Run ID: SRR8692905
Sample name:
Date: 13-08-2023 20:12:59
Number of reads: NA
Percentage reads mapped: NA
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.78 | linezolid |
katG | 2155501 | p.Trp204* | stop_gained | 0.22 | isoniazid |
ddn | 3987085 | p.Gly81Asp | missense_variant | 0.14 | delamanid |
ethA | 4326426 | c.1047delT | frameshift_variant | 0.2 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5064 | c.-176C>A | upstream_gene_variant | 0.2 |
gyrB | 5867 | p.Asp210Tyr | missense_variant | 0.25 |
gyrB | 6002 | p.Gly255Cys | missense_variant | 0.17 |
gyrB | 6067 | c.828G>T | synonymous_variant | 0.2 |
gyrB | 6082 | p.Lys281Asn | missense_variant | 0.22 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.22 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.22 |
gyrB | 6200 | c.961_963delCGCinsAGG | synonymous_variant | 0.22 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.22 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.2 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.2 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.23 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.23 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.23 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.23 |
gyrB | 6265 | c.1026C>T | synonymous_variant | 0.17 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.18 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6292 | c.1053G>T | synonymous_variant | 0.18 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.18 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.2 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.27 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.18 |
gyrB | 6324 | c.1086dupC | frameshift_variant | 0.18 |
gyrB | 6328 | c.1090delG | frameshift_variant | 0.18 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.18 |
gyrA | 6550 | c.-752A>T | upstream_gene_variant | 0.17 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.17 |
gyrA | 6565 | c.-737G>C | upstream_gene_variant | 0.17 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.17 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.23 |
gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.2 |
gyrA | 6586 | c.-716T>C | upstream_gene_variant | 0.2 |
gyrB | 6590 | p.Arg451Ser | missense_variant | 0.2 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.12 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.12 |
gyrA | 6619 | c.-683T>C | upstream_gene_variant | 0.12 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.12 |
gyrA | 6649 | c.-653T>G | upstream_gene_variant | 0.12 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.12 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.17 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.17 |
gyrB | 6723 | p.Arg495Leu | missense_variant | 0.5 |
gyrA | 6832 | c.-470C>A | upstream_gene_variant | 0.4 |
gyrA | 6943 | c.-359G>T | upstream_gene_variant | 0.33 |
gyrA | 7165 | c.-137C>A | upstream_gene_variant | 0.17 |
gyrB | 7167 | p.Ala643Asp | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.69 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.2 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.2 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.22 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.25 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.25 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.25 |
gyrA | 7424 | c.123G>T | synonymous_variant | 0.23 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.3 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.25 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.27 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.25 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.23 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.21 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.23 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.25 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.23 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.23 |
gyrA | 7506 | p.Ser69Gly | missense_variant | 0.23 |
gyrA | 7520 | c.219G>C | synonymous_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.25 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.14 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.14 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.14 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.15 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.15 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.15 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.17 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.23 |
gyrA | 7700 | c.399G>T | synonymous_variant | 0.23 |
gyrA | 7706 | c.405C>T | synonymous_variant | 0.21 |
gyrA | 7709 | c.408G>A | synonymous_variant | 0.23 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.23 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.23 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.21 |
gyrA | 7752 | p.Asp151Asn | missense_variant | 0.33 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.38 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.43 |
gyrA | 7775 | c.474C>G | synonymous_variant | 0.33 |
gyrA | 7778 | c.477G>C | synonymous_variant | 0.33 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.33 |
gyrA | 8021 | c.720C>A | synonymous_variant | 0.33 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.12 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.12 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.15 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.14 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.15 |
gyrA | 8531 | c.1230G>C | synonymous_variant | 0.15 |
gyrA | 8536 | p.Glu412Ala | missense_variant | 0.12 |
gyrA | 8542 | p.Val414Ala | missense_variant | 0.12 |
gyrA | 8547 | p.Ile416Val | missense_variant | 0.12 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.13 |
gyrA | 8557 | p.Ala419Gly | missense_variant | 0.12 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.12 |
gyrA | 8567 | p.Ile422Met | missense_variant | 0.12 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.15 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.14 |
gyrA | 8649 | p.Arg450Ser | missense_variant | 0.15 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.12 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.14 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.14 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.13 |
gyrA | 9072 | p.Ala591Ser | missense_variant | 0.17 |
gyrA | 9086 | c.1785C>T | synonymous_variant | 0.18 |
gyrA | 9128 | c.1827C>A | synonymous_variant | 0.22 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.27 |
gyrA | 9596 | c.2295G>C | synonymous_variant | 0.2 |
fgd1 | 490602 | c.-181C>T | upstream_gene_variant | 0.2 |
fgd1 | 490906 | p.Gln42Lys | missense_variant | 0.18 |
fgd1 | 490941 | p.Phe53Leu | missense_variant | 0.18 |
fgd1 | 491002 | p.Val74Leu | missense_variant | 0.13 |
fgd1 | 491491 | p.Pro237Thr | missense_variant | 0.15 |
fgd1 | 491496 | c.714C>T | synonymous_variant | 0.15 |
fgd1 | 491503 | p.Leu241Ala | missense_variant | 0.17 |
fgd1 | 491508 | c.726A>G | synonymous_variant | 0.17 |
fgd1 | 491509 | c.727T>C | synonymous_variant | 0.17 |
fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.17 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.15 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.13 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.13 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.14 |
fgd1 | 491563 | p.Ser261Cys | missense_variant | 0.13 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.12 |
fgd1 | 491610 | c.828A>C | synonymous_variant | 0.13 |
mshA | 575316 | c.-32C>A | upstream_gene_variant | 0.13 |
mshA | 575478 | p.Pro44Leu | missense_variant | 0.2 |
mshA | 575596 | c.249C>A | synonymous_variant | 0.25 |
ccsA | 619763 | c.-128C>A | upstream_gene_variant | 0.18 |
ccsA | 620374 | p.Pro162Thr | missense_variant | 0.29 |
ccsA | 620583 | c.693G>T | synonymous_variant | 0.25 |
ccsA | 620588 | p.Thr233Met | missense_variant | 0.22 |
rpoB | 760198 | p.Ala131Asp | missense_variant | 0.12 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.22 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.25 |
rpoB | 760380 | p.Thr192Asp | missense_variant | 0.25 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.22 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.22 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.33 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.25 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.25 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.38 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.3 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.3 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.3 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.25 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.18 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.18 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.18 |
rpoB | 760535 | c.729C>G | synonymous_variant | 0.18 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.25 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.25 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.2 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.17 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.18 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 760796 | c.990A>G | synonymous_variant | 0.19 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.18 |
rpoB | 760808 | c.1002C>G | synonymous_variant | 0.18 |
rpoB | 760811 | c.1005C>G | synonymous_variant | 0.18 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.18 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.18 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.19 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.22 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.28 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.28 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.28 |
rpoB | 760877 | c.1071G>T | synonymous_variant | 0.31 |
rpoB | 760880 | c.1074G>C | synonymous_variant | 0.31 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.31 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.31 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.31 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.33 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.33 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.31 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.31 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.17 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.17 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.17 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.17 |
rpoB | 760977 | p.Glu391* | stop_gained | 0.17 |
rpoB | 760981 | p.Arg392Leu | missense_variant | 0.2 |
rpoB | 760989 | c.1183C>A | synonymous_variant | 0.22 |
rpoB | 760992 | p.Glu396* | stop_gained | 0.25 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.5 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.5 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.44 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.4 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.4 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.4 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.4 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.4 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.4 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.33 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.33 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.33 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.29 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.4 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.4 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.33 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.29 |
rpoB | 761346 | p.Val514Ile | missense_variant | 0.29 |
rpoB | 761355 | p.Val517Gln | missense_variant | 0.29 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.29 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.29 |
rpoB | 761367 | p.Glu521Gln | missense_variant | 0.29 |
rpoB | 761374 | p.Val523Asp | missense_variant | 0.33 |
rpoB | 761384 | c.1578C>A | synonymous_variant | 0.33 |
rpoB | 761403 | p.His533Asn | missense_variant | 0.29 |
rpoB | 761482 | p.Ala559Val | missense_variant | 0.18 |
rpoB | 761529 | p.Val575Phe | missense_variant | 0.18 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.12 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.17 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.15 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.15 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.16 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.12 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.12 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.12 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.17 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.17 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.19 |
rpoB | 762233 | c.2427G>T | synonymous_variant | 0.15 |
rpoB | 762955 | p.Pro1050Gln | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.27 |
rpoC | 763052 | c.-318G>T | upstream_gene_variant | 0.2 |
rpoB | 763244 | p.Asp1146Glu | missense_variant | 0.22 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.15 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.15 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.17 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.15 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.15 |
rpoC | 763443 | p.Tyr25Phe | missense_variant | 0.2 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.21 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.21 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.19 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.19 |
rpoC | 764017 | c.648G>T | synonymous_variant | 0.25 |
rpoC | 764096 | p.Glu243* | stop_gained | 0.21 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.21 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.2 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.29 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.15 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.23 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.23 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.25 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.25 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.23 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.27 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.27 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.25 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.24 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.25 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.2 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.14 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.13 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.13 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.13 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.17 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.15 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.16 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.14 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.15 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.19 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.19 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.2 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.15 |
rpoC | 764960 | p.Ala531Ser | missense_variant | 0.29 |
rpoC | 765800 | p.Phe811Leu | missense_variant | 0.33 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.38 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.38 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.38 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.38 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.44 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.56 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.67 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.75 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.75 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.86 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.86 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.5 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.33 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.33 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.27 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.25 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.27 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.27 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.27 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.17 |
rpoC | 766659 | p.Arg1097Leu | missense_variant | 0.17 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.14 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.17 |
rpoC | 766711 | c.3342C>T | synonymous_variant | 0.15 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.15 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.15 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.13 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.15 |
rpoC | 766771 | c.3402G>C | synonymous_variant | 0.15 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.14 |
rpoC | 766775 | c.3406_3408delCGCinsAGG | synonymous_variant | 0.14 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.29 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.25 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.25 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.25 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.5 |
mmpL5 | 775687 | p.Leu932Ile | missense_variant | 0.2 |
mmpL5 | 775718 | c.2763C>A | synonymous_variant | 0.2 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.2 |
mmpL5 | 775865 | c.2616T>C | synonymous_variant | 0.2 |
mmpL5 | 775885 | p.Ile866Leu | missense_variant | 0.25 |
mmpL5 | 775886 | c.2595A>T | synonymous_variant | 0.18 |
mmpL5 | 775889 | c.2592C>G | synonymous_variant | 0.14 |
mmpL5 | 775892 | c.2589C>T | synonymous_variant | 0.14 |
mmpL5 | 775907 | p.Leu858Met | missense_variant | 0.18 |
mmpL5 | 775915 | p.Ala856Ser | missense_variant | 0.29 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.33 |
mmpL5 | 775921 | p.Leu854Val | missense_variant | 0.14 |
mmpL5 | 775949 | c.2532G>C | synonymous_variant | 0.19 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.29 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.33 |
mmpL5 | 775972 | p.Ala837Pro | missense_variant | 0.18 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.19 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.33 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.24 |
mmpL5 | 775994 | p.Ile829Met | missense_variant | 0.12 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.35 |
mmpL5 | 776000 | p.Leu827Ile | missense_variant | 0.27 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.25 |
mmpL5 | 776036 | c.2445G>C | synonymous_variant | 0.15 |
mmpL5 | 776564 | c.1917C>A | synonymous_variant | 0.15 |
mmpL5 | 776576 | c.1905C>A | synonymous_variant | 0.18 |
mmpL5 | 776805 | p.Gly559Val | missense_variant | 0.22 |
mmpL5 | 777256 | p.Pro409Ala | missense_variant | 0.13 |
mmpL5 | 778321 | p.Glu54* | stop_gained | 0.2 |
mmpL5 | 778504 | c.-24G>T | upstream_gene_variant | 0.29 |
mmpR5 | 779059 | p.Gly24Cys | missense_variant | 0.14 |
mmpR5 | 779098 | p.Gly37Cys | missense_variant | 0.22 |
mmpR5 | 779109 | p.Leu40Phe | missense_variant | 0.25 |
mmpR5 | 779437 | p.Val150Phe | missense_variant | 0.17 |
mmpS5 | 779567 | c.-664_-662delGCGinsTCT | upstream_gene_variant | 0.17 |
rpsL | 781381 | c.-179C>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.43 |
rpsL | 781623 | p.Ala22Thr | missense_variant | 0.17 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.14 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.13 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.14 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.12 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.13 |
rpsL | 781735 | p.Ser59Thr | missense_variant | 0.13 |
rpsL | 781737 | p.Gln60Gly | missense_variant | 0.14 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
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 | 0.15 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.17 |
rpsL | 781787 | p.Glu76Asp | missense_variant | 0.13 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.13 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.13 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.15 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.14 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.15 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.36 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.33 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.5 |
rplC | 800639 | c.-170C>T | upstream_gene_variant | 0.5 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.62 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.62 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.62 |
rplC | 800678 | c.-131C>T | upstream_gene_variant | 0.27 |
rplC | 800723 | c.-86C>A | upstream_gene_variant | 0.18 |
rplC | 800777 | c.-32C>T | upstream_gene_variant | 0.17 |
rplC | 800935 | p.Glu43* | stop_gained | 0.18 |
rplC | 801252 | c.444G>A | synonymous_variant | 0.25 |
fbiC | 1303064 | p.Ala45Asp | missense_variant | 0.17 |
fbiC | 1303178 | p.Ala83Glu | missense_variant | 0.17 |
fbiC | 1303350 | p.Cys140* | stop_gained | 0.29 |
fbiC | 1303518 | p.Met196Ile | missense_variant | 0.17 |
fbiC | 1303651 | p.Arg241Trp | missense_variant | 0.25 |
fbiC | 1303690 | p.Pro254Thr | missense_variant | 0.17 |
fbiC | 1303710 | p.Leu260Phe | missense_variant | 0.25 |
fbiC | 1305369 | p.Glu813Asp | missense_variant | 0.18 |
Rv1258c | 1406441 | p.Leu300Phe | missense_variant | 0.25 |
Rv1258c | 1406561 | c.780G>T | synonymous_variant | 0.14 |
Rv1258c | 1406659 | p.Leu228Ile | missense_variant | 0.12 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.54 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.2 |
Rv1258c | 1407013 | p.Ala110Ser | missense_variant | 0.4 |
Rv1258c | 1407420 | c.-80C>A | upstream_gene_variant | 0.2 |
embR | 1417176 | p.Ala58Ser | missense_variant | 0.17 |
embR | 1417430 | c.-83C>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472463 | n.618G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472471 | n.626G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472826 | n.981G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473000 | n.1155G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473736 | n.79C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473779 | n.122G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474116 | n.459G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474299 | n.642C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475374 | n.1717G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.5 |
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 | 0.59 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475819 | n.2162C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476370 | n.2713C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476711 | n.3054G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476719 | n.3062C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476741 | n.3084G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476743 | n.3086A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476758 | n.3101G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673192 | c.-248C>A | upstream_gene_variant | 0.13 |
fabG1 | 1673282 | c.-158C>A | upstream_gene_variant | 0.17 |
fabG1 | 1673533 | p.Ala32Ser | missense_variant | 0.36 |
fabG1 | 1673659 | p.Ala74Ser | missense_variant | 0.15 |
rpsA | 1833413 | c.-129G>T | upstream_gene_variant | 0.18 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.15 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.2 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.19 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.19 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.2 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.2 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.2 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.2 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.21 |
rpsA | 1834199 | p.Val220Leu | missense_variant | 0.14 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.12 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.12 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.27 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.31 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.31 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.33 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.33 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.36 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.33 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.33 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.3 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.3 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.36 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.27 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.2 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.25 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.25 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.25 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.25 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.25 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.17 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.17 |
rpsA | 1834565 | p.Asp342Tyr | missense_variant | 0.17 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.14 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.12 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.12 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.14 |
rpsA | 1834705 | c.1164C>G | synonymous_variant | 0.14 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.19 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.2 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.23 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.23 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.21 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.2 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.12 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.13 |
rpsA | 1834835 | p.Met432Leu | missense_variant | 0.15 |
rpsA | 1834922 | p.Gly461Cys | missense_variant | 0.15 |
rpsA | 1834930 | c.1389A>G | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.38 |
tlyA | 1918027 | p.Gly30Cys | missense_variant | 0.13 |
ndh | 2102062 | p.Glu327Asp | missense_variant | 0.23 |
ndh | 2102083 | c.960G>T | synonymous_variant | 0.14 |
ndh | 2102244 | c.799C>A | synonymous_variant | 0.13 |
ndh | 2102392 | c.651C>A | synonymous_variant | 0.17 |
ndh | 2102686 | c.357G>T | synonymous_variant | 0.15 |
katG | 2154402 | c.1710C>A | synonymous_variant | 0.13 |
katG | 2156049 | c.63C>A | synonymous_variant | 0.15 |
katG | 2156216 | c.-105C>A | upstream_gene_variant | 0.15 |
katG | 2156363 | c.-252C>A | upstream_gene_variant | 0.15 |
katG | 2156527 | c.-416C>A | upstream_gene_variant | 0.14 |
katG | 2156552 | c.-441C>A | upstream_gene_variant | 0.18 |
katG | 2156560 | c.-449C>A | upstream_gene_variant | 0.18 |
PPE35 | 2167666 | p.Gln983Lys | missense_variant | 0.13 |
PPE35 | 2168677 | p.Leu646Ile | missense_variant | 0.29 |
PPE35 | 2169587 | c.1026G>C | synonymous_variant | 0.14 |
PPE35 | 2169604 | p.Gly337Cys | missense_variant | 0.13 |
PPE35 | 2170033 | p.Gly194Ser | missense_variant | 0.33 |
PPE35 | 2170619 | c.-7G>T | upstream_gene_variant | 0.15 |
Rv1979c | 2221748 | c.1417C>A | synonymous_variant | 0.15 |
Rv1979c | 2222249 | p.Val306Phe | missense_variant | 0.13 |
Rv1979c | 2222515 | p.Thr217Lys | missense_variant | 0.18 |
Rv1979c | 2222672 | p.Thr165Ala | missense_variant | 0.18 |
Rv1979c | 2222683 | p.Trp161Leu | missense_variant | 0.17 |
Rv1979c | 2222805 | c.360G>T | synonymous_variant | 0.18 |
Rv1979c | 2222837 | p.Ala110Ser | missense_variant | 0.15 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.17 |
kasA | 2518198 | p.Asp28Glu | missense_variant | 0.29 |
kasA | 2518559 | p.Gly149Cys | missense_variant | 0.17 |
kasA | 2519095 | c.981C>G | synonymous_variant | 0.22 |
kasA | 2519105 | p.Cys331Val | missense_variant | 0.2 |
kasA | 2519110 | p.Asp332Glu | missense_variant | 0.17 |
kasA | 2519113 | p.Gln333His | missense_variant | 0.17 |
kasA | 2519137 | c.1023T>G | synonymous_variant | 0.17 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.17 |
kasA | 2519164 | c.1050C>G | synonymous_variant | 0.15 |
kasA | 2519170 | c.1056G>C | synonymous_variant | 0.15 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.15 |
kasA | 2519180 | p.Val356Ile | missense_variant | 0.17 |
kasA | 2519185 | c.1071C>G | synonymous_variant | 0.17 |
kasA | 2519195 | p.Thr361Ala | missense_variant | 0.15 |
kasA | 2519198 | c.1084C>T | synonymous_variant | 0.15 |
kasA | 2519203 | c.1089C>T | synonymous_variant | 0.17 |
kasA | 2519364 | c.1250G>T | stop_lost&splice_region_variant | 0.33 |
eis | 2714645 | p.Arg230Ser | missense_variant | 0.22 |
eis | 2714846 | p.Val163Ile | missense_variant | 0.13 |
ahpC | 2726687 | c.495C>A | synonymous_variant | 0.18 |
folC | 2746998 | p.His201Asn | missense_variant | 0.29 |
pepQ | 2859875 | p.Asp182Tyr | missense_variant | 0.2 |
pepQ | 2860368 | c.51C>T | synonymous_variant | 0.29 |
ribD | 2986950 | p.Gly38Cys | missense_variant | 0.22 |
ribD | 2986963 | p.Arg42Leu | missense_variant | 0.22 |
ribD | 2987246 | c.408C>A | synonymous_variant | 0.18 |
ribD | 2987388 | p.Ala184Ser | missense_variant | 0.15 |
ribD | 2987524 | p.Thr229Lys | missense_variant | 0.14 |
Rv2752c | 3064581 | c.1611C>A | synonymous_variant | 0.25 |
Rv2752c | 3065745 | c.447C>A | synonymous_variant | 0.18 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 0.33 |
ald | 3086645 | c.-175C>A | upstream_gene_variant | 0.25 |
ald | 3086679 | c.-141C>A | upstream_gene_variant | 0.22 |
ald | 3087165 | p.Ala116Ser | missense_variant | 0.4 |
ald | 3087497 | p.Glu226Asp | missense_variant | 0.2 |
fbiD | 3339062 | c.-56G>A | upstream_gene_variant | 0.25 |
fbiD | 3339139 | p.Gly8Cys | missense_variant | 0.17 |
Rv3083 | 3448709 | p.Trp69Leu | missense_variant | 0.25 |
Rv3083 | 3448768 | p.Ala89Ser | missense_variant | 0.2 |
Rv3083 | 3448783 | p.Val94Phe | missense_variant | 0.18 |
Rv3083 | 3448838 | p.Arg112Leu | missense_variant | 0.2 |
Rv3083 | 3448963 | p.Pro154Thr | missense_variant | 0.22 |
Rv3083 | 3449216 | p.Trp238Leu | missense_variant | 0.19 |
Rv3083 | 3449301 | c.798G>T | synonymous_variant | 0.14 |
Rv3083 | 3449961 | c.1458C>T | synonymous_variant | 0.15 |
fprA | 3474379 | p.Ala125Thr | missense_variant | 0.33 |
whiB7 | 3568803 | c.-124G>T | upstream_gene_variant | 0.17 |
whiB7 | 3568810 | c.-131G>T | upstream_gene_variant | 0.15 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.2 |
fbiA | 3640721 | p.Pro60Gln | missense_variant | 0.18 |
fbiA | 3640853 | p.Leu104Pro | missense_variant | 0.25 |
fbiA | 3640999 | p.His153Asn | missense_variant | 0.14 |
fbiA | 3641425 | p.His295Tyr | missense_variant | 0.33 |
fbiB | 3641765 | c.231G>T | synonymous_variant | 0.2 |
fbiB | 3641769 | p.Glu79* | stop_gained | 0.2 |
fbiB | 3641834 | c.300G>T | synonymous_variant | 0.17 |
fbiB | 3641969 | c.435C>A | synonymous_variant | 0.14 |
fbiB | 3641996 | c.462C>T | synonymous_variant | 0.13 |
fbiB | 3642292 | p.Arg253Leu | missense_variant | 0.15 |
fbiB | 3642600 | p.Gly356* | stop_gained | 0.2 |
fbiB | 3642667 | p.Gly378Val | missense_variant | 0.29 |
alr | 3840913 | p.Ala170Ser | missense_variant | 0.18 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.12 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.14 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.15 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.15 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.14 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.17 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.17 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 0.14 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.12 |
rpoA | 3877808 | p.Ile234Val | missense_variant | 0.12 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.14 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.18 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.18 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.25 |
rpoA | 3877860 | c.648C>T | synonymous_variant | 0.27 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.3 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.22 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.25 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.25 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.25 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.22 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.25 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.2 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.2 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.17 |
rpoA | 3877983 | c.525C>G | synonymous_variant | 0.18 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.12 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.13 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.12 |
rpoA | 3878145 | p.Pro121Gln | missense_variant | 0.14 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.18 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.24 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.19 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.12 |
rpoA | 3878197 | p.Glu104Ala | missense_variant | 0.12 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.12 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.12 |
rpoA | 3878502 | c.6G>T | synonymous_variant | 0.18 |
rpoA | 3878605 | c.-98G>T | upstream_gene_variant | 0.29 |
ddn | 3986934 | p.Arg31Cys | missense_variant | 0.22 |
ddn | 3987013 | p.Gly57Asp | missense_variant | 0.2 |
ddn | 3987099 | p.Pro86Thr | missense_variant | 0.15 |
clpC1 | 4038181 | p.Gly842Cys | missense_variant | 0.13 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.14 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.14 |
clpC1 | 4038614 | c.2091C>T | synonymous_variant | 0.15 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 0.15 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.15 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.14 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.15 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.15 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.15 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.15 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.14 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.15 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.15 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.15 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.15 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.14 |
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 | 0.25 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.25 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.23 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.31 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.31 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.28 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.29 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.24 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.25 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.3 |
clpC1 | 4038881 | c.1824C>G | synonymous_variant | 0.3 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.33 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.33 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.36 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.36 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.36 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.36 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.36 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.27 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.3 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.33 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.22 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.22 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.33 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.33 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.38 |
clpC1 | 4039001 | p.Asn568Ala | missense_variant | 0.33 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.29 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.14 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.15 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.17 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.13 |
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 | 0.12 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.17 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.14 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.14 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.13 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.13 |
clpC1 | 4039571 | c.1134G>C | synonymous_variant | 0.13 |
clpC1 | 4039575 | p.Ala377Gly | missense_variant | 0.13 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.13 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.14 |
clpC1 | 4039593 | p.Arg371Leu | missense_variant | 0.13 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 0.14 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.12 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.12 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.14 |
clpC1 | 4039640 | c.1065C>G | synonymous_variant | 0.19 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.14 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.18 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039718 | c.987C>G | synonymous_variant | 0.29 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.31 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.38 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.38 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.4 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.38 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.38 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.38 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.35 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.35 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.38 |
clpC1 | 4039808 | p.Glu299Asp | missense_variant | 0.15 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.46 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.46 |
clpC1 | 4039823 | c.882T>A | synonymous_variant | 0.46 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.46 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.46 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.43 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.36 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.18 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.31 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.31 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.31 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.36 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.36 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.31 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.33 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.27 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.28 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.28 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.31 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.28 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.28 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.29 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.25 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>T | synonymous_variant | 0.17 |
clpC1 | 4040195 | c.510G>C | synonymous_variant | 0.22 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.22 |
clpC1 | 4040201 | c.504C>A | synonymous_variant | 0.22 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.22 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.25 |
clpC1 | 4040213 | p.Ser164Asn | missense_variant | 0.25 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.22 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.22 |
clpC1 | 4040246 | c.459C>A | synonymous_variant | 0.25 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.25 |
clpC1 | 4040258 | c.447G>A | synonymous_variant | 0.25 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.25 |
clpC1 | 4040341 | p.Gln122Lys | missense_variant | 0.33 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.17 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.15 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.14 |
clpC1 | 4040433 | c.271_272delAGinsTC | synonymous_variant | 0.13 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 0.13 |
clpC1 | 4040438 | c.267G>A | synonymous_variant | 0.14 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.17 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.15 |
clpC1 | 4040462 | c.243C>T | synonymous_variant | 0.14 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.14 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.14 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.14 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.19 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.19 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.2 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.2 |
clpC1 | 4040590 | p.His39Asn | missense_variant | 0.2 |
clpC1 | 4040636 | c.69C>A | synonymous_variant | 0.22 |
panD | 4044225 | p.Asp19Glu | missense_variant | 0.15 |
embC | 4240822 | c.960C>A | synonymous_variant | 0.15 |
embC | 4240826 | p.Ala322Ser | missense_variant | 0.15 |
embC | 4240868 | p.His336Asn | missense_variant | 0.22 |
embC | 4240941 | p.Ser360Ile | missense_variant | 0.18 |
embA | 4242751 | c.-482G>T | upstream_gene_variant | 0.25 |
embA | 4243373 | p.Gln47His | missense_variant | 0.2 |
embA | 4243471 | p.Ala80Asp | missense_variant | 0.25 |
embA | 4243568 | c.336C>T | synonymous_variant | 0.29 |
embA | 4243721 | c.489G>T | synonymous_variant | 0.22 |
embA | 4244083 | p.Ala284Asp | missense_variant | 0.22 |
embA | 4245280 | p.Arg683Leu | missense_variant | 0.13 |
embA | 4246411 | c.3181delC | frameshift_variant | 0.33 |
embA | 4246483 | p.Trp1084Leu | missense_variant | 0.22 |
embB | 4246623 | p.Gly37Val | missense_variant | 0.17 |
embB | 4246762 | c.249G>T | synonymous_variant | 0.14 |
embB | 4247183 | p.Gly224Trp | missense_variant | 0.18 |
embB | 4248469 | p.Tyr652* | stop_gained | 0.15 |
embB | 4249594 | c.3081G>A | synonymous_variant | 0.13 |
embB | 4249625 | p.Gly1038Trp | missense_variant | 0.14 |
aftB | 4267882 | p.Gly319Ser | missense_variant | 0.15 |
aftB | 4268064 | p.Ser258* | stop_gained | 0.2 |
aftB | 4268440 | p.Asp133His | missense_variant | 0.2 |
aftB | 4268481 | p.Pro119Leu | missense_variant | 0.2 |
aftB | 4268630 | c.207G>T | synonymous_variant | 0.29 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.33 |
aftB | 4269459 | c.-623G>T | upstream_gene_variant | 0.15 |
ubiA | 4269634 | p.Ser67* | stop_gained | 0.22 |
ethA | 4326068 | p.Arg469Leu | missense_variant | 0.15 |
ethA | 4326167 | p.Pro436Gln | missense_variant | 0.2 |
ethA | 4326325 | c.1149G>T | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.32 |
whiB6 | 4338648 | c.-127A>T | upstream_gene_variant | 0.17 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.12 |
gid | 4408357 | c.-155C>A | upstream_gene_variant | 0.15 |