111 | c.2598T>C | synonymous_variant | 0.14 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327530 | c.-57G>A | upstream_gene_variant | 0.97 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |