Run ID: SRR6832787
Sample name:
Date: 04-04-2023 17:38:48
Number of reads: 1536226
Percentage reads mapped: 71.78
Strain: lineage2.2.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.97 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.96 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761135 | p.Leu443Phe | missense_variant | 0.24 | rifampicin |
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5254 | c.15A>G | synonymous_variant | 0.22 |
gyrB | 5284 | c.45G>A | synonymous_variant | 0.29 |
gyrB | 5287 | c.48T>C | synonymous_variant | 0.3 |
gyrB | 5293 | c.54C>G | synonymous_variant | 0.33 |
gyrB | 5302 | c.63A>G | synonymous_variant | 0.38 |
gyrB | 5305 | c.66G>A | synonymous_variant | 0.4 |
gyrB | 5308 | c.69G>A | synonymous_variant | 0.4 |
gyrB | 5341 | c.102T>C | synonymous_variant | 0.35 |
gyrB | 5359 | c.120C>T | synonymous_variant | 0.25 |
gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 0.25 |
gyrB | 5377 | c.138T>C | synonymous_variant | 0.34 |
gyrB | 5422 | c.183T>C | synonymous_variant | 0.21 |
gyrB | 5425 | c.186A>G | synonymous_variant | 0.21 |
gyrB | 5426 | p.Thr63Ala | missense_variant | 0.21 |
gyrB | 5431 | c.192A>C | synonymous_variant | 0.21 |
gyrB | 5434 | c.195G>A | synonymous_variant | 0.2 |
gyrB | 5436 | p.Asn66Ser | missense_variant | 0.19 |
gyrB | 5440 | c.201A>G | synonymous_variant | 0.19 |
gyrB | 5449 | c.210T>C | synonymous_variant | 0.26 |
gyrB | 5455 | c.216T>C | synonymous_variant | 0.25 |
gyrB | 5470 | c.231C>G | synonymous_variant | 0.29 |
gyrB | 5485 | c.246C>T | synonymous_variant | 0.24 |
gyrB | 5488 | c.249C>A | synonymous_variant | 0.19 |
gyrB | 5491 | c.252T>C | synonymous_variant | 0.18 |
gyrB | 5500 | c.261C>A | synonymous_variant | 0.27 |
gyrB | 5502 | p.Thr88Met | missense_variant | 0.22 |
gyrB | 5527 | c.288C>G | synonymous_variant | 0.2 |
gyrB | 5542 | c.303A>C | synonymous_variant | 0.2 |
gyrB | 5545 | c.306A>G | synonymous_variant | 0.19 |
gyrB | 5548 | c.309A>G | synonymous_variant | 0.17 |
gyrB | 5551 | c.312T>C | synonymous_variant | 0.17 |
gyrB | 5560 | c.321C>G | synonymous_variant | 0.2 |
gyrB | 5569 | c.330C>T | synonymous_variant | 0.19 |
gyrB | 5836 | c.597C>T | synonymous_variant | 0.19 |
gyrB | 5851 | c.612G>C | synonymous_variant | 0.21 |
gyrB | 5860 | c.621C>T | synonymous_variant | 0.18 |
gyrB | 5869 | c.630C>T | synonymous_variant | 0.18 |
gyrB | 5870 | p.Glu211Gln | missense_variant | 0.18 |
gyrB | 5873 | c.634A>C | synonymous_variant | 0.18 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.17 |
gyrB | 6121 | c.882C>T | synonymous_variant | 0.17 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.16 |
gyrB | 6145 | c.906C>T | synonymous_variant | 0.18 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.25 |
gyrB | 6181 | c.942C>G | synonymous_variant | 0.26 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.29 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.34 |
gyrB | 6247 | c.1008G>A | synonymous_variant | 0.22 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.26 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.25 |
gyrB | 6259 | p.Asp340Glu | missense_variant | 0.24 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.32 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.3 |
gyrB | 6298 | c.1059C>G | synonymous_variant | 0.28 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.3 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.26 |
gyrA | 6313 | c.-989C>T | upstream_gene_variant | 0.24 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.26 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.24 |
gyrA | 6358 | c.-944C>G | upstream_gene_variant | 0.22 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.27 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.27 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.17 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.17 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.17 |
gyrA | 6826 | c.-476G>C | upstream_gene_variant | 0.24 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.2 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.2 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.19 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.18 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.22 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.17 |
gyrA | 6866 | c.-436C>T | upstream_gene_variant | 0.17 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.15 |
gyrA | 6886 | c.-416C>T | upstream_gene_variant | 0.16 |
gyrA | 6889 | c.-413G>C | upstream_gene_variant | 0.17 |
gyrA | 6898 | c.-404G>T | upstream_gene_variant | 0.17 |
gyrA | 7120 | c.-182T>C | upstream_gene_variant | 0.25 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.25 |
gyrA | 7129 | c.-173T>G | upstream_gene_variant | 0.29 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.27 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.33 |
gyrA | 7147 | c.-155G>C | upstream_gene_variant | 0.31 |
gyrA | 7151 | c.-151C>T | upstream_gene_variant | 0.31 |
gyrA | 7165 | c.-137C>A | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.15 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.14 |
gyrA | 7766 | c.465C>T | synonymous_variant | 0.19 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.19 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.18 |
gyrA | 7787 | c.486G>A | synonymous_variant | 0.19 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.16 |
gyrA | 7997 | c.696A>G | synonymous_variant | 0.17 |
gyrA | 8000 | c.699G>C | synonymous_variant | 0.19 |
gyrA | 8020 | p.Thr240Ile | missense_variant | 0.19 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.2 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.19 |
gyrA | 8084 | c.783G>A | synonymous_variant | 0.18 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.19 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.18 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.17 |
gyrA | 8105 | c.804G>T | synonymous_variant | 0.18 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.19 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.19 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.18 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.17 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.15 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.15 |
gyrA | 8447 | c.1146C>A | synonymous_variant | 0.2 |
gyrA | 8450 | c.1149G>A | synonymous_variant | 0.2 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.21 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.19 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.21 |
gyrA | 8510 | c.1209G>A | synonymous_variant | 0.29 |
gyrA | 8513 | c.1212C>G | synonymous_variant | 0.29 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.29 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.3 |
gyrA | 8531 | c.1230G>A | synonymous_variant | 0.39 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.32 |
gyrA | 8561 | c.1260A>G | synonymous_variant | 0.33 |
gyrA | 8562 | c.1261C>T | synonymous_variant | 0.33 |
gyrA | 8571 | c.1270C>T | synonymous_variant | 0.45 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.38 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.42 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.42 |
gyrA | 8627 | c.1326C>T | synonymous_variant | 0.36 |
gyrA | 8633 | c.1332C>G | synonymous_variant | 0.42 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.42 |
gyrA | 8655 | p.Ile452Val | missense_variant | 0.42 |
gyrA | 8666 | c.1365G>C | synonymous_variant | 0.44 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.4 |
gyrA | 8694 | c.1393C>T | synonymous_variant | 0.4 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.38 |
gyrA | 8723 | c.1422G>A | synonymous_variant | 0.36 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.33 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.33 |
gyrA | 8752 | p.Ala484Gly | missense_variant | 0.33 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.44 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.44 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.43 |
gyrA | 8783 | c.1482G>T | synonymous_variant | 0.35 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.35 |
gyrA | 8795 | c.1494C>T | synonymous_variant | 0.29 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.27 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.26 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.28 |
gyrA | 8813 | c.1512C>T | synonymous_variant | 0.27 |
gyrA | 8825 | c.1524G>A | synonymous_variant | 0.24 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.22 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.23 |
gyrA | 8852 | c.1551T>G | synonymous_variant | 0.26 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.15 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.25 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.28 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.29 |
gyrA | 8924 | c.1623C>G | synonymous_variant | 0.34 |
gyrA | 8933 | c.1632G>A | synonymous_variant | 0.36 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.28 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.26 |
gyrA | 8945 | c.1644G>T | synonymous_variant | 0.25 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.25 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.34 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.34 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.37 |
gyrA | 9003 | c.1702C>T | synonymous_variant | 0.39 |
gyrA | 9017 | c.1716C>T | synonymous_variant | 0.39 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.37 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.36 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.42 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.4 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.38 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.41 |
gyrA | 9080 | c.1779G>C | synonymous_variant | 0.38 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.34 |
gyrA | 9101 | c.1800A>G | synonymous_variant | 0.26 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.15 |
gyrA | 9197 | c.1896G>C | synonymous_variant | 0.21 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.2 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.32 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.34 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.45 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.48 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.55 |
gyrA | 9257 | c.1956C>T | synonymous_variant | 0.55 |
gyrA | 9284 | c.1983T>G | synonymous_variant | 0.5 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.32 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9315 | c.2014C>T | synonymous_variant | 0.28 |
gyrA | 9323 | c.2022C>T | synonymous_variant | 0.31 |
gyrA | 9341 | c.2040C>G | synonymous_variant | 0.32 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.29 |
gyrA | 9371 | c.2070G>A | synonymous_variant | 0.28 |
gyrA | 9374 | c.2073G>C | synonymous_variant | 0.3 |
gyrA | 9377 | c.2076A>G | synonymous_variant | 0.32 |
gyrA | 9383 | c.2082T>C | synonymous_variant | 0.28 |
gyrA | 9386 | c.2085T>G | synonymous_variant | 0.3 |
gyrA | 9395 | c.2094G>C | synonymous_variant | 0.34 |
gyrA | 9398 | c.2097T>G | synonymous_variant | 0.38 |
gyrA | 9401 | c.2100G>A | synonymous_variant | 0.4 |
gyrA | 9413 | c.2112G>A | synonymous_variant | 0.27 |
gyrA | 9419 | c.2118T>C | synonymous_variant | 0.25 |
gyrA | 9420 | p.Ile707Ala | missense_variant | 0.25 |
gyrA | 9449 | c.2148C>G | synonymous_variant | 0.22 |
gyrA | 9452 | c.2151G>C | synonymous_variant | 0.19 |
gyrA | 9476 | c.2175G>C | synonymous_variant | 0.16 |
gyrA | 9488 | c.2187G>C | synonymous_variant | 0.15 |
gyrA | 9494 | c.2193T>C | synonymous_variant | 0.16 |
gyrA | 9497 | c.2196G>C | synonymous_variant | 0.15 |
gyrA | 9527 | c.2226A>G | synonymous_variant | 0.17 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.19 |
fgd1 | 490809 | c.27A>G | synonymous_variant | 0.29 |
fgd1 | 490818 | c.36C>T | synonymous_variant | 0.35 |
fgd1 | 490830 | c.48A>C | synonymous_variant | 0.3 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.39 |
fgd1 | 490853 | p.Ala24Gly | missense_variant | 0.39 |
fgd1 | 490863 | c.81C>A | synonymous_variant | 0.43 |
fgd1 | 490869 | c.87C>T | synonymous_variant | 0.41 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.41 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.42 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.31 |
fgd1 | 490911 | c.129T>C | synonymous_variant | 0.31 |
fgd1 | 490921 | p.Gln47Lys | missense_variant | 0.28 |
fgd1 | 490929 | c.147C>G | synonymous_variant | 0.24 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.25 |
fgd1 | 490935 | c.153C>G | synonymous_variant | 0.26 |
fgd1 | 490945 | c.163C>T | synonymous_variant | 0.23 |
fgd1 | 490962 | c.180T>C | synonymous_variant | 0.16 |
fgd1 | 490971 | c.189A>G | synonymous_variant | 0.16 |
fgd1 | 490974 | c.192T>C | synonymous_variant | 0.19 |
fgd1 | 490980 | p.Asn66Lys | missense_variant | 0.17 |
fgd1 | 490984 | p.Leu68Val | missense_variant | 0.17 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.19 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.21 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.24 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.21 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.18 |
fgd1 | 491067 | c.285C>T | synonymous_variant | 0.15 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.18 |
fgd1 | 491085 | c.303T>G | synonymous_variant | 0.19 |
fgd1 | 491091 | c.309T>G | synonymous_variant | 0.19 |
fgd1 | 491094 | c.312C>T | synonymous_variant | 0.16 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.2 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.21 |
fgd1 | 491142 | c.360C>G | synonymous_variant | 0.19 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.16 |
fgd1 | 491154 | p.Glu124Asp | missense_variant | 0.16 |
fgd1 | 491163 | c.381G>A | synonymous_variant | 0.15 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.18 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.16 |
fgd1 | 491512 | p.Asn244His | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575561 | p.Met72Val | missense_variant | 0.16 |
mshA | 575629 | c.282A>T | synonymous_variant | 0.18 |
mshA | 575633 | p.Ala96Thr | missense_variant | 0.18 |
mshA | 575652 | p.Arg102Gln | missense_variant | 0.2 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.24 |
mshA | 575662 | c.315C>A | synonymous_variant | 0.22 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.25 |
mshA | 575686 | c.339G>A | synonymous_variant | 0.3 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.38 |
mshA | 575692 | c.345G>A | synonymous_variant | 0.39 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.36 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.35 |
mshA | 575732 | c.385_387delCTTinsTTG | synonymous_variant | 0.32 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.31 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.33 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.31 |
mshA | 575770 | c.423G>C | synonymous_variant | 0.32 |
mshA | 575772 | p.Val142Ala | missense_variant | 0.32 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.32 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.23 |
mshA | 575824 | c.477T>C | synonymous_variant | 0.17 |
mshA | 575842 | c.495G>C | synonymous_variant | 0.22 |
mshA | 575848 | c.501C>T | synonymous_variant | 0.24 |
mshA | 575872 | c.525C>T | synonymous_variant | 0.17 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.15 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.88 |
mshA | 576230 | p.Ile295Val | missense_variant | 0.16 |
mshA | 576233 | p.Ile296Val | missense_variant | 0.18 |
mshA | 576238 | c.891G>C | synonymous_variant | 0.2 |
mshA | 576247 | c.900A>G | synonymous_variant | 0.21 |
mshA | 576259 | c.912C>T | synonymous_variant | 0.18 |
mshA | 576262 | c.915T>A | synonymous_variant | 0.18 |
ccsA | 620337 | c.447C>G | synonymous_variant | 0.14 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.16 |
ccsA | 620358 | c.468C>G | synonymous_variant | 0.15 |
ccsA | 620397 | c.507C>G | synonymous_variant | 0.18 |
ccsA | 620404 | c.514C>T | synonymous_variant | 0.19 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.18 |
ccsA | 620604 | c.714C>G | synonymous_variant | 0.19 |
ccsA | 620607 | c.717T>G | synonymous_variant | 0.17 |
ccsA | 620613 | c.723C>T | synonymous_variant | 0.18 |
ccsA | 620619 | c.729G>A | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620631 | c.741T>G | synonymous_variant | 0.16 |
ccsA | 620829 | c.939G>T | synonymous_variant | 0.16 |
rpoB | 759635 | c.-172C>T | upstream_gene_variant | 0.23 |
rpoB | 759644 | c.-163T>A | upstream_gene_variant | 0.32 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.29 |
rpoB | 759661 | c.-146G>C | upstream_gene_variant | 0.39 |
rpoB | 759670 | c.-137C>T | upstream_gene_variant | 0.3 |
rpoB | 759671 | c.-136G>T | upstream_gene_variant | 0.29 |
rpoB | 759675 | c.-132T>C | upstream_gene_variant | 0.29 |
rpoB | 759676 | c.-131A>G | upstream_gene_variant | 0.29 |
rpoB | 759701 | c.-106A>T | upstream_gene_variant | 0.25 |
rpoB | 759725 | c.-82A>C | upstream_gene_variant | 0.2 |
rpoB | 759732 | c.-75_-74insT | upstream_gene_variant | 0.14 |
rpoB | 759899 | c.93C>T | synonymous_variant | 0.14 |
rpoB | 759944 | c.138A>G | synonymous_variant | 0.17 |
rpoB | 759945 | c.139_141delCTCinsTTG | synonymous_variant | 0.17 |
rpoB | 760067 | c.261G>C | synonymous_variant | 0.17 |
rpoB | 760070 | c.264T>A | synonymous_variant | 0.17 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.21 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.21 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.2 |
rpoB | 760118 | c.312T>C | synonymous_variant | 0.22 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.24 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.23 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.21 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.25 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.26 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.29 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.3 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.32 |
rpoB | 760343 | c.537G>C | synonymous_variant | 0.32 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.32 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.4 |
rpoB | 760409 | c.603C>T | synonymous_variant | 0.33 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.33 |
rpoB | 760415 | c.609C>G | synonymous_variant | 0.33 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.33 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.3 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.28 |
rpoB | 760445 | c.639C>T | synonymous_variant | 0.24 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.25 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.27 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.32 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.3 |
rpoB | 760528 | p.Gln241Arg | missense_variant | 0.29 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.3 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.3 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.29 |
rpoB | 760577 | c.771G>A | synonymous_variant | 0.27 |
rpoB | 760625 | c.819C>A | synonymous_variant | 0.16 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.16 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.17 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.19 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.17 |
rpoB | 760673 | c.867G>A | synonymous_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.16 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.17 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.18 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.18 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.21 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.24 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.23 |
rpoB | 760859 | c.1053T>G | synonymous_variant | 0.25 |
rpoB | 760868 | c.1062C>G | synonymous_variant | 0.26 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.32 |
rpoB | 760920 | c.1114C>T | synonymous_variant | 0.32 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.31 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.34 |
rpoB | 760971 | c.1165C>A | synonymous_variant | 0.36 |
rpoB | 760994 | c.1188G>A | synonymous_variant | 0.47 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.44 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.3 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.31 |
rpoB | 761036 | c.1230G>A | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.29 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.33 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.31 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.24 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.24 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.24 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>G | synonymous_variant | 0.22 |
rpoB | 761153 | c.1347G>T | synonymous_variant | 0.24 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.26 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.22 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.22 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.26 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.22 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.22 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.24 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.27 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.22 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.21 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.21 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.14 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.17 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.16 |
rpoB | 761471 | c.1665C>G | synonymous_variant | 0.2 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.19 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.21 |
rpoB | 761502 | p.Pro566Ala | missense_variant | 0.16 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.22 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.17 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.19 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.19 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.2 |
rpoB | 761600 | c.1794T>G | synonymous_variant | 0.2 |
rpoB | 761603 | c.1797C>T | synonymous_variant | 0.19 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.19 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.19 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.14 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.15 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.19 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.29 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.32 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.31 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.3 |
rpoB | 762020 | c.2214G>A | synonymous_variant | 0.31 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.29 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.28 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.32 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.32 |
rpoB | 762071 | c.2265C>T | synonymous_variant | 0.32 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.24 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.24 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.36 |
rpoB | 762119 | c.2313C>T | synonymous_variant | 0.44 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.39 |
rpoB | 762134 | c.2328C>G | synonymous_variant | 0.39 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.39 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.36 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.16 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.13 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.19 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.15 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.17 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.22 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.24 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.24 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.16 |
rpoB | 762486 | p.Pro894Ala | missense_variant | 0.17 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.17 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.17 |
rpoC | 762518 | c.-852C>G | upstream_gene_variant | 0.17 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.14 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.15 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.15 |
rpoC | 762776 | c.-594C>T | upstream_gene_variant | 0.16 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.17 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.27 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.21 |
rpoB | 762813 | p.Met1003Val | missense_variant | 0.21 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.19 |
rpoC | 762830 | c.-540C>T | upstream_gene_variant | 0.18 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.19 |
rpoC | 762860 | c.-510G>T | upstream_gene_variant | 0.19 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.23 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.29 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.3 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.26 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.31 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 0.43 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.42 |
rpoC | 763076 | c.-294C>T | upstream_gene_variant | 0.43 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.43 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.42 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.4 |
rpoC | 763124 | c.-246C>T | upstream_gene_variant | 0.37 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.36 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.21 |
rpoC | 763375 | c.6C>A | synonymous_variant | 0.17 |
rpoC | 763408 | c.39T>C | synonymous_variant | 0.19 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.19 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.18 |
rpoC | 763430 | c.61A>C | synonymous_variant | 0.29 |
rpoC | 763435 | c.66A>G | synonymous_variant | 0.28 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.33 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.57 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.75 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.68 |
rpoC | 763505 | c.136C>T | synonymous_variant | 0.55 |
rpoC | 763561 | c.192G>A | synonymous_variant | 0.27 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.16 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763636 | c.267T>G | synonymous_variant | 0.21 |
rpoC | 763639 | c.270G>A | synonymous_variant | 0.2 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.18 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.33 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.32 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.32 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.31 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.33 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.35 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.27 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.26 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.29 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.29 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.32 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.28 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.24 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.22 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.21 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.21 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.19 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.24 |
rpoC | 763948 | c.579G>C | synonymous_variant | 0.24 |
rpoC | 763951 | c.582G>A | synonymous_variant | 0.24 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.21 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.14 |
rpoC | 764119 | c.750G>A | synonymous_variant | 0.2 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.27 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.31 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.4 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.42 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.44 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.43 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.48 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.48 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.48 |
rpoC | 764272 | c.903G>T | synonymous_variant | 0.48 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.52 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.52 |
rpoC | 764317 | c.948C>T | synonymous_variant | 0.43 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.31 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.29 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.23 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.17 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.17 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.16 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.16 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.16 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.19 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.19 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.2 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.21 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.29 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.39 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.33 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.33 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.36 |
rpoC | 764524 | c.1155C>A | synonymous_variant | 0.35 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.35 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.38 |
rpoC | 764536 | c.1167G>A | synonymous_variant | 0.36 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.36 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.36 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.36 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.32 |
rpoC | 764648 | c.1279C>A | synonymous_variant | 0.38 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.41 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.43 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.37 |
rpoC | 764674 | c.1305G>A | synonymous_variant | 0.43 |
rpoC | 764681 | c.1312C>T | synonymous_variant | 0.44 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.43 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.37 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.36 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.35 |
rpoC | 764767 | c.1398G>C | synonymous_variant | 0.33 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.28 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.23 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.22 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.23 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.21 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.22 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.26 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.22 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.21 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.21 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.22 |
rpoC | 764918 | p.Val517Ile | missense_variant | 0.19 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.18 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.19 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.17 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.17 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.16 |
rpoC | 765752 | p.Asp795Asn | missense_variant | 0.14 |
rpoC | 765757 | c.2388C>T | synonymous_variant | 0.17 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.19 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.19 |
rpoC | 765790 | c.2421C>T | synonymous_variant | 0.19 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.21 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.19 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.17 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.18 |
rpoC | 765826 | c.2457T>A | synonymous_variant | 0.22 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.26 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.23 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.2 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.19 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.19 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.21 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.17 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.2 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.18 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.18 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.16 |
rpoC | 765997 | c.2628T>C | synonymous_variant | 0.16 |
rpoC | 766255 | c.2886G>T | synonymous_variant | 0.15 |
rpoC | 766270 | c.2901G>C | synonymous_variant | 0.22 |
rpoC | 766274 | p.Ala969Thr | missense_variant | 0.21 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 0.24 |
rpoC | 766300 | c.2931C>G | synonymous_variant | 0.31 |
rpoC | 766303 | c.2934C>T | synonymous_variant | 0.31 |
rpoC | 766306 | c.2937C>T | synonymous_variant | 0.3 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.31 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.3 |
rpoC | 766324 | c.2955C>T | synonymous_variant | 0.35 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.4 |
rpoC | 766360 | c.2991C>T | synonymous_variant | 0.37 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.39 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.39 |
rpoC | 766387 | c.3018C>G | synonymous_variant | 0.38 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.31 |
rpoC | 766397 | c.3028C>T | synonymous_variant | 0.31 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.34 |
rpoC | 766417 | c.3048C>T | synonymous_variant | 0.34 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.35 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.22 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.23 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.22 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.22 |
rpoC | 766519 | c.3150C>A | synonymous_variant | 0.22 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.17 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.21 |
rpoC | 766537 | c.3168G>A | synonymous_variant | 0.21 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.21 |
rpoC | 766549 | c.3180G>T | synonymous_variant | 0.19 |
rpoC | 766570 | c.3201T>G | synonymous_variant | 0.15 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.15 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.17 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.17 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.21 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.23 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.17 |
rpoC | 766621 | c.3252G>A | synonymous_variant | 0.16 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.16 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.16 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.22 |
rpoC | 766795 | c.3426C>T | synonymous_variant | 0.24 |
rpoC | 766801 | c.3432C>T | synonymous_variant | 0.27 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.28 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.26 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.24 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.22 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.17 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.17 |
rpoC | 766907 | c.3538C>T | synonymous_variant | 0.16 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.21 |
rpoC | 766921 | c.3552G>C | synonymous_variant | 0.2 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.24 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.19 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.17 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.3 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.32 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.25 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.29 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.33 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.3 |
rpoC | 767185 | c.3816G>T | synonymous_variant | 0.32 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.31 |
rpoC | 767200 | c.3831G>A | synonymous_variant | 0.29 |
rpoC | 767206 | c.3837C>A | synonymous_variant | 0.21 |
rpoC | 767209 | c.3840T>G | synonymous_variant | 0.21 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.2 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.25 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.23 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.97 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.97 |
rpsL | 781586 | c.27C>A | synonymous_variant | 0.16 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.19 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.24 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.24 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.3 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.24 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.2 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.22 |
rpsL | 781667 | c.108C>G | synonymous_variant | 0.23 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.2 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.22 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.22 |
rpsL | 781721 | c.162C>G | synonymous_variant | 0.22 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.19 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.16 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.2 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.18 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.22 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.21 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.16 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.15 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.21 |
rplC | 800797 | c.-12T>G | upstream_gene_variant | 0.16 |
rplC | 800799 | c.-10G>C | upstream_gene_variant | 0.16 |
rplC | 800800 | c.-9G>T | upstream_gene_variant | 0.16 |
rplC | 800801 | c.-8A>G | upstream_gene_variant | 0.16 |
rplC | 800817 | c.9A>C | synonymous_variant | 0.21 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.24 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.3 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.29 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.3 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.29 |
rplC | 800913 | c.105G>C | synonymous_variant | 0.28 |
rplC | 800916 | c.108A>T | synonymous_variant | 0.28 |
rplC | 800922 | c.114C>G | synonymous_variant | 0.26 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.23 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.23 |
rplC | 800946 | c.138T>G | synonymous_variant | 0.23 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.23 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.21 |
rplC | 800958 | c.150G>A | synonymous_variant | 0.21 |
rplC | 801201 | c.393C>T | synonymous_variant | 0.19 |
rplC | 801210 | c.402T>C | synonymous_variant | 0.18 |
rplC | 801216 | c.408C>A | synonymous_variant | 0.18 |
rplC | 801219 | c.411C>T | synonymous_variant | 0.19 |
rplC | 801220 | p.Ser138Ala | missense_variant | 0.19 |
rplC | 801246 | c.438C>G | synonymous_variant | 0.33 |
rplC | 801252 | c.444G>C | synonymous_variant | 0.3 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.27 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.28 |
rplC | 801297 | c.489C>T | synonymous_variant | 0.24 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.24 |
fbiC | 1303681 | c.751_753delTTGinsCTC | synonymous_variant | 0.18 |
fbiC | 1303689 | c.759T>C | synonymous_variant | 0.18 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.17 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 0.15 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.17 |
fbiC | 1304163 | c.1233G>C | synonymous_variant | 0.19 |
fbiC | 1304164 | p.Gly412Arg | missense_variant | 0.18 |
fbiC | 1304172 | c.1242G>T | synonymous_variant | 0.15 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.16 |
fbiC | 1304178 | c.1248G>C | synonymous_variant | 0.17 |
fbiC | 1304181 | c.1251G>T | synonymous_variant | 0.17 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.18 |
fbiC | 1304202 | c.1272G>C | synonymous_variant | 0.17 |
fbiC | 1304205 | c.1275C>G | synonymous_variant | 0.17 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.18 |
fbiC | 1304217 | p.Asn429Lys | missense_variant | 0.16 |
fbiC | 1304546 | p.Val539Ala | missense_variant | 0.24 |
fbiC | 1304556 | c.1626C>T | synonymous_variant | 0.18 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.19 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.27 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.23 |
fbiC | 1304598 | c.1668C>T | synonymous_variant | 0.24 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.24 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.26 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.21 |
fbiC | 1304649 | c.1719C>T | synonymous_variant | 0.23 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.2 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.2 |
fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.15 |
fbiC | 1304679 | c.1749G>A | synonymous_variant | 0.17 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.16 |
fbiC | 1304703 | c.1773C>T | synonymous_variant | 0.15 |
fbiC | 1304715 | c.1785G>T | synonymous_variant | 0.18 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.15 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.16 |
fbiC | 1304751 | c.1821C>G | synonymous_variant | 0.19 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.2 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.19 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416850 | c.498G>C | synonymous_variant | 0.17 |
embR | 1416856 | c.492G>C | synonymous_variant | 0.18 |
embR | 1416862 | c.486T>C | synonymous_variant | 0.18 |
embR | 1416865 | p.Pro161Ala | missense_variant | 0.18 |
embR | 1416868 | p.Glu160Asn | missense_variant | 0.19 |
atpE | 1461185 | c.141G>A | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471984 | n.139T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472040 | n.195T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473541 | n.-117G>A | upstream_gene_variant | 0.19 |
rrl | 1473542 | n.-116C>T | upstream_gene_variant | 0.19 |
rrl | 1473571 | n.-87C>T | upstream_gene_variant | 0.29 |
rrl | 1473635 | n.-23_-22insTTT | upstream_gene_variant | 0.2 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474950 | n.1293G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475369 | n.1712G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.35 |
inhA | 1673493 | c.-709C>T | upstream_gene_variant | 0.17 |
inhA | 1673499 | c.-703T>C | upstream_gene_variant | 0.17 |
inhA | 1673505 | c.-697A>T | upstream_gene_variant | 0.18 |
inhA | 1673517 | c.-685G>A | upstream_gene_variant | 0.19 |
inhA | 1673535 | c.-667A>G | upstream_gene_variant | 0.16 |
inhA | 1673568 | c.-634C>G | upstream_gene_variant | 0.16 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.14 |
inhA | 1673664 | c.-538A>C | upstream_gene_variant | 0.2 |
inhA | 1673667 | c.-535A>G | upstream_gene_variant | 0.2 |
inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.28 |
inhA | 1673682 | c.-520G>C | upstream_gene_variant | 0.28 |
inhA | 1673685 | c.-517C>T | upstream_gene_variant | 0.26 |
fabG1 | 1673710 | p.Leu91Val | missense_variant | 0.24 |
inhA | 1673715 | c.-487C>T | upstream_gene_variant | 0.23 |
inhA | 1673724 | c.-478A>G | upstream_gene_variant | 0.24 |
inhA | 1673730 | c.-472C>G | upstream_gene_variant | 0.24 |
fabG1 | 1673733 | p.Met98Ile | missense_variant | 0.22 |
inhA | 1673736 | c.-466G>A | upstream_gene_variant | 0.22 |
inhA | 1673745 | c.-457G>A | upstream_gene_variant | 0.21 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.21 |
fabG1 | 1673749 | p.Lys104Arg | missense_variant | 0.21 |
fabG1 | 1673767 | p.Asn110Asp | missense_variant | 0.15 |
inhA | 1673916 | c.-286A>T | upstream_gene_variant | 0.21 |
inhA | 1673919 | c.-283G>C | upstream_gene_variant | 0.19 |
inhA | 1673922 | c.-280T>C | upstream_gene_variant | 0.19 |
inhA | 1673925 | c.-277C>G | upstream_gene_variant | 0.21 |
inhA | 1673946 | c.-256C>A | upstream_gene_variant | 0.17 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.16 |
fabG1 | 1673960 | p.Ala174Val | missense_variant | 0.17 |
inhA | 1673970 | c.-232C>G | upstream_gene_variant | 0.16 |
inhA | 1673976 | c.-226T>C | upstream_gene_variant | 0.16 |
inhA | 1673982 | c.-220G>C | upstream_gene_variant | 0.18 |
inhA | 1673988 | c.-214G>C | upstream_gene_variant | 0.18 |
inhA | 1673991 | c.-211C>G | upstream_gene_variant | 0.21 |
inhA | 1674015 | c.-187C>A | upstream_gene_variant | 0.2 |
inhA | 1674018 | c.-184G>C | upstream_gene_variant | 0.21 |
inhA | 1674024 | c.-178T>C | upstream_gene_variant | 0.17 |
inhA | 1674033 | c.-169T>C | upstream_gene_variant | 0.16 |
inhA | 1674045 | c.-157G>A | upstream_gene_variant | 0.17 |
inhA | 1674054 | c.-148T>C | upstream_gene_variant | 0.15 |
inhA | 1674060 | c.-142A>G | upstream_gene_variant | 0.16 |
inhA | 1674675 | c.474C>T | synonymous_variant | 0.2 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.18 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.21 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.27 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.2 |
inhA | 1674762 | c.561T>C | synonymous_variant | 0.21 |
inhA | 1674774 | c.573A>C | synonymous_variant | 0.21 |
inhA | 1674777 | c.576C>G | synonymous_variant | 0.19 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.18 |
inhA | 1674799 | p.Ser200Gly | missense_variant | 0.15 |
inhA | 1674822 | c.621C>G | synonymous_variant | 0.16 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.14 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.14 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.4 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.47 |
rpsA | 1833593 | p.Ser18Thr | missense_variant | 0.47 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.5 |
rpsA | 1833610 | c.69C>A | synonymous_variant | 0.5 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.41 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 0.43 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.31 |
rpsA | 1833718 | c.177C>T | synonymous_variant | 0.36 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.38 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.38 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.37 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.38 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.4 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.41 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.39 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.37 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.38 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.45 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.41 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.3 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.31 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.38 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.5 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.5 |
rpsA | 1834024 | c.483G>A | synonymous_variant | 0.5 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.45 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.38 |
rpsA | 1834102 | c.561T>G | synonymous_variant | 0.16 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.19 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.15 |
rpsA | 1834154 | p.Asn205His | missense_variant | 0.15 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.16 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.17 |
rpsA | 1834174 | c.633C>T | synonymous_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.25 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.27 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.33 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.44 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.39 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.35 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.38 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.39 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.4 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.38 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.38 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.36 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.33 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.35 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.36 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.36 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.36 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.34 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.28 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.22 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.24 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.23 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.26 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.31 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.25 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.27 |
rpsA | 1834495 | c.954G>A | synonymous_variant | 0.26 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.38 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.32 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.2 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.16 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101732 | c.1311T>C | synonymous_variant | 0.15 |
ndh | 2101744 | p.Asp433Glu | missense_variant | 0.15 |
ndh | 2101765 | c.1278C>G | synonymous_variant | 0.17 |
ndh | 2101768 | c.1275C>G | synonymous_variant | 0.17 |
ndh | 2101774 | c.1269T>C | synonymous_variant | 0.17 |
ndh | 2101777 | c.1266C>G | synonymous_variant | 0.17 |
ndh | 2101783 | c.1260T>C | synonymous_variant | 0.17 |
ndh | 2101795 | c.1248G>C | synonymous_variant | 0.16 |
ndh | 2101804 | c.1239T>G | synonymous_variant | 0.14 |
ndh | 2101812 | p.Ile411Val | missense_variant | 0.14 |
ndh | 2101873 | c.1170T>C | synonymous_variant | 0.12 |
ndh | 2101899 | p.Ile382Val | missense_variant | 0.15 |
ndh | 2101912 | c.1131G>C | synonymous_variant | 0.18 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.18 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.17 |
ndh | 2101936 | c.1107G>C | synonymous_variant | 0.25 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.25 |
ndh | 2101960 | c.1083A>C | synonymous_variant | 0.21 |
ndh | 2101963 | c.1080G>A | synonymous_variant | 0.18 |
ndh | 2102247 | p.Val266Ile | missense_variant | 0.19 |
ndh | 2102263 | c.780G>A | synonymous_variant | 0.22 |
ndh | 2102287 | c.756C>A | synonymous_variant | 0.32 |
ndh | 2102302 | c.741G>C | synonymous_variant | 0.32 |
ndh | 2102317 | c.726A>G | synonymous_variant | 0.36 |
ndh | 2102328 | p.Leu239Met | missense_variant | 0.15 |
ndh | 2102989 | c.54G>C | synonymous_variant | 0.16 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168762 | c.1851A>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.21 |
kasA | 2517956 | c.-159G>A | upstream_gene_variant | 0.17 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.16 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.15 |
kasA | 2518034 | c.-81T>C | upstream_gene_variant | 0.15 |
kasA | 2518035 | c.-80C>G | upstream_gene_variant | 0.15 |
kasA | 2518041 | c.-74T>C | upstream_gene_variant | 0.14 |
kasA | 2518046 | c.-69C>G | upstream_gene_variant | 0.15 |
kasA | 2518049 | c.-66G>C | upstream_gene_variant | 0.15 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.26 |
kasA | 2518252 | c.138C>T | synonymous_variant | 0.26 |
kasA | 2518279 | c.165T>C | synonymous_variant | 0.28 |
kasA | 2518283 | p.Ala57Pro | missense_variant | 0.3 |
kasA | 2518297 | c.183C>T | synonymous_variant | 0.26 |
kasA | 2518300 | c.186T>C | synonymous_variant | 0.23 |
kasA | 2518312 | c.198T>C | synonymous_variant | 0.19 |
kasA | 2518318 | c.204C>G | synonymous_variant | 0.19 |
kasA | 2518323 | p.Ser70Asn | missense_variant | 0.15 |
kasA | 2518439 | p.Ala109Thr | missense_variant | 0.17 |
kasA | 2518459 | c.345T>C | synonymous_variant | 0.17 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.2 |
kasA | 2518468 | c.354A>G | synonymous_variant | 0.16 |
kasA | 2518471 | c.357C>G | synonymous_variant | 0.17 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.17 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.16 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.18 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.18 |
kasA | 2518513 | c.399C>G | synonymous_variant | 0.21 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.23 |
kasA | 2518534 | c.420G>C | synonymous_variant | 0.17 |
kasA | 2518537 | c.423C>G | synonymous_variant | 0.17 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.2 |
kasA | 2518567 | c.453G>T | synonymous_variant | 0.18 |
kasA | 2518573 | c.459G>C | synonymous_variant | 0.18 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.23 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.26 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.25 |
kasA | 2518618 | c.504G>C | synonymous_variant | 0.15 |
kasA | 2518633 | c.519G>C | synonymous_variant | 0.17 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.21 |
kasA | 2518645 | c.531G>C | synonymous_variant | 0.21 |
kasA | 2518648 | c.534C>T | synonymous_variant | 0.21 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.19 |
kasA | 2518681 | c.567C>T | synonymous_variant | 0.19 |
kasA | 2518684 | c.570C>A | synonymous_variant | 0.16 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.17 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.21 |
kasA | 2518735 | c.621C>A | synonymous_variant | 0.19 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.18 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.19 |
kasA | 2518756 | c.642G>C | synonymous_variant | 0.29 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.29 |
kasA | 2518789 | c.675G>T | synonymous_variant | 0.29 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.29 |
kasA | 2518798 | c.684G>C | synonymous_variant | 0.26 |
kasA | 2518816 | c.702C>T | synonymous_variant | 0.2 |
kasA | 2518822 | c.708C>T | synonymous_variant | 0.17 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.15 |
kasA | 2518856 | p.Ile248Leu | missense_variant | 0.15 |
kasA | 2518903 | c.789C>T | synonymous_variant | 0.18 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.17 |
kasA | 2518910 | c.796C>T | synonymous_variant | 0.19 |
kasA | 2518939 | c.825T>C | synonymous_variant | 0.14 |
kasA | 2518942 | c.828T>C | synonymous_variant | 0.14 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 0.21 |
ahpC | 2726354 | c.162G>C | synonymous_variant | 0.19 |
ahpC | 2726357 | c.165A>G | synonymous_variant | 0.19 |
ahpC | 2726366 | c.174G>C | synonymous_variant | 0.21 |
ahpC | 2726378 | c.186T>G | synonymous_variant | 0.21 |
ahpC | 2726393 | c.201G>C | synonymous_variant | 0.23 |
ahpC | 2726397 | p.Ser69Gly | missense_variant | 0.22 |
ahpC | 2726408 | c.216T>C | synonymous_variant | 0.24 |
ahpC | 2726430 | p.Ala80Thr | missense_variant | 0.23 |
ahpC | 2726441 | c.249G>C | synonymous_variant | 0.15 |
folC | 2747059 | c.540T>A | synonymous_variant | 0.17 |
folC | 2747065 | c.534C>T | synonymous_variant | 0.2 |
folC | 2747071 | c.528C>T | synonymous_variant | 0.19 |
folC | 2747086 | c.513A>C | synonymous_variant | 0.19 |
folC | 2747089 | c.510G>C | synonymous_variant | 0.18 |
folC | 2747230 | c.369C>G | synonymous_variant | 0.16 |
folC | 2747263 | c.336C>A | synonymous_variant | 0.19 |
folC | 2747275 | c.324T>C | synonymous_variant | 0.18 |
folC | 2747278 | c.321C>G | synonymous_variant | 0.19 |
folC | 2747288 | p.Pro104Val | missense_variant | 0.18 |
folC | 2747290 | c.309A>G | synonymous_variant | 0.18 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.18 |
folC | 2747442 | c.157T>C | synonymous_variant | 0.19 |
folC | 2747454 | c.145C>A | synonymous_variant | 0.19 |
folC | 2747467 | p.Asp44Glu | missense_variant | 0.2 |
folC | 2747491 | c.108A>G | synonymous_variant | 0.23 |
folC | 2747497 | c.102C>G | synonymous_variant | 0.23 |
folC | 2747500 | c.99A>G | synonymous_variant | 0.22 |
folC | 2747503 | c.96T>C | synonymous_variant | 0.23 |
folC | 2747509 | c.90T>C | synonymous_variant | 0.24 |
folC | 2747520 | c.79C>T | synonymous_variant | 0.21 |
folC | 2747521 | c.78C>G | synonymous_variant | 0.22 |
folC | 2747524 | c.75G>T | synonymous_variant | 0.22 |
folC | 2747539 | c.60T>A | synonymous_variant | 0.19 |
pepQ | 2859468 | c.951G>T | synonymous_variant | 0.27 |
pepQ | 2859489 | p.Val310Ala | missense_variant | 0.55 |
pepQ | 2859510 | c.909T>C | synonymous_variant | 0.53 |
pepQ | 2859528 | c.891T>C | synonymous_variant | 0.35 |
pepQ | 2859540 | c.879A>T | synonymous_variant | 0.26 |
pepQ | 2859546 | c.873T>C | synonymous_variant | 0.19 |
pepQ | 2859552 | p.His289Asn | missense_variant | 0.18 |
pepQ | 2859555 | p.Glu288Asp | missense_variant | 0.17 |
pepQ | 2859567 | c.852C>G | synonymous_variant | 0.15 |
pepQ | 2860236 | c.183C>T | synonymous_variant | 0.19 |
pepQ | 2860259 | c.160T>C | synonymous_variant | 0.19 |
pepQ | 2860263 | c.156C>G | synonymous_variant | 0.19 |
pepQ | 2860266 | p.Asp51Glu | missense_variant | 0.19 |
pepQ | 2860272 | c.147G>A | synonymous_variant | 0.21 |
pepQ | 2860275 | c.144T>C | synonymous_variant | 0.23 |
pepQ | 2860293 | c.126A>G | synonymous_variant | 0.19 |
pepQ | 2860314 | c.105C>T | synonymous_variant | 0.2 |
pepQ | 2860317 | c.102A>C | synonymous_variant | 0.19 |
pepQ | 2860397 | p.Asp8His | missense_variant | 0.17 |
pepQ | 2860423 | c.-5G>C | upstream_gene_variant | 0.19 |
pepQ | 2860447 | c.-29A>G | upstream_gene_variant | 0.21 |
pepQ | 2860448 | c.-30C>A | upstream_gene_variant | 0.21 |
pepQ | 2860475 | c.-57C>T | upstream_gene_variant | 0.18 |
pepQ | 2860476 | c.-58A>G | upstream_gene_variant | 0.19 |
pepQ | 2860480 | c.-62G>A | upstream_gene_variant | 0.2 |
Rv2752c | 3065217 | c.975C>T | synonymous_variant | 0.16 |
Rv2752c | 3065226 | c.966G>A | synonymous_variant | 0.19 |
Rv2752c | 3065229 | c.963G>C | synonymous_variant | 0.2 |
Rv2752c | 3065232 | c.960T>C | synonymous_variant | 0.22 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.22 |
Rv2752c | 3065244 | c.948G>T | synonymous_variant | 0.17 |
Rv2752c | 3065556 | c.636G>A | synonymous_variant | 0.17 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.15 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.16 |
Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 0.16 |
Rv2752c | 3065625 | c.567G>C | synonymous_variant | 0.18 |
Rv2752c | 3065634 | c.558G>C | synonymous_variant | 0.17 |
Rv2752c | 3065637 | c.555A>G | synonymous_variant | 0.17 |
Rv2752c | 3065640 | c.552T>C | synonymous_variant | 0.17 |
thyX | 3067247 | c.699C>A | synonymous_variant | 0.2 |
thyX | 3067250 | c.696G>C | synonymous_variant | 0.2 |
thyX | 3067277 | c.669C>A | synonymous_variant | 0.18 |
thyX | 3067280 | p.Val222Ser | missense_variant | 0.24 |
thyX | 3067284 | p.Ala221Asp | missense_variant | 0.25 |
thyX | 3067292 | c.654G>A | synonymous_variant | 0.17 |
thyX | 3067295 | c.651C>T | synonymous_variant | 0.21 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.29 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.3 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.31 |
thyX | 3067331 | c.615C>T | synonymous_variant | 0.29 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.29 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.24 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.21 |
thyX | 3067394 | c.552G>T | synonymous_variant | 0.21 |
thyX | 3067784 | c.162C>T | synonymous_variant | 0.14 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.15 |
thyX | 3067817 | c.129C>T | synonymous_variant | 0.16 |
thyX | 3067820 | c.126C>G | synonymous_variant | 0.15 |
thyX | 3067832 | c.114C>T | synonymous_variant | 0.14 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.23 |
thyA | 3073997 | c.475C>T | synonymous_variant | 0.25 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.27 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.29 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.31 |
thyA | 3074045 | c.427C>T | synonymous_variant | 0.3 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.29 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.29 |
thyA | 3074061 | p.Glu137Asp | missense_variant | 0.29 |
thyA | 3074091 | c.381C>G | synonymous_variant | 0.17 |
thyA | 3074297 | c.175C>T | synonymous_variant | 0.17 |
thyA | 3074313 | c.159A>G | synonymous_variant | 0.17 |
thyA | 3074334 | c.138T>C | synonymous_variant | 0.23 |
thyA | 3074349 | c.123T>C | synonymous_variant | 0.27 |
thyA | 3074355 | c.117G>C | synonymous_variant | 0.19 |
thyA | 3074360 | c.112T>C | synonymous_variant | 0.25 |
thyA | 3074361 | c.111T>C | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474138 | c.132T>G | synonymous_variant | 0.15 |
Rv3236c | 3612667 | c.450T>G | synonymous_variant | 0.15 |
Rv3236c | 3612805 | c.312T>C | synonymous_variant | 0.21 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.77 |
Rv3236c | 3612829 | c.288T>C | synonymous_variant | 0.21 |
Rv3236c | 3612835 | c.282T>C | synonymous_variant | 0.27 |
Rv3236c | 3612838 | c.279G>C | synonymous_variant | 0.25 |
Rv3236c | 3612850 | c.267C>T | synonymous_variant | 0.23 |
Rv3236c | 3612853 | c.264C>T | synonymous_variant | 0.2 |
Rv3236c | 3612856 | c.261C>T | synonymous_variant | 0.19 |
Rv3236c | 3612862 | c.255T>C | synonymous_variant | 0.19 |
Rv3236c | 3612883 | c.234T>C | synonymous_variant | 0.18 |
Rv3236c | 3612886 | c.231T>C | synonymous_variant | 0.18 |
fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 0.17 |
fbiA | 3640416 | c.-127G>T | upstream_gene_variant | 0.14 |
fbiA | 3640541 | c.-2A>G | upstream_gene_variant | 0.14 |
fbiB | 3640560 | c.-975G>C | upstream_gene_variant | 0.17 |
fbiA | 3640562 | p.Ala7Val | missense_variant | 0.16 |
fbiB | 3640566 | c.-969T>G | upstream_gene_variant | 0.16 |
fbiB | 3640587 | c.-948C>T | upstream_gene_variant | 0.14 |
fbiB | 3640591 | c.-944_-942delCTCinsTTG | upstream_gene_variant | 0.14 |
fbiB | 3640606 | c.-929C>T | upstream_gene_variant | 0.14 |
alr | 3840248 | c.1173C>A | synonymous_variant | 0.17 |
alr | 3840272 | c.1149C>G | synonymous_variant | 0.23 |
alr | 3840275 | c.1146T>G | synonymous_variant | 0.24 |
alr | 3840332 | c.1089G>C | synonymous_variant | 0.17 |
alr | 3840416 | p.Cys335Arg | missense_variant | 0.17 |
alr | 3840422 | c.997_999delAGAinsCGG | synonymous_variant | 0.17 |
alr | 3840443 | c.978G>C | synonymous_variant | 0.17 |
alr | 3840446 | c.975G>T | synonymous_variant | 0.16 |
rpoA | 3877533 | c.975C>G | synonymous_variant | 0.18 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.15 |
rpoA | 3877567 | p.Ser314Thr | missense_variant | 0.19 |
rpoA | 3877569 | c.939G>C | synonymous_variant | 0.21 |
rpoA | 3877575 | c.933C>T | synonymous_variant | 0.19 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.21 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.17 |
rpoA | 3877620 | c.888G>A | synonymous_variant | 0.21 |
rpoA | 3877647 | c.861C>A | synonymous_variant | 0.24 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.23 |
rpoA | 3877659 | c.849G>A | synonymous_variant | 0.23 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.27 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.27 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.23 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.23 |
rpoA | 3877685 | c.823C>T | synonymous_variant | 0.24 |
rpoA | 3877689 | c.819C>T | synonymous_variant | 0.24 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.24 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.3 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.26 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.28 |
rpoA | 3877737 | c.771G>T | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.24 |
rpoA | 3877746 | c.762G>C | synonymous_variant | 0.25 |
rpoA | 3877752 | c.756C>T | synonymous_variant | 0.27 |
rpoA | 3877755 | c.753C>A | synonymous_variant | 0.27 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.21 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.25 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.24 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.24 |
rpoA | 3877830 | c.678C>T | synonymous_variant | 0.26 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.27 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.29 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.3 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.32 |
rpoA | 3877886 | c.622C>T | synonymous_variant | 0.25 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.22 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.22 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.19 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.19 |
rpoA | 3877929 | c.579C>T | synonymous_variant | 0.19 |
rpoA | 3877950 | c.558C>T | synonymous_variant | 0.22 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.27 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.25 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.28 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.26 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.29 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.32 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.32 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.3 |
rpoA | 3878043 | c.465G>T | synonymous_variant | 0.32 |
rpoA | 3878058 | c.450G>C | synonymous_variant | 0.31 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.32 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.33 |
rpoA | 3878085 | c.423G>A | synonymous_variant | 0.37 |
rpoA | 3878097 | c.411G>A | synonymous_variant | 0.33 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.33 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.35 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.29 |
rpoA | 3878126 | c.382C>T | synonymous_variant | 0.27 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.26 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.37 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.37 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.32 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.34 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.36 |
rpoA | 3878211 | c.297G>A | synonymous_variant | 0.38 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.38 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.37 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.35 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.33 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.34 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.31 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.29 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.31 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.28 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.2 |
rpoA | 3878442 | p.Val22Thr | missense_variant | 0.17 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 0.23 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.24 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.25 |
rpoA | 3878483 | c.25C>T | synonymous_variant | 0.26 |
rpoA | 3878490 | c.18C>T | synonymous_variant | 0.27 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.3 |
rpoA | 3878512 | c.-6_-5insGAA | upstream_gene_variant | 0.29 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.33 |
rpoA | 3878680 | c.-173C>T | upstream_gene_variant | 0.38 |
rpoA | 3878698 | c.-191A>C | upstream_gene_variant | 0.4 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.22 |
ddn | 3986657 | c.-187C>G | upstream_gene_variant | 0.22 |
ddn | 3986663 | c.-181G>A | upstream_gene_variant | 0.21 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.21 |
ddn | 3986696 | c.-148G>T | upstream_gene_variant | 0.17 |
ddn | 3986711 | c.-133C>G | upstream_gene_variant | 0.22 |
ddn | 3986930 | c.87C>T | synonymous_variant | 0.15 |
ddn | 3986933 | c.90C>A | synonymous_variant | 0.16 |
ddn | 3986941 | p.Asp33Gly | missense_variant | 0.17 |
ddn | 3986945 | c.102G>C | synonymous_variant | 0.16 |
ddn | 3986951 | c.108T>C | synonymous_variant | 0.16 |
ddn | 3986954 | c.111G>C | synonymous_variant | 0.16 |
ddn | 3986957 | c.114C>T | synonymous_variant | 0.15 |
ddn | 3986975 | c.132T>C | synonymous_variant | 0.15 |
ddn | 3986984 | c.141G>T | synonymous_variant | 0.18 |
ddn | 3987020 | c.177G>A | synonymous_variant | 0.19 |
ddn | 3987065 | c.222T>C | synonymous_variant | 0.15 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.15 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.2 |
clpC1 | 4038308 | c.2397G>C | synonymous_variant | 0.16 |
clpC1 | 4038314 | c.2391T>G | synonymous_variant | 0.15 |
clpC1 | 4038436 | p.Ala757Ser | missense_variant | 0.21 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.21 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.22 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.24 |
clpC1 | 4038508 | c.2197C>T | synonymous_variant | 0.31 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.34 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.32 |
clpC1 | 4038533 | c.2172C>T | synonymous_variant | 0.3 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.31 |
clpC1 | 4038602 | c.2103G>C | synonymous_variant | 0.14 |
clpC1 | 4038695 | c.2010C>A | synonymous_variant | 0.17 |
clpC1 | 4038698 | c.2007C>G | synonymous_variant | 0.17 |
clpC1 | 4038703 | c.2002C>T | synonymous_variant | 0.15 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.16 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.16 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.2 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.22 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.32 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.24 |
clpC1 | 4038800 | c.1905C>T | synonymous_variant | 0.24 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.23 |
clpC1 | 4038838 | c.1867C>T | synonymous_variant | 0.2 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.2 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.2 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.15 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.16 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.15 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.15 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.17 |
clpC1 | 4038995 | c.1710G>A | synonymous_variant | 0.21 |
clpC1 | 4039009 | c.1696C>T | synonymous_variant | 0.26 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.25 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.26 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.36 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.38 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.38 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.28 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.28 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.32 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.27 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.21 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.22 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.22 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.15 |
clpC1 | 4039295 | c.1410A>G | synonymous_variant | 0.16 |
clpC1 | 4039337 | c.1368A>C | synonymous_variant | 0.21 |
clpC1 | 4039352 | c.1353C>T | synonymous_variant | 0.21 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.19 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.19 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.19 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.16 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.16 |
clpC1 | 4039493 | c.1212C>T | synonymous_variant | 0.15 |
clpC1 | 4039514 | c.1191C>T | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.16 |
clpC1 | 4039693 | c.1012C>T | synonymous_variant | 0.27 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.27 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039733 | c.972G>A | synonymous_variant | 0.22 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.2 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.16 |
clpC1 | 4039942 | c.763C>T | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.17 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.18 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.24 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.22 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.2 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.23 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.21 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.29 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.31 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.31 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.31 |
clpC1 | 4040091 | c.613_614delTCinsAG | synonymous_variant | 0.31 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.31 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.29 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.19 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.18 |
clpC1 | 4040300 | c.405C>T | synonymous_variant | 0.17 |
clpC1 | 4040636 | c.69C>G | synonymous_variant | 0.2 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.17 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.17 |
clpC1 | 4040674 | c.31A>C | synonymous_variant | 0.16 |
embC | 4239693 | c.-170_-168delGCAinsACG | upstream_gene_variant | 0.17 |
embC | 4240123 | c.261C>G | synonymous_variant | 0.15 |
embC | 4240128 | p.Gln89Arg | missense_variant | 0.16 |
embC | 4240150 | c.288A>G | synonymous_variant | 0.18 |
embC | 4240151 | p.Ser97Pro | missense_variant | 0.18 |
embC | 4240171 | c.309G>C | synonymous_variant | 0.16 |
embC | 4240175 | c.313T>C | synonymous_variant | 0.15 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.19 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.17 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.17 |
embC | 4240795 | c.933C>G | synonymous_variant | 0.16 |
embC | 4240831 | c.969T>C | synonymous_variant | 0.2 |
embC | 4240858 | c.996G>A | synonymous_variant | 0.16 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.18 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.17 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.22 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.18 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.18 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.21 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.36 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.3 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.18 |
embC | 4241153 | p.Ile431Leu | missense_variant | 0.2 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.16 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.16 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.19 |
embC | 4241761 | c.1899G>C | synonymous_variant | 0.17 |
embC | 4241788 | c.1926C>T | synonymous_variant | 0.24 |
embC | 4241791 | c.1929G>C | synonymous_variant | 0.25 |
embC | 4241797 | c.1935C>T | synonymous_variant | 0.25 |
embC | 4241809 | c.1947A>G | synonymous_variant | 0.17 |
embC | 4241818 | c.1956C>T | synonymous_variant | 0.15 |
embC | 4241821 | c.1959G>A | synonymous_variant | 0.16 |
embC | 4242092 | p.Leu744Val | missense_variant | 0.14 |
embC | 4242106 | c.2244C>G | synonymous_variant | 0.15 |
embA | 4242505 | c.-728G>A | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.18 |
embA | 4242838 | c.-395C>G | upstream_gene_variant | 0.25 |
embA | 4242844 | c.-389A>G | upstream_gene_variant | 0.28 |
embA | 4242847 | c.-386C>A | upstream_gene_variant | 0.27 |
embA | 4242859 | c.-374C>T | upstream_gene_variant | 0.23 |
embC | 4242863 | p.Tyr1001Asn | missense_variant | 0.23 |
embA | 4242871 | c.-362C>T | upstream_gene_variant | 0.25 |
embC | 4242873 | p.Asp1004Val | missense_variant | 0.25 |
embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.28 |
embC | 4242885 | p.Lys1008Thr | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244120 | c.888T>C | synonymous_variant | 0.16 |
embA | 4244165 | c.933T>G | synonymous_variant | 0.14 |
embA | 4244170 | p.Gln313Arg | missense_variant | 0.16 |
embA | 4244178 | p.Ala316Ser | missense_variant | 0.2 |
embA | 4244198 | c.966C>A | synonymous_variant | 0.22 |
embA | 4244207 | c.975C>G | synonymous_variant | 0.18 |
embA | 4244213 | c.981C>G | synonymous_variant | 0.19 |
embA | 4244219 | c.987C>G | synonymous_variant | 0.17 |
embA | 4244228 | c.996A>G | synonymous_variant | 0.15 |
embA | 4244233 | p.Ala334Gly | missense_variant | 0.15 |
embA | 4244252 | c.1020C>T | synonymous_variant | 0.14 |
embA | 4244260 | p.Val343Ala | missense_variant | 0.15 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.18 |
embA | 4244345 | c.1113C>G | synonymous_variant | 0.18 |
embA | 4244856 | p.Ala542Pro | missense_variant | 0.23 |
embA | 4244885 | c.1653A>G | synonymous_variant | 0.22 |
embA | 4244897 | c.1665T>G | synonymous_variant | 0.15 |
embA | 4244921 | c.1689C>G | synonymous_variant | 0.15 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.23 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.21 |
embA | 4245110 | c.1878C>T | synonymous_variant | 0.18 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.18 |
embA | 4245224 | c.1992T>C | synonymous_variant | 0.15 |
embB | 4245620 | c.-894T>C | upstream_gene_variant | 0.15 |
embB | 4245623 | c.-891G>A | upstream_gene_variant | 0.16 |
embB | 4245662 | c.-852G>C | upstream_gene_variant | 0.32 |
embB | 4245674 | c.-840A>T | upstream_gene_variant | 0.32 |
embB | 4245677 | c.-837G>C | upstream_gene_variant | 0.31 |
embB | 4245683 | c.-831C>T | upstream_gene_variant | 0.32 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.38 |
embB | 4245714 | c.-800C>T | upstream_gene_variant | 0.43 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.4 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.4 |
embB | 4245734 | c.-780G>C | upstream_gene_variant | 0.33 |
embB | 4245737 | c.-777A>T | upstream_gene_variant | 0.31 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.24 |
embA | 4245772 | p.Asn847Thr | missense_variant | 0.25 |
embB | 4245803 | c.-711C>T | upstream_gene_variant | 0.25 |
embB | 4245806 | c.-708G>A | upstream_gene_variant | 0.24 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.21 |
embB | 4245812 | c.-702G>T | upstream_gene_variant | 0.2 |
embA | 4245813 | p.Pro861Ala | missense_variant | 0.2 |
embA | 4245822 | p.Pro864Ala | missense_variant | 0.19 |
embB | 4245839 | c.-675G>C | upstream_gene_variant | 0.18 |
embA | 4245843 | p.Val871Ile | missense_variant | 0.14 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.17 |
embB | 4245851 | c.-663G>C | upstream_gene_variant | 0.17 |
embB | 4245857 | c.-657C>G | upstream_gene_variant | 0.17 |
embB | 4245875 | c.-639G>A | upstream_gene_variant | 0.19 |
embA | 4245978 | p.Ile916Leu | missense_variant | 0.21 |
embB | 4245983 | c.-531A>G | upstream_gene_variant | 0.24 |
embB | 4245992 | c.-522C>G | upstream_gene_variant | 0.28 |
embB | 4246004 | c.-510T>C | upstream_gene_variant | 0.33 |
embB | 4246005 | c.-509C>T | upstream_gene_variant | 0.33 |
embB | 4246013 | c.-501T>C | upstream_gene_variant | 0.32 |
embA | 4246020 | p.Ala930Thr | missense_variant | 0.32 |
embB | 4246028 | c.-486G>C | upstream_gene_variant | 0.32 |
embB | 4246070 | c.-444G>C | upstream_gene_variant | 0.37 |
embB | 4246082 | c.-432T>C | upstream_gene_variant | 0.29 |
embB | 4246109 | c.-405C>G | upstream_gene_variant | 0.32 |
embB | 4246115 | c.-399T>C | upstream_gene_variant | 0.33 |
embA | 4246128 | p.Ser966Thr | missense_variant | 0.25 |
embA | 4246138 | p.Arg969Gln | missense_variant | 0.18 |
embB | 4246140 | c.-374T>C | upstream_gene_variant | 0.18 |
embB | 4246148 | c.-366G>C | upstream_gene_variant | 0.18 |
