Run ID: ERR4819068
Sample name:
Date: 01-04-2023 15:54:25
Number of reads: 674576
Percentage reads mapped: 78.41
Strain: lineage4.1;lineage1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.43 |
lineage4.1 | Euro-American | T;X;H | None | 0.43 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.24 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.22 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.17 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.15 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.17 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.23 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.31 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.15 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.23 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.29 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.31 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.21 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.2 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.13 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.16 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.18 |
gyrA | 7108 | c.-194G>A | upstream_gene_variant | 0.25 |
gyrA | 7114 | c.-188C>A | upstream_gene_variant | 0.33 |
gyrB | 7124 | p.Ser629Thr | missense_variant | 0.29 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.29 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.29 |
gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.33 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.33 |
gyrA | 7361 | c.60C>T | synonymous_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.14 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.14 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.12 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.13 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.13 |
gyrA | 8096 | c.795T>A | synonymous_variant | 0.13 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.13 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.2 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.21 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.22 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.19 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.19 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.25 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.21 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.14 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.13 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.12 |
gyrA | 8435 | c.1134C>G | synonymous_variant | 0.24 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.27 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.2 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.15 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.17 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.13 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.15 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.15 |
gyrA | 8987 | c.1686C>A | synonymous_variant | 0.13 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490782 | c.-1G>C | upstream_gene_variant | 0.12 |
fgd1 | 490797 | c.15G>A | synonymous_variant | 0.17 |
fgd1 | 490800 | c.18A>C | synonymous_variant | 0.18 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.18 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.18 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.2 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.14 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 0.16 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.16 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.13 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.22 |
fgd1 | 491173 | c.391C>A | synonymous_variant | 0.17 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.2 |
fgd1 | 491184 | c.402A>G | synonymous_variant | 0.2 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.2 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.22 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.25 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.25 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.25 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.25 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.62 |
mshA | 575376 | p.Ser10Leu | missense_variant | 0.29 |
mshA | 575756 | c.409C>T | synonymous_variant | 0.13 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.17 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.15 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.2 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.2 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.26 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.2 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.24 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.19 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.22 |
mshA | 575917 | p.Asp190Glu | missense_variant | 0.2 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.2 |
mshA | 575924 | p.Gly193Ser | missense_variant | 0.2 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.18 |
mshA | 576293 | p.Ala316Ser | missense_variant | 0.17 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.12 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.16 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.2 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.21 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.2 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.21 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.13 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.29 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.14 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.15 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.27 |
rpoB | 760433 | c.627C>T | synonymous_variant | 0.14 |
rpoB | 760454 | c.648C>G | synonymous_variant | 0.15 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.15 |
rpoB | 760469 | c.663C>T | synonymous_variant | 0.15 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.29 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.14 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.13 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.33 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.4 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.29 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.29 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.29 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.29 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.25 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.38 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.43 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.38 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.29 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.22 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.33 |
rpoB | 760869 | p.Val355Leu | missense_variant | 0.25 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 0.22 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.18 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.25 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.17 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.15 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.18 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.18 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.2 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.18 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.2 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.14 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.19 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.14 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.14 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.13 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.15 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.13 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.15 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.18 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.16 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.16 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.16 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.14 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.18 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.25 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.25 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.29 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.29 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.2 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.15 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.17 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.13 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.45 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.15 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.18 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.38 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.12 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.31 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.31 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.15 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.21 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.12 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.14 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.14 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.78 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.88 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.22 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.27 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.27 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.3 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.2 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.22 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.22 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.2 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.33 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.15 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.38 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.13 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.17 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.14 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.21 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.13 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.27 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.13 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.19 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.21 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.14 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.18 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.14 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.15 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.19 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.16 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.16 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.5 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.47 |
rpoC | 765292 | c.1923G>C | synonymous_variant | 0.15 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.14 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.17 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.14 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.14 |
rpoC | 765329 | p.Ser654Gly | missense_variant | 0.14 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.25 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.25 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.21 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.14 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.14 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.19 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.16 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.19 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.15 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.15 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.15 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 0.15 |
rpoC | 766288 | c.2919C>G | synonymous_variant | 0.13 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.15 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.15 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.16 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.12 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.17 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.17 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.17 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.17 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.25 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.15 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.14 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.13 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.21 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.22 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.33 |
rpoC | 766660 | c.3291G>C | synonymous_variant | 0.29 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.32 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.26 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.17 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.25 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.25 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.29 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.36 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.3 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.27 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.25 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.23 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.18 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.18 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.2 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.17 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.36 |
mmpL5 | 777085 | p.Asn466Asp | missense_variant | 0.16 |
mmpL5 | 777095 | c.1386T>C | synonymous_variant | 0.18 |
mmpL5 | 777101 | c.1380C>G | synonymous_variant | 0.2 |
mmpL5 | 777110 | c.1371T>G | synonymous_variant | 0.21 |
mmpL5 | 777115 | p.Met456Leu | missense_variant | 0.23 |
mmpL5 | 777116 | c.1365C>T | synonymous_variant | 0.23 |
mmpL5 | 777133 | p.Val450Ile | missense_variant | 0.27 |
mmpL5 | 777158 | c.1323C>G | synonymous_variant | 0.67 |
mmpL5 | 777164 | c.1317C>G | synonymous_variant | 0.5 |
mmpL5 | 777170 | c.1311T>C | synonymous_variant | 0.45 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.36 |
mmpL5 | 777191 | c.1290C>G | synonymous_variant | 0.25 |
mmpL5 | 777194 | c.1287A>G | synonymous_variant | 0.25 |
mmpL5 | 777206 | c.1275A>G | synonymous_variant | 0.21 |
mmpL5 | 777212 | p.Ala423Thr | missense_variant | 0.2 |
mmpL5 | 777215 | c.1266C>G | synonymous_variant | 0.2 |
mmpL5 | 777218 | c.1263G>A | synonymous_variant | 0.21 |
mmpL5 | 777251 | c.1230C>G | synonymous_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.54 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.14 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.18 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.19 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.15 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.18 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.14 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.18 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.18 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.18 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.22 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.25 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.25 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 0.26 |
fbiC | 1304739 | c.1809C>T | synonymous_variant | 0.13 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.19 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.24 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.26 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.26 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.26 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.21 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.25 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.27 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.5 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.5 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.4 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.29 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.17 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473660 | n.3G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673329 | c.-111A>G | upstream_gene_variant | 0.14 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.14 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.21 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.19 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.14 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.13 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.13 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.18 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.17 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.21 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.2 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.18 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.18 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.2 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.17 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.18 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.15 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.29 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.18 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.16 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.33 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.33 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.14 |
rpsA | 1834073 | p.Lys178Arg | missense_variant | 0.15 |
rpsA | 1834081 | c.540C>T | synonymous_variant | 0.15 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.13 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.13 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.13 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.19 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.21 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.29 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.24 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.19 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.13 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.31 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.22 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.17 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.18 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.17 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.22 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.24 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.21 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102014 | c.1029C>G | synonymous_variant | 0.17 |
ndh | 2102020 | c.1023A>G | synonymous_variant | 0.17 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.15 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.17 |
katG | 2153981 | p.Tyr711His | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.23 |
katG | 2155399 | p.Asn238Thr | missense_variant | 0.22 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.2 |
katG | 2155695 | c.417C>G | synonymous_variant | 0.2 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.17 |
PPE35 | 2167780 | p.Asn945Tyr | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.42 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.18 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.2 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.57 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.38 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290009 | c.-768A>C | upstream_gene_variant | 0.21 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.19 |
pncA | 2290024 | c.-783C>G | upstream_gene_variant | 0.23 |
pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 0.25 |
pncA | 2290033 | c.-792C>G | upstream_gene_variant | 0.25 |
pncA | 2290038 | c.-797G>A | upstream_gene_variant | 0.23 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.21 |
pncA | 2290069 | c.-830_-828delAGCinsGGA | upstream_gene_variant | 0.15 |
pncA | 2290072 | c.-831T>C | upstream_gene_variant | 0.15 |
pncA | 2290075 | c.-834C>G | upstream_gene_variant | 0.15 |
pncA | 2290084 | c.-843T>C | upstream_gene_variant | 0.15 |
pncA | 2290087 | c.-846T>C | upstream_gene_variant | 0.15 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.5 |
kasA | 2518468 | c.354A>C | synonymous_variant | 0.18 |
kasA | 2518474 | c.360G>A | synonymous_variant | 0.18 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.22 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.27 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.27 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.27 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.18 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.18 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.22 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.2 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.2 |
kasA | 2518693 | c.579C>G | synonymous_variant | 0.18 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.18 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.18 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.18 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.17 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.17 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.15 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.14 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.23 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.27 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.36 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.44 |
eis | 2714743 | p.Trp197Leu | missense_variant | 0.13 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.43 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.13 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.18 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.14 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.12 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.33 |
Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 0.27 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.3 |
Rv2752c | 3065028 | p.Val388Ile | missense_variant | 0.27 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.23 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.23 |
Rv2752c | 3065052 | c.1140G>A | synonymous_variant | 0.23 |
Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.23 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.21 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.2 |
Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 0.2 |
Rv2752c | 3065082 | c.1110G>C | synonymous_variant | 0.2 |
Rv2752c | 3065087 | c.1105A>C | synonymous_variant | 0.2 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.2 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.14 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.13 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.15 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.15 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.15 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.14 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.19 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.24 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.14 |
thyX | 3067691 | p.Ile85Met | missense_variant | 0.14 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.12 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.14 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.21 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.18 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.18 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.2 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.22 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.18 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.17 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.15 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.18 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.13 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.43 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.95 |
fprA | 3474306 | c.300G>C | synonymous_variant | 0.22 |
fprA | 3474312 | c.306C>T | synonymous_variant | 0.22 |
fprA | 3474321 | c.315C>G | synonymous_variant | 0.22 |
fprA | 3474324 | c.318G>C | synonymous_variant | 0.22 |
fprA | 3474333 | c.327T>C | synonymous_variant | 0.22 |
fprA | 3474337 | p.Met111Ala | missense_variant | 0.18 |
fprA | 3474340 | c.334T>C | synonymous_variant | 0.17 |
fprA | 3474354 | c.348T>C | synonymous_variant | 0.15 |
fprA | 3474360 | p.Asp118Glu | missense_variant | 0.14 |
fprA | 3474361 | c.355C>T | synonymous_variant | 0.14 |
fprA | 3474372 | c.366T>C | synonymous_variant | 0.13 |
fprA | 3474393 | c.387C>G | synonymous_variant | 0.15 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.56 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.62 |
fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 0.14 |
fbiA | 3640871 | p.Ala110Gly | missense_variant | 0.15 |
fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 0.15 |
fbiB | 3640899 | c.-636G>C | upstream_gene_variant | 0.15 |
fbiA | 3640900 | p.Gln120Asn | missense_variant | 0.15 |
rpoA | 3877482 | c.1026C>G | synonymous_variant | 0.14 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.19 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.18 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.17 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.14 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.13 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.14 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.15 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.15 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.16 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.26 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.22 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.14 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.14 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.13 |
clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.14 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.15 |
clpC1 | 4038499 | p.Ser736Arg | missense_variant | 0.14 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.21 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.14 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.22 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.22 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.2 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.18 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.17 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.14 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.13 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.17 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.17 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.22 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.22 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.25 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.25 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.27 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.23 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.13 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.13 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.21 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.21 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.16 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.16 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.14 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.12 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.25 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.3 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.3 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.22 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.27 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.25 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.15 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.14 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.12 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.15 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.17 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.17 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.2 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.18 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.18 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.21 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.27 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.23 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.21 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.25 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.57 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.14 |
embC | 4240204 | c.342T>C | synonymous_variant | 0.17 |
embC | 4240210 | c.348C>G | synonymous_variant | 0.17 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.15 |
embC | 4240229 | p.Leu123Ile | missense_variant | 0.17 |
embC | 4240232 | p.Gln124Val | missense_variant | 0.15 |
embC | 4240258 | c.396T>G | synonymous_variant | 0.15 |
embC | 4240270 | c.408T>C | synonymous_variant | 0.13 |
embC | 4240277 | p.Leu139Val | missense_variant | 0.13 |
embC | 4240630 | c.768C>A | synonymous_variant | 0.15 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.15 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.15 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.15 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.87 |
embC | 4240677 | p.Gly272Ala | missense_variant | 0.14 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.14 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.17 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.14 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.4 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.2 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.2 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.2 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.2 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.2 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.14 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.17 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.13 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.17 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.17 |
embC | 4241218 | c.1356G>C | synonymous_variant | 0.13 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.14 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.14 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.15 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.13 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.15 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.15 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.25 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.27 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.27 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.27 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.27 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.18 |
embC | 4241521 | c.1659T>C | synonymous_variant | 0.18 |
embC | 4241551 | c.1689A>G | synonymous_variant | 0.14 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.17 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.17 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.14 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.15 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.25 |
embC | 4241635 | c.1773G>C | synonymous_variant | 0.22 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.29 |
embC | 4241648 | c.1786T>C | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.35 |
embA | 4243848 | p.Val206Met | missense_variant | 0.44 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.14 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.13 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.15 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.22 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.24 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.21 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.21 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.2 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.19 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.2 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.2 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.82 |
embB | 4247356 | c.843C>T | synonymous_variant | 0.57 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.6 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.13 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.14 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.14 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.17 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.2 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.17 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.17 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.17 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.17 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.2 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.2 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.2 |
aftB | 4268102 | c.735C>G | synonymous_variant | 0.12 |
aftB | 4268125 | p.Ser238Gly | missense_variant | 0.14 |
aftB | 4268129 | c.708T>G | synonymous_variant | 0.14 |
aftB | 4268138 | c.699A>C | synonymous_variant | 0.18 |
aftB | 4268169 | p.Ala223Gly | missense_variant | 0.15 |
aftB | 4268171 | c.666G>C | synonymous_variant | 0.15 |
aftB | 4268179 | c.658T>C | synonymous_variant | 0.14 |
aftB | 4268182 | p.Phe219Leu | missense_variant | 0.14 |
aftB | 4268183 | c.654A>T | synonymous_variant | 0.14 |
aftB | 4268193 | p.Leu215Ala | missense_variant | 0.14 |
aftB | 4268683 | p.Gly52Ser | missense_variant | 0.5 |
aftB | 4268994 | c.-158T>G | upstream_gene_variant | 0.14 |
aftB | 4268999 | c.-163C>T | upstream_gene_variant | 0.14 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.18 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.2 |
aftB | 4269027 | c.-191C>T | upstream_gene_variant | 0.18 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.17 |
aftB | 4269036 | c.-200C>G | upstream_gene_variant | 0.17 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.15 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.14 |
aftB | 4269081 | c.-245G>C | upstream_gene_variant | 0.14 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.47 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.56 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 0.62 |
whiB6 | 4338449 | p.Ala25Pro | missense_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.68 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.68 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.38 |