Run ID: SRR21469201
Sample name:
Date: 04-04-2023 02:06:13
Number of reads: 1209858
Percentage reads mapped: 43.18
Strain: La1.7.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.7 | M.bovis | None | None | 1.0 |
La1.7.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.62 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.49 | 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 | 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 | 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 |
ccsA | 619706 | c.-185G>A | upstream_gene_variant | 1.0 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.12 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.19 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.31 |
rpoC | 762917 | c.-453C>A | upstream_gene_variant | 0.36 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.36 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.36 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.36 |
rpoC | 762932 | c.-438G>C | upstream_gene_variant | 0.36 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.4 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.4 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.41 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.39 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.38 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.39 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.38 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.38 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.35 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.34 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.33 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.34 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.37 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.37 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.36 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.38 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.36 |
rpoB | 763077 | p.Val1091Leu | missense_variant | 0.36 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.29 |
rpoB | 763126 | p.Pro1107Gln | missense_variant | 0.26 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.16 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.16 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.16 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.18 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.21 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.21 |
rpoC | 763504 | c.135C>T | synonymous_variant | 0.27 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.26 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 0.27 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 0.29 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.31 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.32 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.34 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.38 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.39 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.39 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.42 |
rpoC | 763614 | c.246_251delGACCCG | disruptive_inframe_deletion | 0.43 |
rpoC | 763622 | p.Ala85Thr | missense_variant | 0.41 |
rpoC | 763627 | c.258_259insAGCTCC | conservative_inframe_insertion | 0.41 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.41 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.4 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.42 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.42 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.42 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.29 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.3 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.28 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.26 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.26 |
rpoC | 763727 | p.Leu120Met | missense_variant | 0.26 |
rpoC | 763732 | c.363C>A | synonymous_variant | 0.23 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.16 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.12 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.2 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>T | synonymous_variant | 0.17 |
rpoC | 764432 | p.Lys355Arg | missense_variant | 0.17 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.17 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.21 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.2 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.21 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.21 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.22 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.31 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.36 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.36 |
rpoC | 764509 | c.1140G>A | synonymous_variant | 0.36 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.34 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.34 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.33 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.33 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.33 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.33 |
rpoC | 764549 | p.Pro394Thr | missense_variant | 0.33 |
rpoC | 764561 | p.Pro398Ala | missense_variant | 0.33 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.33 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.33 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.33 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.34 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.34 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.33 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.33 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.32 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.3 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.31 |
rpoC | 764626 | c.1257C>A | synonymous_variant | 0.28 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.24 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.23 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.17 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.15 |
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 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.21 |
Rv1258c | 1406161 | p.Ala394Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472256 | n.411T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472434 | n.589_590insC | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472437 | n.592T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472438 | n.594delC | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472449 | n.604C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472451 | n.606C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472461 | n.616G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472463 | n.618G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472606 | n.761C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472645 | n.800G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472666 | n.821G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472993 | n.1148G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473134 | n.1289T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473269 | n.1424C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473320 | n.1475G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474291 | n.635_645delTTCCTCTCCGG | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474305 | n.648G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474308 | n.653_654delTG | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474415 | n.758C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474416 | n.761_784delCACGCGCATACGCGCGTGTGAATA | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474770 | n.1113G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475652 | n.1995C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475692 | n.2035G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476104 | n.2448delG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476544 | n.2887T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476566 | n.2909A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476630 | n.2973A>T | non_coding_transcript_exon_variant | 0.26 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.14 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.2 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833862 | c.321G>A | synonymous_variant | 0.2 |
rpsA | 1833883 | c.342C>A | synonymous_variant | 0.15 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.15 |
rpsA | 1833887 | p.Ile116Val | missense_variant | 0.15 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.16 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.16 |
rpsA | 1833907 | p.Lys122Asn | missense_variant | 0.17 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.17 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.17 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.16 |
rpsA | 1833925 | c.384C>T | synonymous_variant | 0.16 |
rpsA | 1833952 | c.411C>A | synonymous_variant | 0.2 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.2 |
rpsA | 1833959 | p.Leu140Val | missense_variant | 0.2 |
rpsA | 1833970 | c.429G>A | synonymous_variant | 0.2 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.19 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.2 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.19 |
rpsA | 1833998 | p.Val153Ile | missense_variant | 0.19 |
rpsA | 1834004 | p.Met155Leu | missense_variant | 0.17 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.18 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.17 |
rpsA | 1834025 | p.Gln162Thr | missense_variant | 0.16 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.16 |
rpsA | 1834034 | p.Ile165Leu | missense_variant | 0.16 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.17 |
rpsA | 1834061 | p.Ile174Leu | missense_variant | 0.17 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.15 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103092 | c.-50T>C | upstream_gene_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
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 |
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 |
fbiB | 3642478 | p.Asp315Ala | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.12 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.14 |
clpC1 | 4039711 | p.Ile332Phe | missense_variant | 0.16 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.17 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.12 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.13 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.13 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.13 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.13 |
clpC1 | 4039772 | p.Lys311Leu | missense_variant | 0.12 |
clpC1 | 4039775 | c.930G>T | synonymous_variant | 0.12 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.12 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.13 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.13 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.13 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.13 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.15 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.14 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.2 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.2 |
clpC1 | 4039853 | p.Leu284Val | missense_variant | 0.2 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.21 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.21 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.21 |
clpC1 | 4039887 | p.Leu273Thr | missense_variant | 0.21 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.21 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.25 |
clpC1 | 4039901 | c.804C>T | synonymous_variant | 0.25 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.26 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.17 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.16 |
clpC1 | 4039937 | p.Val256Ile | missense_variant | 0.16 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.16 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.15 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.15 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.15 |
clpC1 | 4039960 | p.Thr249Ser | missense_variant | 0.14 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.13 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.14 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.14 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.14 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.14 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.14 |
clpC1 | 4040021 | c.684A>G | synonymous_variant | 0.14 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.13 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.18 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.13 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_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 |
aftB | 4267100 | c.1737C>T | synonymous_variant | 1.0 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
fbiC | 1305494 | c.2565_*56delCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |