Run ID: SRR8692887
Sample name:
Date: 13-08-2023 22:47:33
Number of reads: NA
Percentage reads mapped: NA
Strain:
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.07 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.5 | linezolid |
ethA | 4326646 | p.Tyr276* | stop_gained | 0.25 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5293 | c.54C>A | synonymous_variant | 0.15 |
gyrB | 5374 | c.135C>A | synonymous_variant | 0.33 |
gyrB | 5727 | p.Pro163Leu | missense_variant | 0.15 |
gyrB | 5839 | c.600C>A | synonymous_variant | 0.25 |
gyrB | 6133 | c.894G>C | synonymous_variant | 0.17 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.25 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.23 |
gyrB | 6202 | c.963C>G | synonymous_variant | 0.23 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.23 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.26 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.26 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.27 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.25 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.26 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.26 |
gyrB | 6265 | c.1026C>T | synonymous_variant | 0.26 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.26 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.27 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.23 |
gyrB | 6292 | c.1053G>T | synonymous_variant | 0.19 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.16 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.16 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.19 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.19 |
gyrB | 6324 | c.1086dupC | frameshift_variant | 0.17 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.15 |
gyrA | 6475 | c.-827C>G | upstream_gene_variant | 0.12 |
gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.16 |
gyrA | 6550 | c.-752A>T | upstream_gene_variant | 0.14 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.14 |
gyrA | 6565 | c.-737G>C | upstream_gene_variant | 0.22 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.22 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.26 |
gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.26 |
gyrA | 6586 | c.-716T>C | upstream_gene_variant | 0.28 |
gyrB | 6590 | p.Arg451Ser | missense_variant | 0.26 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.16 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.16 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.15 |
gyrA | 6619 | c.-683T>C | upstream_gene_variant | 0.15 |
gyrA | 6631 | c.-671C>T | upstream_gene_variant | 0.2 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.17 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.17 |
gyrA | 6640 | c.-662A>C | upstream_gene_variant | 0.18 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.18 |
gyrA | 6646 | c.-656C>T | upstream_gene_variant | 0.17 |
gyrA | 6649 | c.-653T>G | upstream_gene_variant | 0.2 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.21 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.2 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.18 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.12 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.3 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.13 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.14 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.2 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.27 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.27 |
gyrA | 7424 | c.123G>T | synonymous_variant | 0.27 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.27 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.25 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.25 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.25 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.29 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.33 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.31 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.25 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.33 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.46 |
gyrA | 7506 | p.Ser69Gly | missense_variant | 0.46 |
gyrA | 7520 | c.219G>C | synonymous_variant | 0.45 |
gyrA | 7526 | c.225G>T | synonymous_variant | 0.45 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.5 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.36 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.42 |
gyrA | 7553 | c.252C>T | synonymous_variant | 0.4 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.4 |
gyrA | 7569 | p.Ala90Leu | missense_variant | 0.4 |
gyrA | 7574 | c.273G>A | synonymous_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.53 |
gyrA | 7592 | c.291G>C | synonymous_variant | 0.53 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.56 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.56 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.63 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.58 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.5 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.47 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.5 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.5 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.5 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.5 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.5 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.47 |
gyrA | 7700 | c.399G>T | synonymous_variant | 0.5 |
gyrA | 7706 | c.405C>T | synonymous_variant | 0.47 |
gyrA | 7709 | c.408G>A | synonymous_variant | 0.47 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.47 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.5 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.57 |
gyrA | 7752 | p.Asp151Asn | missense_variant | 0.36 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.31 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.25 |
gyrA | 7775 | c.474C>G | synonymous_variant | 0.25 |
gyrA | 7778 | c.477G>C | synonymous_variant | 0.25 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.25 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.23 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.2 |
gyrA | 7802 | c.501C>G | synonymous_variant | 0.2 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.19 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.18 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.2 |
gyrA | 7841 | c.540C>T | synonymous_variant | 0.2 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.13 |
gyrA | 8152 | p.Ile284Thr | missense_variant | 0.18 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.14 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.18 |
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.17 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.15 |
gyrA | 8402 | p.Asp367Glu | missense_variant | 0.16 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 0.17 |
gyrA | 8417 | c.1116C>G | synonymous_variant | 0.14 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.2 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.15 |
gyrA | 8433 | p.Thr378Arg | missense_variant | 0.16 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.18 |
gyrA | 8450 | c.1149G>A | synonymous_variant | 0.18 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.21 |
gyrA | 8456 | c.1155C>T | synonymous_variant | 0.2 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.19 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.22 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.26 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.26 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.17 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.18 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.18 |
gyrA | 8531 | c.1230G>C | synonymous_variant | 0.18 |
gyrA | 8536 | p.Glu412Ala | missense_variant | 0.14 |
gyrA | 8542 | p.Val414Ala | missense_variant | 0.14 |
gyrA | 8547 | p.Ile416Val | missense_variant | 0.16 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.14 |
gyrA | 8557 | p.Ala419Gly | missense_variant | 0.14 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.13 |
gyrA | 8567 | p.Ile422Met | missense_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.33 |
gyrA | 9389 | c.2088C>A | synonymous_variant | 0.17 |
fgd1 | 491093 | p.Gly104Val | missense_variant | 0.15 |
fgd1 | 491218 | p.Asp146Tyr | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.36 |
mshA | 575205 | c.-143C>A | upstream_gene_variant | 0.14 |
mshA | 575680 | c.333C>T | synonymous_variant | 0.18 |
mshA | 575686 | c.339G>C | synonymous_variant | 0.2 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.22 |
mshA | 575692 | c.345G>C | synonymous_variant | 0.2 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.22 |
mshA | 575704 | c.357T>A | synonymous_variant | 0.2 |
mshA | 575705 | c.358_360delTTGinsCTC | synonymous_variant | 0.2 |
mshA | 575714 | p.Tyr123Asn | missense_variant | 0.17 |
mshA | 576487 | c.1140G>A | synonymous_variant | 0.18 |
mshA | 576492 | p.Arg382His | missense_variant | 0.18 |
ccsA | 620148 | c.258G>T | synonymous_variant | 0.15 |
ccsA | 620271 | c.381C>A | synonymous_variant | 0.25 |
ccsA | 620294 | p.Arg135Gln | missense_variant | 0.29 |
ccsA | 620304 | p.Trp138Cys | missense_variant | 0.29 |
ccsA | 620321 | p.Pro144Gln | missense_variant | 0.4 |
ccsA | 620345 | p.Ser152Tyr | missense_variant | 0.29 |
ccsA | 620461 | p.Val191Phe | missense_variant | 0.25 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.16 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.14 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.17 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.18 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.22 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.2 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.13 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.13 |
rpoB | 760318 | p.Ser171Thr | missense_variant | 0.13 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.13 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.14 |
rpoB | 760354 | p.Glu183Ala | missense_variant | 0.12 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.13 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.15 |
rpoB | 760580 | p.Lys258Asn | missense_variant | 0.18 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.2 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.25 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.21 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.21 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.23 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.2 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.25 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.25 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.27 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.27 |
rpoB | 760715 | c.909C>T | synonymous_variant | 0.43 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.4 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.4 |
rpoB | 760748 | c.942C>G | synonymous_variant | 0.33 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.33 |
rpoB | 760755 | p.His317Asn | missense_variant | 0.27 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.27 |
rpoB | 760764 | p.Glu320Gln | missense_variant | 0.27 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.27 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.27 |
rpoB | 760776 | p.Ser324Asn | missense_variant | 0.27 |
rpoB | 760796 | c.990A>G | synonymous_variant | 0.36 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.3 |
rpoB | 760808 | c.1002C>G | synonymous_variant | 0.38 |
rpoB | 760811 | c.1005C>G | synonymous_variant | 0.33 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.3 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.33 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.27 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.33 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.31 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.23 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.23 |
rpoB | 760877 | c.1071G>T | synonymous_variant | 0.23 |
rpoB | 760880 | c.1074G>C | synonymous_variant | 0.2 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.2 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.2 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.2 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.24 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.24 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.24 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.22 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.2 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.18 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.19 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.2 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.18 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.18 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.21 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.19 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.19 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.19 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.19 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.18 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.17 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.14 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.16 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.16 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.17 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.18 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.18 |
rpoB | 761355 | p.Val517Leu | missense_variant | 0.13 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.13 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.12 |
rpoB | 761367 | p.Glu521Gln | missense_variant | 0.13 |
rpoB | 761374 | p.Val523Asp | missense_variant | 0.14 |
rpoB | 761516 | c.1710G>T | synonymous_variant | 0.2 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.13 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.13 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.14 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.12 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.12 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.33 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.29 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.29 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.43 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.43 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.33 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.26 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.28 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.28 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.3 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.26 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.22 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.22 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.21 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.2 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.19 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.16 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.17 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.12 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.12 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.13 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.12 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.14 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.14 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.2 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.2 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.25 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.24 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.24 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.3 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.3 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.28 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.36 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.3 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.27 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.25 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.24 |
rpoC | 763079 | c.-291C>G | upstream_gene_variant | 0.24 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.24 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.24 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.17 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.25 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.24 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.27 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.36 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.33 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.28 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.21 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.2 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.19 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.19 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.2 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.24 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.14 |
rpoC | 763851 | p.Ala161Asp | missense_variant | 0.15 |
rpoC | 763867 | c.498C>A | synonymous_variant | 0.15 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.17 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.12 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.14 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.14 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.13 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.13 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.14 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.13 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.13 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.22 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.2 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.2 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.16 |
rpoC | 764652 | p.Ser428* | stop_gained | 0.16 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.15 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.17 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.25 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.23 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.18 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.15 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.15 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.39 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.39 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.41 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.42 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.39 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.41 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.38 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.4 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.4 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.4 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.4 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.43 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.38 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.18 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.18 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.2 |
rpoC | 765004 | c.1635G>T | synonymous_variant | 0.18 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.18 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.18 |
rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 0.18 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.17 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.17 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.18 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.17 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.17 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.15 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.16 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.16 |
rpoC | 765070 | c.1701G>T | synonymous_variant | 0.17 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.17 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.17 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.16 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.16 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.16 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.14 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.24 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.33 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.35 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.36 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.36 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.29 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.27 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.27 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.26 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.26 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.26 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.25 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.21 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.21 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.21 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.14 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.14 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.13 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.14 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.14 |
rpoC | 766777 | c.3408C>G | synonymous_variant | 0.14 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.15 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.15 |
rpoC | 766807 | c.3438T>C | synonymous_variant | 0.14 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.15 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.16 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.17 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.25 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.25 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.26 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.3 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.13 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.2 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.18 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.17 |
rpoC | 767186 | p.Gln1273Asn | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.22 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.22 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.56 |
mmpL5 | 775889 | c.2592C>G | synonymous_variant | 0.14 |
mmpL5 | 775905 | p.Lys859Arg | missense_variant | 0.13 |
mmpL5 | 775909 | p.Leu858Ile | missense_variant | 0.17 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.17 |
mmpL5 | 775949 | c.2532G>C | synonymous_variant | 0.14 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.36 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.42 |
mmpL5 | 775970 | c.2511G>C | synonymous_variant | 0.17 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.35 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.16 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.24 |
mmpL5 | 776000 | c.2481G>C | synonymous_variant | 0.19 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.15 |
mmpL5 | 776039 | c.2442C>G | synonymous_variant | 0.18 |
mmpL5 | 776048 | c.2433G>C | synonymous_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.17 |
mmpR5 | 779460 | p.Tyr157* | stop_gained | 0.22 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.42 |
rpsL | 781532 | c.-28G>T | upstream_gene_variant | 0.15 |
rpsL | 781608 | p.Ser17Gly | missense_variant | 0.17 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.13 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.12 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.12 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.14 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.14 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.14 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.14 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.26 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.27 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.28 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.27 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.3 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.3 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.31 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.32 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.31 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.33 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.32 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.28 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.28 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.15 |
rplC | 800678 | c.-131C>T | upstream_gene_variant | 0.17 |
rplC | 800684 | c.-125G>A | upstream_gene_variant | 0.19 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.2 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.2 |
rplC | 800703 | c.-106_-104delTTGinsCTT | upstream_gene_variant | 0.21 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.2 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.2 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.22 |
rplC | 800726 | c.-83G>A | upstream_gene_variant | 0.22 |
rplC | 800744 | c.-65G>C | upstream_gene_variant | 0.24 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.22 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.14 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.14 |
rplC | 800768 | c.-41C>A | upstream_gene_variant | 0.22 |
rplC | 800931 | c.123G>T | synonymous_variant | 0.15 |
rplC | 801003 | c.195G>T | synonymous_variant | 0.2 |
fbiC | 1303326 | c.396C>A | synonymous_variant | 0.22 |
fbiC | 1303387 | p.Ala153Ser | missense_variant | 0.18 |
fbiC | 1303686 | c.756C>A | synonymous_variant | 0.18 |
fbiC | 1304911 | p.Leu661Met | missense_variant | 0.17 |
fbiC | 1305387 | p.Met819Ile | missense_variant | 0.2 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.7 |
Rv1258c | 1406933 | c.408C>A | synonymous_variant | 0.14 |
Rv1258c | 1406989 | p.Pro118Thr | missense_variant | 0.15 |
embR | 1416821 | p.Ala176Asp | missense_variant | 0.15 |
embR | 1416914 | p.Trp145Leu | missense_variant | 0.15 |
embR | 1417250 | p.Pro33His | missense_variant | 0.15 |
rrs | 1471655 | n.-191G>T | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474059 | n.402C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474100 | n.443C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474418 | n.761C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474419 | n.762A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474420 | n.764_766delGCG | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474426 | n.769T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474428 | n.771C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474430 | n.773C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474432 | n.775C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474433 | n.776G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474434 | n.777T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475232 | n.1575A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475296 | n.1639G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476711 | n.3054G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476719 | n.3062C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476741 | n.3084G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476743 | n.3086A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476744 | n.3087G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.13 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.13 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.14 |
inhA | 1674804 | c.603G>C | synonymous_variant | 0.13 |
inhA | 1674810 | c.609C>G | synonymous_variant | 0.14 |
inhA | 1674822 | c.621C>G | synonymous_variant | 0.2 |
inhA | 1674827 | p.Glu209Ala | missense_variant | 0.2 |
inhA | 1674839 | p.Ala213Asp | missense_variant | 0.2 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.2 |
inhA | 1674848 | p.Gln216Arg | missense_variant | 0.2 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.22 |
inhA | 1674879 | c.678T>A | synonymous_variant | 0.22 |
inhA | 1674883 | p.Ile228Val | missense_variant | 0.22 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.17 |
inhA | 1674909 | c.708G>C | synonymous_variant | 0.14 |
inhA | 1674915 | c.714C>G | synonymous_variant | 0.14 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.12 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.12 |
rpsA | 1833616 | c.75A>G | synonymous_variant | 0.15 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.15 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.17 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.17 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.2 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.2 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.17 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.17 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.16 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.2 |
rpsA | 1833727 | c.186G>A | synonymous_variant | 0.21 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.19 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.24 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.25 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.25 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.26 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.26 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.27 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.27 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.3 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.33 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.36 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.39 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.3 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.31 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.27 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.31 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.3 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.21 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.15 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.15 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.13 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.22 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.22 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.24 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.19 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.14 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.2 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.21 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.24 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.22 |
rpsA | 1834135 | c.594G>T | synonymous_variant | 0.22 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.13 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.25 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.21 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.17 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.17 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.18 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.17 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.17 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.2 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.21 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.27 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.31 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.31 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.25 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.25 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.29 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.31 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.3 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.31 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.3 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.29 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.27 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.18 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.19 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.17 |
rpsA | 1834623 | p.Ser361Cys | missense_variant | 0.13 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.14 |
tlyA | 1918359 | c.420A>G | synonymous_variant | 0.2 |
tlyA | 1918625 | p.Pro229Gln | missense_variant | 0.15 |
ndh | 2101738 | p.Gln435His | missense_variant | 0.22 |
ndh | 2102142 | p.Gly301Cys | missense_variant | 0.15 |
ndh | 2102307 | p.Gly246Cys | missense_variant | 0.22 |
ndh | 2102463 | p.Glu194* | stop_gained | 0.18 |
ndh | 2102480 | p.Gln188Pro | missense_variant | 0.17 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 0.17 |
ndh | 2103114 | c.-72G>T | upstream_gene_variant | 0.17 |
katG | 2153910 | c.2202C>A | synonymous_variant | 0.17 |
katG | 2154896 | p.Asp406Asn | missense_variant | 0.17 |
katG | 2154938 | p.Arg392Trp | missense_variant | 0.17 |
katG | 2154941 | p.Glu391* | stop_gained | 0.18 |
katG | 2155037 | p.Ala359Thr | missense_variant | 0.2 |
katG | 2155930 | p.Ala61Glu | missense_variant | 0.18 |
katG | 2156409 | c.-298G>T | upstream_gene_variant | 0.25 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 0.18 |
PPE35 | 2168834 | c.1779G>A | synonymous_variant | 0.25 |
PPE35 | 2169718 | p.Asn299Asp | missense_variant | 0.12 |
PPE35 | 2169759 | p.Gly285Asp | missense_variant | 0.14 |
Rv1979c | 2221822 | p.Ser448* | stop_gained | 0.18 |
Rv1979c | 2221965 | p.Gln400His | missense_variant | 0.25 |
Rv1979c | 2221974 | c.1191G>T | synonymous_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.19 |
pncA | 2288968 | p.Ala92Ser | missense_variant | 0.18 |
pncA | 2289071 | p.His57Gln | missense_variant | 0.13 |
pncA | 2289505 | c.-264G>T | upstream_gene_variant | 0.18 |
pncA | 2290083 | c.-842G>T | upstream_gene_variant | 0.18 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.13 |
kasA | 2518573 | c.459G>C | synonymous_variant | 0.13 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.12 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.13 |
kasA | 2518582 | c.468G>C | synonymous_variant | 0.13 |
kasA | 2518583 | p.Gln157Glu | missense_variant | 0.13 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.13 |
kasA | 2518603 | c.489G>C | synonymous_variant | 0.13 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.13 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.13 |
kasA | 2518612 | c.498C>G | synonymous_variant | 0.13 |
kasA | 2518615 | c.501G>C | synonymous_variant | 0.13 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.14 |
kasA | 2518644 | p.Ala177Gly | missense_variant | 0.12 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.13 |
kasA | 2518701 | p.Gly196Asp | missense_variant | 0.18 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.14 |
kasA | 2519152 | c.1038G>T | synonymous_variant | 0.22 |
kasA | 2519160 | p.Ala349Val | missense_variant | 0.22 |
eis | 2715055 | p.Arg93Gln | missense_variant | 0.15 |
eis | 2715399 | c.-67T>A | upstream_gene_variant | 0.25 |
folC | 2746562 | p.Pro346Arg | missense_variant | 0.12 |
folC | 2747041 | c.558G>T | synonymous_variant | 0.15 |
ribD | 2986822 | c.-17G>T | upstream_gene_variant | 0.14 |
ribD | 2986994 | c.156C>A | synonymous_variant | 0.18 |
ribD | 2987067 | p.Leu77Ile | missense_variant | 0.25 |
ribD | 2987075 | p.Asp79Glu | missense_variant | 0.29 |
ribD | 2987217 | p.Asp127Tyr | missense_variant | 0.18 |
ribD | 2987588 | c.750C>T | synonymous_variant | 0.17 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.17 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.17 |
Rv2752c | 3065076 | c.1116T>G | synonymous_variant | 0.18 |
Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 0.16 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.17 |
Rv2752c | 3065097 | c.1095C>T | synonymous_variant | 0.19 |
Rv2752c | 3065106 | c.1086C>G | synonymous_variant | 0.2 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGG | synonymous_variant | 0.19 |
Rv2752c | 3065120 | p.Ile358Val | missense_variant | 0.21 |
Rv2752c | 3065130 | c.1062A>G | synonymous_variant | 0.21 |
Rv2752c | 3065133 | c.1059T>C | synonymous_variant | 0.22 |
Rv2752c | 3065142 | c.1050A>G | synonymous_variant | 0.21 |
Rv2752c | 3065163 | c.1029C>T | synonymous_variant | 0.17 |
Rv2752c | 3065178 | c.1014G>C | synonymous_variant | 0.13 |
thyA | 3073966 | p.Asp169Ala | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.27 |
ald | 3087056 | c.237G>T | synonymous_variant | 0.17 |
ald | 3087084 | p.Gln89Lys | missense_variant | 0.17 |
fbiD | 3339106 | c.-12C>A | upstream_gene_variant | 0.17 |
fbiD | 3339594 | p.His159Gln | missense_variant | 0.14 |
Rv3083 | 3448704 | c.201C>A | synonymous_variant | 0.17 |
Rv3083 | 3448706 | p.Pro68Gln | missense_variant | 0.17 |
Rv3083 | 3449542 | p.Gly347Cys | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.29 |
fprA | 3474132 | p.Leu42Phe | missense_variant | 0.14 |
Rv3236c | 3612546 | p.Ala191Thr | missense_variant | 0.15 |
Rv3236c | 3612603 | p.Leu172Ile | missense_variant | 0.17 |
fbiA | 3640642 | p.His34Asn | missense_variant | 0.14 |
fbiB | 3641736 | p.Glu68* | stop_gained | 0.23 |
rpoA | 3877526 | p.Gly328Cys | missense_variant | 0.17 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.12 |
rpoA | 3877584 | c.924C>G | synonymous_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.17 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.21 |
rpoA | 3877602 | c.906C>T | synonymous_variant | 0.2 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.18 |
rpoA | 3877620 | p.Glu296Asp | missense_variant | 0.14 |
rpoA | 3877638 | c.870T>G | synonymous_variant | 0.21 |
rpoA | 3877647 | c.861C>T | synonymous_variant | 0.17 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.14 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.14 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.14 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.18 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.28 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.29 |
rpoA | 3877842 | c.666A>T | synonymous_variant | 0.29 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.32 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.3 |
rpoA | 3877860 | c.648C>T | synonymous_variant | 0.33 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.29 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.26 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.24 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.23 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.23 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.17 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.22 |
rpoA | 3878248 | p.Ser87* | stop_gained | 0.29 |
ddn | 3986921 | c.78C>A | synonymous_variant | 0.14 |
ddn | 3986934 | p.Arg31Ser | missense_variant | 0.17 |
ddn | 3987124 | p.Ala94Asp | missense_variant | 0.15 |
ddn | 3987292 | p.Glu150Gly | missense_variant | 0.12 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.17 |
clpC1 | 4038587 | c.2118C>T | synonymous_variant | 0.22 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.25 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.29 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.29 |
clpC1 | 4038614 | c.2091C>T | synonymous_variant | 0.29 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 0.27 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.27 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.27 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.29 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.27 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.27 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.25 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.24 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.24 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.22 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.24 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.2 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.25 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.23 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.23 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.23 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.23 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.25 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.25 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.23 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.23 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.21 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.19 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.17 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.18 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.14 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.14 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.16 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.16 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.15 |
clpC1 | 4039001 | p.Asn568Ala | missense_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.22 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.29 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.33 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.35 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.35 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.35 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.29 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.31 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.33 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.44 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.44 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.35 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.35 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.38 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.35 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.3 |
clpC1 | 4039262 | c.1443C>T | synonymous_variant | 0.3 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.24 |
clpC1 | 4039277 | c.1428C>A | synonymous_variant | 0.24 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.22 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.22 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.22 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.21 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.21 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.25 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.26 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.25 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.23 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.19 |
clpC1 | 4039347 | p.Arg453Lys | missense_variant | 0.2 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.19 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.2 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.17 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.17 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.12 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.12 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.12 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.12 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.13 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.14 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.19 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.18 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.17 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.17 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.17 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.21 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.22 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.25 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.18 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.18 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.19 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.18 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.18 |
clpC1 | 4039571 | c.1134G>C | synonymous_variant | 0.19 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.2 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.2 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.24 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 0.24 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.18 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.19 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.2 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.13 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.14 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.14 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.17 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.2 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.33 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.33 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.36 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.36 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.31 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.31 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.29 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.33 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.28 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.22 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.26 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.25 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.32 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.29 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.28 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.24 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.15 |
clpC1 | 4040090 | p.Ser205Cys | missense_variant | 0.16 |
clpC1 | 4040093 | c.612C>T | synonymous_variant | 0.2 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.25 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.27 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.3 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.32 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.3 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.29 |
clpC1 | 4040195 | c.510G>C | synonymous_variant | 0.22 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.21 |
clpC1 | 4040201 | c.504C>A | synonymous_variant | 0.21 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.2 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.2 |
clpC1 | 4040213 | p.Ser164Asn | missense_variant | 0.21 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.23 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.22 |
clpC1 | 4040246 | c.459C>A | synonymous_variant | 0.17 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.17 |
clpC1 | 4040258 | c.447G>A | synonymous_variant | 0.17 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.17 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.17 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.17 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.17 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.21 |
clpC1 | 4040558 | c.147G>C | synonymous_variant | 0.21 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.25 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.2 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.17 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.22 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.24 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.21 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.21 |
clpC1 | 4040600 | c.103_105delTTAinsCTC | synonymous_variant | 0.22 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.21 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.2 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.15 |
clpC1 | 4040648 | c.57G>A | synonymous_variant | 0.15 |
clpC1 | 4040862 | c.-158C>A | upstream_gene_variant | 0.15 |
embC | 4239885 | p.Pro8His | missense_variant | 0.18 |
embC | 4240103 | p.Asp81Tyr | missense_variant | 0.17 |
embC | 4240139 | p.Gly93* | stop_gained | 0.2 |
embC | 4241944 | c.2082C>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.44 |
embA | 4242652 | c.-581C>G | upstream_gene_variant | 0.13 |
embA | 4242898 | c.-335G>T | upstream_gene_variant | 0.14 |
embA | 4243813 | p.Arg194Leu | missense_variant | 0.18 |
embA | 4245089 | c.1857G>T | synonymous_variant | 0.17 |
embA | 4246437 | p.Ala1069Ser | missense_variant | 0.14 |
embB | 4246649 | p.Leu46Met | missense_variant | 0.14 |
embB | 4246698 | p.Gly62Val | missense_variant | 0.15 |
embB | 4247458 | p.Tyr315* | stop_gained | 0.5 |
embB | 4249045 | p.Leu844Phe | missense_variant | 0.17 |
embB | 4249570 | c.3057G>T | synonymous_variant | 0.17 |
embB | 4249759 | c.3246C>A | synonymous_variant | 0.17 |
embB | 4249766 | p.Arg1085Ser | missense_variant | 0.17 |
embB | 4249806 | p.Pro1098Gln | missense_variant | 0.25 |
aftB | 4267331 | c.1506C>A | synonymous_variant | 0.21 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.15 |
aftB | 4268219 | c.618C>A | synonymous_variant | 0.4 |
aftB | 4268229 | p.Ala203Asp | missense_variant | 0.4 |
aftB | 4268345 | c.492C>A | synonymous_variant | 0.22 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 0.17 |
aftB | 4269072 | c.-236G>C | upstream_gene_variant | 0.12 |
aftB | 4269084 | c.-248G>C | upstream_gene_variant | 0.14 |
aftB | 4269087 | c.-251G>C | upstream_gene_variant | 0.14 |
aftB | 4269099 | c.-263G>T | upstream_gene_variant | 0.14 |
ubiA | 4269102 | p.Ser244Gly | missense_variant | 0.14 |
ubiA | 4269106 | p.Tyr243Ser | missense_variant | 0.14 |
aftB | 4269117 | c.-281G>A | upstream_gene_variant | 0.2 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.2 |
aftB | 4269129 | c.-293G>C | upstream_gene_variant | 0.2 |
aftB | 4269141 | c.-307_-305delTTGinsCTC | upstream_gene_variant | 0.24 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.21 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.24 |
aftB | 4269171 | c.-335C>G | upstream_gene_variant | 0.28 |
aftB | 4269177 | c.-341G>C | upstream_gene_variant | 0.26 |
ubiA | 4269186 | p.Thr216Ser | missense_variant | 0.31 |
ubiA | 4269199 | p.Ser212Asn | missense_variant | 0.19 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.19 |
aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.2 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.19 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.19 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.2 |
ubiA | 4269238 | p.Ala199Val | missense_variant | 0.2 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.2 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.2 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.21 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.2 |
aftB | 4269264 | c.-428C>T | upstream_gene_variant | 0.19 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 0.13 |
ethA | 4326541 | p.Glu311Asp | missense_variant | 0.14 |
ethA | 4326563 | p.Ala304Asp | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.31 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.12 |
gid | 4407624 | c.579G>T | synonymous_variant | 0.15 |