embB | 4246151 | c.-363A>C | upstream_gene_variant | 0.18 |
embA | 4246152 | p.Ala974Arg | missense_variant | 0.18 |
embB | 4246172 | c.-342C>T | upstream_gene_variant | 0.24 |
embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.36 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.24 |
embB | 4246211 | c.-303T>C | upstream_gene_variant | 0.21 |
embB | 4246217 | c.-297G>A | upstream_gene_variant | 0.22 |
embB | 4246220 | c.-294T>C | upstream_gene_variant | 0.23 |
embB | 4246223 | c.-291C>T | upstream_gene_variant | 0.23 |
embA | 4246227 | p.Ile999Val | missense_variant | 0.24 |
embB | 4246235 | c.-279G>A | upstream_gene_variant | 0.24 |
embB | 4246244 | c.-270G>A | upstream_gene_variant | 0.25 |
embA | 4246254 | p.Leu1008Met | missense_variant | 0.32 |
embB | 4246259 | c.-255G>C | upstream_gene_variant | 0.31 |
embB | 4246265 | c.-249C>T | upstream_gene_variant | 0.3 |
embB | 4246268 | c.-246G>A | upstream_gene_variant | 0.31 |
embA | 4246279 | p.Ala1016Val | missense_variant | 0.37 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.22 |
embB | 4246307 | c.-207G>C | upstream_gene_variant | 0.23 |
embB | 4246316 | c.-198T>C | upstream_gene_variant | 0.24 |
embB | 4246346 | c.-168C>G | upstream_gene_variant | 0.24 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.16 |
embB | 4246828 | c.315A>G | synonymous_variant | 0.16 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.16 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.21 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.21 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.21 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.28 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.27 |
embB | 4247555 | p.Leu348Ile | missense_variant | 0.28 |
embB | 4247566 | c.1053C>G | synonymous_variant | 0.26 |
embB | 4247579 | p.Ala356Phe | missense_variant | 0.26 |
embB | 4247590 | c.1077A>G | synonymous_variant | 0.25 |
embB | 4247608 | c.1095G>C | synonymous_variant | 0.23 |
embB | 4247611 | c.1098G>C | synonymous_variant | 0.21 |
embB | 4247632 | c.1119C>G | synonymous_variant | 0.2 |
embB | 4247722 | c.1209G>C | synonymous_variant | 0.16 |
embB | 4247725 | c.1212G>C | synonymous_variant | 0.16 |
embB | 4247779 | c.1266C>G | synonymous_variant | 0.14 |
embB | 4247785 | c.1272G>C | synonymous_variant | 0.18 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.18 |
embB | 4247911 | p.Leu466Phe | missense_variant | 0.17 |
embB | 4247915 | p.Arg468Asn | missense_variant | 0.17 |
embB | 4247920 | c.1407T>C | synonymous_variant | 0.15 |
embB | 4247923 | c.1410T>C | synonymous_variant | 0.17 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.23 |
embB | 4247948 | p.Val479Leu | missense_variant | 0.29 |
embB | 4247975 | p.Val488Ile | missense_variant | 0.21 |
embB | 4247989 | c.1476G>C | synonymous_variant | 0.2 |
embB | 4248001 | c.1488C>T | synonymous_variant | 0.18 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.17 |
embB | 4248042 | p.Ala510Gly | missense_variant | 0.19 |
embB | 4248052 | c.1539G>T | synonymous_variant | 0.19 |
embB | 4248055 | c.1542G>C | synonymous_variant | 0.19 |
embB | 4248058 | c.1545C>T | synonymous_variant | 0.19 |
embB | 4248061 | c.1548G>A | synonymous_variant | 0.18 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.18 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.22 |
embB | 4248094 | c.1581C>T | synonymous_variant | 0.3 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.32 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.24 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.24 |
embB | 4248154 | c.1641G>T | synonymous_variant | 0.23 |
embB | 4248157 | c.1644A>T | synonymous_variant | 0.21 |
embB | 4248163 | c.1650G>A | synonymous_variant | 0.22 |
embB | 4248169 | c.1656C>T | synonymous_variant | 0.22 |
embB | 4248175 | c.1662G>A | synonymous_variant | 0.24 |
embB | 4248178 | c.1665C>T | synonymous_variant | 0.23 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.28 |
embB | 4248214 | c.1701C>G | synonymous_variant | 0.27 |
embB | 4248217 | c.1704C>G | synonymous_variant | 0.27 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.27 |
embB | 4248233 | c.1720C>T | synonymous_variant | 0.28 |
embB | 4248252 | p.Gly580Ala | missense_variant | 0.29 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.29 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.23 |
embB | 4248280 | c.1767C>G | synonymous_variant | 0.24 |
embB | 4248424 | c.1911G>A | synonymous_variant | 0.19 |
embB | 4248430 | c.1917T>C | synonymous_variant | 0.19 |
embB | 4248448 | c.1935C>T | synonymous_variant | 0.16 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.19 |
embB | 4248472 | c.1959T>C | synonymous_variant | 0.18 |
embB | 4248496 | c.1983G>C | synonymous_variant | 0.23 |
embB | 4248504 | p.Asp664Ala | missense_variant | 0.22 |
embB | 4248508 | c.1995G>A | synonymous_variant | 0.19 |
embB | 4248514 | c.2001A>G | synonymous_variant | 0.19 |
embB | 4248682 | c.2169G>C | synonymous_variant | 0.17 |
embB | 4248697 | c.2184A>C | synonymous_variant | 0.15 |
embB | 4249568 | p.Ser1019Asn | missense_variant | 0.19 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.23 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.21 |
embB | 4249607 | p.Thr1032Val | missense_variant | 0.17 |
embB | 4249618 | c.3105C>G | synonymous_variant | 0.19 |
embB | 4249624 | c.3111C>T | synonymous_variant | 0.19 |
embB | 4249627 | c.3114G>C | synonymous_variant | 0.18 |
embB | 4249640 | c.3127T>C | synonymous_variant | 0.22 |
embB | 4249648 | c.3135G>C | synonymous_variant | 0.22 |
embB | 4249654 | c.3141C>T | synonymous_variant | 0.14 |
embB | 4249675 | c.3162C>G | synonymous_variant | 0.25 |
embB | 4249693 | c.3180T>C | synonymous_variant | 0.33 |
embB | 4249699 | c.3186T>A | synonymous_variant | 0.33 |
embB | 4249702 | c.3189C>A | synonymous_variant | 0.33 |
embB | 4249703 | c.3190C>T | synonymous_variant | 0.33 |
embB | 4249711 | c.3198G>A | synonymous_variant | 0.41 |
embB | 4249735 | c.3222T>G | synonymous_variant | 0.44 |
embB | 4249741 | c.3228C>A | synonymous_variant | 0.4 |
embB | 4249744 | c.3231G>A | synonymous_variant | 0.31 |
embB | 4249750 | p.Glu1079Asp | missense_variant | 0.29 |
embB | 4249751 | c.3238T>C | synonymous_variant | 0.29 |
aftB | 4267499 | c.1338G>C | synonymous_variant | 0.16 |
aftB | 4267510 | p.Asn443Asp | missense_variant | 0.15 |
aftB | 4267511 | c.1326C>T | synonymous_variant | 0.15 |
aftB | 4267529 | c.1308T>C | synonymous_variant | 0.26 |
aftB | 4267535 | c.1302A>G | synonymous_variant | 0.26 |
aftB | 4267556 | c.1281G>C | synonymous_variant | 0.28 |
aftB | 4267574 | c.1263G>C | synonymous_variant | 0.18 |
aftB | 4267580 | c.1257G>A | synonymous_variant | 0.28 |
aftB | 4267592 | c.1245C>G | synonymous_variant | 0.26 |
aftB | 4267622 | p.Ser405Thr | missense_variant | 0.24 |
aftB | 4267634 | p.Arg401His | missense_variant | 0.21 |
aftB | 4267637 | c.1200C>G | synonymous_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.73 |
aftB | 4267649 | c.1188T>C | synonymous_variant | 0.27 |
aftB | 4267667 | c.1170A>G | synonymous_variant | 0.22 |
aftB | 4267670 | c.1167G>A | synonymous_variant | 0.25 |
aftB | 4267781 | c.1056C>A | synonymous_variant | 0.22 |
aftB | 4267785 | p.Gly351Ala | missense_variant | 0.3 |
aftB | 4267793 | c.1044C>T | synonymous_variant | 0.3 |
aftB | 4267802 | c.1035T>C | synonymous_variant | 0.33 |
aftB | 4267805 | c.1032T>C | synonymous_variant | 0.33 |
aftB | 4267808 | c.1029G>C | synonymous_variant | 0.33 |
aftB | 4267826 | c.1011G>C | synonymous_variant | 0.36 |
aftB | 4267838 | c.999T>C | synonymous_variant | 0.57 |
aftB | 4267841 | c.996C>T | synonymous_variant | 0.57 |
aftB | 4267856 | c.981T>C | synonymous_variant | 0.71 |
aftB | 4267879 | p.Val320Leu | missense_variant | 0.5 |
aftB | 4267891 | p.Val316Ile | missense_variant | 0.33 |
aftB | 4267892 | p.Ile315Met | missense_variant | 0.33 |
aftB | 4267898 | c.939T>C | synonymous_variant | 0.33 |
aftB | 4267907 | c.930C>G | synonymous_variant | 0.22 |
aftB | 4267912 | p.Pro309Ala | missense_variant | 0.2 |
aftB | 4267916 | c.921T>C | synonymous_variant | 0.18 |
aftB | 4267919 | c.918A>G | synonymous_variant | 0.18 |
aftB | 4267922 | c.915G>A | synonymous_variant | 0.18 |
aftB | 4267940 | c.897T>G | synonymous_variant | 0.17 |
aftB | 4268194 | p.Leu215Val | missense_variant | 0.15 |
aftB | 4268207 | c.630C>G | synonymous_variant | 0.17 |
aftB | 4268213 | c.624T>C | synonymous_variant | 0.16 |
aftB | 4268228 | c.609C>G | synonymous_variant | 0.15 |
ubiA | 4268956 | p.Ala293Gly | missense_variant | 0.21 |
aftB | 4268978 | c.-142C>T | upstream_gene_variant | 0.34 |
aftB | 4268994 | c.-158T>C | upstream_gene_variant | 0.39 |
aftB | 4269000 | c.-164G>A | upstream_gene_variant | 0.39 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.41 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.39 |
aftB | 4269027 | c.-191C>G | upstream_gene_variant | 0.37 |
aftB | 4269030 | c.-194C>G | upstream_gene_variant | 0.39 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.37 |
aftB | 4269045 | c.-209G>C | upstream_gene_variant | 0.37 |
aftB | 4269177 | c.-341G>A | upstream_gene_variant | 0.17 |
aftB | 4269180 | c.-344G>T | upstream_gene_variant | 0.19 |
aftB | 4269195 | c.-359C>T | upstream_gene_variant | 0.2 |
aftB | 4269216 | c.-380C>T | upstream_gene_variant | 0.2 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.16 |
aftB | 4269225 | c.-389C>T | upstream_gene_variant | 0.16 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.15 |
ubiA | 4269688 | p.Val49Ala | missense_variant | 0.15 |
aftB | 4269690 | c.-854C>T | upstream_gene_variant | 0.15 |
aftB | 4269705 | c.-869T>C | upstream_gene_variant | 0.15 |
ubiA | 4269710 | p.Gly42Arg | missense_variant | 0.15 |
ubiA | 4269715 | p.Leu40Ala | missense_variant | 0.15 |
aftB | 4269723 | c.-887G>C | upstream_gene_variant | 0.17 |
aftB | 4269744 | c.-908G>C | upstream_gene_variant | 0.19 |
ethA | 4326322 | c.1152T>C | synonymous_variant | 0.17 |
ethA | 4326331 | c.1143C>G | synonymous_variant | 0.18 |
ethA | 4326346 | c.1128C>G | synonymous_variant | 0.2 |
ethA | 4326352 | c.1122T>G | synonymous_variant | 0.2 |
ethA | 4326535 | c.939G>C | synonymous_variant | 0.18 |
ethR | 4326556 | c.-993A>G | upstream_gene_variant | 0.24 |
ethA | 4326563 | p.Ala304Gly | missense_variant | 0.22 |
ethR | 4326565 | c.-984C>A | upstream_gene_variant | 0.24 |
ethR | 4326591 | c.-958A>G | upstream_gene_variant | 0.21 |
ethR | 4326598 | c.-951T>C | upstream_gene_variant | 0.22 |
ethR | 4326610 | c.-939G>C | upstream_gene_variant | 0.17 |
ethR | 4326613 | c.-936G>A | upstream_gene_variant | 0.15 |
ethR | 4326880 | c.-669G>A | upstream_gene_variant | 0.14 |
ethR | 4326895 | c.-654C>T | upstream_gene_variant | 0.15 |
ethR | 4326901 | c.-648C>A | upstream_gene_variant | 0.15 |
ethA | 4326949 | p.Ala175Gly | missense_variant | 0.16 |
ethA | 4326952 | p.Asp174Glu | missense_variant | 0.17 |
ethA | 4327680 | c.-207A>G | upstream_gene_variant | 0.16 |
ethA | 4327695 | c.-222A>G | upstream_gene_variant | 0.21 |
ethA | 4327707 | c.-234G>C | upstream_gene_variant | 0.25 |
ethA | 4327710 | c.-237G>T | upstream_gene_variant | 0.23 |
ethA | 4327713 | c.-240A>T | upstream_gene_variant | 0.23 |
ethA | 4327716 | c.-243G>T | upstream_gene_variant | 0.21 |
ethA | 4327720 | c.-247T>G | upstream_gene_variant | 0.22 |
ethA | 4327765 | c.-292G>A | upstream_gene_variant | 0.26 |
ethA | 4327770 | c.-297G>C | upstream_gene_variant | 0.25 |
whiB6 | 4338593 | c.-73delT | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |