Run ID: SRR25827687
Sample name:
Date: 02-02-2024 14:37:04
Number of reads: 1904060
Percentage reads mapped: 39.52
Strain: lineage1.1.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00) |
Isoniazid | R | fabG1 c.-15C>T (1.00), inhA p.Ile21Thr (1.00) |
Ethambutol | R | embB p.Tyr334His (0.69), embB p.Leu359Ile (0.21) |
Pyrazinamide | ||
Streptomycin | R | rpsL p.Lys88Arg (0.69), rrs n.462C>T (0.40) |
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | fabG1 c.-15C>T (1.00), inhA p.Ile21Thr (1.00) |
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1.2.BCG | M.bovis | BCG | None | 0.12 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.99 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.69 | streptomycin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.4 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674263 | p.Ile21Thr | missense_variant | 1.0 | isoniazid, ethionamide |
embB | 4247513 | p.Tyr334His | missense_variant | 0.69 | ethambutol |
embB | 4247588 | p.Leu359Ile | missense_variant | 0.21 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.91 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.91 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 0.17 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.15 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 0.15 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.15 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.16 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.19 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.21 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.24 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.23 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.26 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.27 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.27 |
gyrA | 8234 | c.933T>C | synonymous_variant | 0.29 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.29 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.23 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.19 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.19 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.2 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.2 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.18 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.18 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.17 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.26 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.18 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.24 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.23 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.23 |
fgd1 | 491643 | c.861G>A | synonymous_variant | 0.23 |
fgd1 | 491646 | c.864G>C | synonymous_variant | 0.23 |
fgd1 | 491649 | c.867C>T | synonymous_variant | 0.24 |
fgd1 | 491658 | c.876A>G | synonymous_variant | 0.24 |
fgd1 | 491661 | c.879C>G | synonymous_variant | 0.23 |
fgd1 | 491673 | c.891A>C | synonymous_variant | 0.23 |
fgd1 | 491676 | c.894T>C | synonymous_variant | 0.21 |
fgd1 | 491679 | c.897A>G | synonymous_variant | 0.21 |
fgd1 | 491687 | p.Thr302Lys | missense_variant | 0.21 |
fgd1 | 491697 | c.915G>C | synonymous_variant | 0.2 |
fgd1 | 491709 | c.927A>G | synonymous_variant | 0.18 |
fgd1 | 491712 | c.930T>C | synonymous_variant | 0.16 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.18 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.18 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.18 |
ccsA | 620376 | c.486G>C | synonymous_variant | 0.19 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.18 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.19 |
ccsA | 620389 | c.499C>T | synonymous_variant | 0.19 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.19 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.19 |
ccsA | 620421 | c.531G>C | synonymous_variant | 0.2 |
ccsA | 620424 | c.534G>C | synonymous_variant | 0.21 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.2 |
ccsA | 620436 | c.546T>A | synonymous_variant | 0.19 |
ccsA | 620439 | c.549T>C | synonymous_variant | 0.2 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.2 |
ccsA | 620631 | c.741T>G | synonymous_variant | 0.19 |
ccsA | 620646 | c.756G>A | synonymous_variant | 0.26 |
ccsA | 620649 | c.759A>G | synonymous_variant | 0.27 |
ccsA | 620659 | c.769_771delCGCinsAGG | synonymous_variant | 0.3 |
ccsA | 620664 | c.774C>T | synonymous_variant | 0.3 |
ccsA | 620682 | c.792G>A | synonymous_variant | 0.31 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.32 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.33 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.32 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.32 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.29 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.29 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.3 |
ccsA | 620742 | c.852G>C | synonymous_variant | 0.29 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.28 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.28 |
ccsA | 620763 | c.873G>A | synonymous_variant | 0.27 |
ccsA | 620769 | c.879C>G | synonymous_variant | 0.28 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.22 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.21 |
ccsA | 620790 | c.900C>T | synonymous_variant | 0.16 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.31 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.34 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.39 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.38 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.45 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.46 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.48 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.53 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.52 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.48 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.48 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.43 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.4 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.39 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.36 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.21 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.18 |
rpoB | 760490 | c.684C>T | synonymous_variant | 0.85 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.22 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.22 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.23 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.23 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.28 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.31 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.31 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.32 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.33 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.31 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.31 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.31 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.28 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.28 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.17 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.25 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.26 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.26 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.35 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.35 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.36 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.43 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.43 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.41 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.41 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.39 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.36 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.36 |
rpoB | 761373 | p.Val523His | missense_variant | 0.36 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.36 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.35 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.33 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.29 |
rpoB | 761438 | c.1632G>C | synonymous_variant | 0.28 |
rpoB | 761439 | p.Asp545Lys | missense_variant | 0.28 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.29 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.3 |
rpoB | 761452 | p.Val549Glu | missense_variant | 0.29 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.28 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.31 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.29 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.3 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.29 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.3 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.3 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.32 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.3 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.3 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.3 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.29 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.25 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.23 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.19 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.2 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.21 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.16 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.16 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.23 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.33 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.37 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.36 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.35 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.34 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.34 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.32 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.35 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.39 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.39 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.38 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.35 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.33 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.33 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.33 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.33 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.35 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.36 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.37 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.37 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.39 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.38 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.36 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.32 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.32 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.26 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.26 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.27 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.3 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.26 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.27 |
rpoC | 762551 | c.-819C>G | upstream_gene_variant | 0.28 |
rpoC | 762581 | c.-789T>C | upstream_gene_variant | 0.16 |
rpoC | 762758 | c.-612G>C | upstream_gene_variant | 0.17 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.25 |
rpoB | 762785 | p.Asp993Glu | missense_variant | 0.26 |
rpoC | 762788 | c.-582G>C | upstream_gene_variant | 0.26 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.26 |
rpoC | 762794 | c.-576C>G | upstream_gene_variant | 0.28 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.29 |
rpoB | 762810 | p.Ala1002Ser | missense_variant | 0.3 |
rpoB | 762813 | p.Met1003Val | missense_variant | 0.3 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.3 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.31 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.32 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.3 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.29 |
rpoC | 762926 | c.-444C>T | upstream_gene_variant | 0.19 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.38 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.39 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.38 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.37 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.37 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.62 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.38 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.38 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.39 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.34 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.31 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.32 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.31 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.3 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.33 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.33 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.32 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.33 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.32 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.33 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.33 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.31 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.32 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.32 |
rpoC | 763253 | c.-117G>C | upstream_gene_variant | 0.29 |
rpoC | 763256 | c.-114G>A | upstream_gene_variant | 0.28 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.23 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.25 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.3 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.3 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.31 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.31 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.31 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.33 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.26 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.28 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.29 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.32 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.35 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.35 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.35 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.34 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.35 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.39 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.36 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.35 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.33 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.3 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.24 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.2 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.17 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.17 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.17 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.82 |
rpoC | 763886 | p.Arg173Ser | missense_variant | 0.82 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.21 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.21 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.22 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.23 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.27 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.31 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.32 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.3 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.31 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.32 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.34 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.36 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.39 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.43 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.41 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.4 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.41 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.44 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.45 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.44 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.43 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.41 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.39 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.39 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.38 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.21 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.23 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.35 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.42 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.5 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.43 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.45 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.45 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.48 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.48 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.49 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.52 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.44 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.43 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.31 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.32 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.35 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.35 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.41 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.4 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.39 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.39 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.37 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.37 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.36 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.36 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.36 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.36 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.35 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.29 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.3 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.3 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.29 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.28 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.26 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765292 | c.1923G>C | synonymous_variant | 0.16 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.18 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.19 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.24 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.24 |
rpoC | 765329 | p.Ser654Gly | missense_variant | 0.24 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.28 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.27 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.28 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.35 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.43 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.44 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.43 |
rpoC | 765463 | p.Asn698Lys | missense_variant | 0.62 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.43 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.44 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.47 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.46 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.41 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.41 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.4 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.42 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.43 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.4 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.4 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.38 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.4 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.4 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.4 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.4 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.42 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.41 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.39 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.4 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.39 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.38 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.39 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.39 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.41 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.43 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.41 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.42 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.42 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.37 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.29 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.25 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.24 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.18 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.17 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.21 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.24 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.26 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.34 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.32 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.34 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.36 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.36 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.31 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.31 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.29 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.21 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.16 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.17 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.23 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.32 |
rpoC | 766660 | c.3291G>C | synonymous_variant | 0.32 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.3 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.31 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.48 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.47 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.41 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.41 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.32 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.31 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.2 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.22 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.33 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.41 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.42 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.4 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.42 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.4 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.4 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.3 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.26 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.22 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.21 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
mmpL5 | 777158 | c.1323C>G | synonymous_variant | 0.16 |
mmpL5 | 777164 | c.1317C>G | synonymous_variant | 0.16 |
mmpL5 | 777170 | c.1311T>C | synonymous_variant | 0.17 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.17 |
mmpL5 | 777191 | c.1290C>G | synonymous_variant | 0.16 |
mmpL5 | 777206 | c.1275A>G | synonymous_variant | 0.16 |
mmpL5 | 777212 | p.Ala423Thr | missense_variant | 0.16 |
mmpL5 | 777215 | c.1266C>G | synonymous_variant | 0.17 |
mmpL5 | 777218 | c.1263G>A | synonymous_variant | 0.16 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781571 | c.12C>T | synonymous_variant | 0.19 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.23 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.23 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.23 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.28 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.32 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.38 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.39 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.49 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.46 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.46 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.46 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.47 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.47 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.48 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.48 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.48 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.46 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.37 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.37 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.3 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.26 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.27 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.28 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.25 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.26 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.28 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.25 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.27 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.29 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.29 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.51 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.51 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.51 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.51 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.53 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.52 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.51 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.49 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.49 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.49 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.39 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.37 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.39 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.38 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.38 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.34 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.34 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.35 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.31 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.31 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.29 |
rplC | 800875 | p.Val23Ile | missense_variant | 0.29 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.3 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.29 |
rplC | 800892 | c.84G>C | synonymous_variant | 0.29 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.29 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.25 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.16 |
rplC | 800939 | p.Arg44His | missense_variant | 0.15 |
rplC | 801195 | c.387G>C | synonymous_variant | 0.2 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.19 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.24 |
rplC | 801249 | c.441T>C | synonymous_variant | 0.24 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.25 |
rplC | 801264 | c.456C>T | synonymous_variant | 0.21 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.2 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.21 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.2 |
rplC | 801279 | c.471G>C | synonymous_variant | 0.2 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.2 |
rplC | 801285 | c.477G>C | synonymous_variant | 0.22 |
rplC | 801300 | c.492C>G | synonymous_variant | 0.26 |
rplC | 801309 | c.501C>G | synonymous_variant | 0.28 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.27 |
rplC | 801321 | c.513C>T | synonymous_variant | 0.24 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.24 |
rplC | 801339 | c.531T>C | synonymous_variant | 0.23 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.22 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.22 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.23 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.21 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.31 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.3 |
rplC | 801423 | c.615G>C | synonymous_variant | 0.28 |
rplC | 801426 | c.618C>G | synonymous_variant | 0.29 |
rplC | 801427 | p.Met207Val | missense_variant | 0.32 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.26 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.29 |
fbiC | 1303501 | c.571C>T | synonymous_variant | 0.16 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.19 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.19 |
fbiC | 1303521 | c.591C>T | synonymous_variant | 0.18 |
fbiC | 1303530 | c.600G>A | synonymous_variant | 0.18 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.17 |
fbiC | 1303539 | c.609G>C | synonymous_variant | 0.18 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.21 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.26 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.27 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.29 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.29 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.29 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.29 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.29 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.26 |
fbiC | 1303641 | c.711C>T | synonymous_variant | 0.26 |
fbiC | 1303650 | c.720G>C | synonymous_variant | 0.21 |
fbiC | 1303654 | c.724C>T | synonymous_variant | 0.16 |
fbiC | 1303659 | c.729T>C | synonymous_variant | 0.16 |
fbiC | 1303661 | p.Val244Ala | missense_variant | 0.16 |
fbiC | 1303663 | c.733C>T | synonymous_variant | 0.17 |
fbiC | 1303671 | c.741C>T | synonymous_variant | 0.22 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.23 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.23 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.25 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.24 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 0.22 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.24 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.2 |
fbiC | 1303731 | c.801A>C | synonymous_variant | 0.21 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 0.21 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.23 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.21 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.2 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.21 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.23 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 0.25 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.33 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.32 |
fbiC | 1303797 | c.867A>G | synonymous_variant | 0.37 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.35 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.34 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.32 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.33 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.33 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.32 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.38 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.37 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.36 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.34 |
fbiC | 1303944 | c.1014G>C | synonymous_variant | 0.26 |
fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.26 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.26 |
fbiC | 1303953 | p.Asp341Glu | missense_variant | 0.26 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.25 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.25 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.26 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.22 |
fbiC | 1303998 | c.1068T>G | synonymous_variant | 0.22 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.18 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.16 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.19 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.22 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.21 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.21 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.2 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.22 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.2 |
fbiC | 1304670 | c.1740G>C | synonymous_variant | 0.18 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 0.18 |
fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.18 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.19 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.2 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.16 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.16 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.16 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.22 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.23 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.24 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.24 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.23 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.22 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.24 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.2 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.2 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.2 |
fbiC | 1305012 | c.2082G>C | synonymous_variant | 0.17 |
fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.16 |
fbiC | 1305276 | c.2346G>C | synonymous_variant | 0.17 |
fbiC | 1305279 | p.His783Gln | missense_variant | 0.17 |
fbiC | 1305282 | c.2352T>C | synonymous_variant | 0.18 |
fbiC | 1305310 | p.Arg794Gly | missense_variant | 0.17 |
fbiC | 1305318 | c.2388C>G | synonymous_variant | 0.17 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.19 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.19 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 0.15 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.19 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.2 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.22 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.22 |
atpE | 1461158 | c.114T>G | synonymous_variant | 0.22 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.22 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.22 |
atpE | 1461185 | c.141G>T | synonymous_variant | 0.22 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.2 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.19 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472045 | n.200T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473123 | n.1278delAinsTT | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475761 | n.2104_2106delCGCinsGT | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.34 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.18 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 0.19 |
inhA | 1673985 | c.-217C>G | upstream_gene_variant | 0.25 |
fabG1 | 1674006 | p.Asp189Glu | missense_variant | 0.26 |
inhA | 1674015 | c.-187C>T | upstream_gene_variant | 0.23 |
inhA | 1674018 | c.-184G>C | upstream_gene_variant | 0.23 |
inhA | 1674021 | c.-181G>C | upstream_gene_variant | 0.23 |
inhA | 1674024 | c.-178T>C | upstream_gene_variant | 0.23 |
inhA | 1674033 | c.-169T>C | upstream_gene_variant | 0.23 |
fabG1 | 1674037 | p.Gln200Ala | missense_variant | 0.23 |
inhA | 1674042 | c.-160G>T | upstream_gene_variant | 0.24 |
fabG1 | 1674049 | p.Gln204Asp | missense_variant | 0.23 |
inhA | 1674054 | c.-148T>C | upstream_gene_variant | 0.23 |
inhA | 1674060 | c.-142A>G | upstream_gene_variant | 0.23 |
inhA | 1674063 | c.-139G>C | upstream_gene_variant | 0.23 |
fabG1 | 1674079 | p.Pro214Ala | missense_variant | 0.22 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.19 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.27 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.3 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.33 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.41 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.42 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.46 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.46 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.44 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.43 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.42 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.43 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.41 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.41 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.46 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.43 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.31 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.3 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.29 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.25 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.22 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.31 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.33 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.35 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.32 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.32 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.37 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.4 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.37 |
rpsA | 1834081 | c.540C>T | synonymous_variant | 0.23 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.23 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.28 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.29 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.3 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.36 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.32 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.33 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.34 |
rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 0.34 |
rpsA | 1834288 | c.747C>T | synonymous_variant | 0.66 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.35 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.34 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.18 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.26 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.26 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.26 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.26 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.28 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.29 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.28 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.28 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.27 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.26 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101804 | c.1239T>G | synonymous_variant | 0.19 |
ndh | 2101808 | p.Thr412Ser | missense_variant | 0.21 |
ndh | 2101830 | p.Ile405Val | missense_variant | 0.24 |
ndh | 2101837 | p.Ala402Val | missense_variant | 0.25 |
ndh | 2101885 | c.1158G>A | synonymous_variant | 0.2 |
ndh | 2101888 | c.1155T>C | synonymous_variant | 0.23 |
ndh | 2101894 | c.1149T>G | synonymous_variant | 0.25 |
ndh | 2101912 | c.1131G>C | synonymous_variant | 0.29 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.29 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.28 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.23 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.16 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.17 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.17 |
katG | 2155661 | p.Val151Ile | missense_variant | 0.21 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.2 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.21 |
katG | 2155695 | c.417C>G | synonymous_variant | 0.21 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.22 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.21 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.2 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.21 |
katG | 2155740 | p.Gly124Gln | missense_variant | 0.21 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.28 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.17 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.16 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.18 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.22 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.31 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.32 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.33 |
kasA | 2518693 | c.579C>G | synonymous_variant | 0.33 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.34 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.33 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.34 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.33 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.34 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.36 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.36 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.38 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.42 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.41 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.38 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.36 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.36 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.36 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.28 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.25 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.19 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.17 |
kasA | 2519196 | p.Thr361Ser | missense_variant | 0.25 |
kasA | 2519215 | c.1101C>T | synonymous_variant | 0.22 |
kasA | 2519218 | c.1104G>A | synonymous_variant | 0.23 |
kasA | 2519221 | c.1107G>C | synonymous_variant | 0.22 |
kasA | 2519227 | c.1113G>C | synonymous_variant | 0.2 |
kasA | 2519230 | c.1116C>T | synonymous_variant | 0.2 |
kasA | 2519236 | c.1122G>A | synonymous_variant | 0.2 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.2 |
kasA | 2519245 | c.1131T>C | synonymous_variant | 0.19 |
kasA | 2519260 | c.1146T>G | synonymous_variant | 0.19 |
kasA | 2519263 | c.1149C>T | synonymous_variant | 0.19 |
kasA | 2519266 | c.1152C>T | synonymous_variant | 0.19 |
kasA | 2519269 | c.1155C>T | synonymous_variant | 0.19 |
kasA | 2519272 | c.1158C>G | synonymous_variant | 0.18 |
kasA | 2519281 | c.1167G>T | synonymous_variant | 0.16 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746420 | c.1179A>C | synonymous_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyX | 3067223 | c.723G>C | synonymous_variant | 0.16 |
thyX | 3067232 | c.714C>G | synonymous_variant | 0.16 |
thyX | 3067249 | p.Thr233Ser | missense_variant | 0.16 |
thyX | 3067252 | p.Val232Met | missense_variant | 0.16 |
thyX | 3067284 | p.Ala221Gly | missense_variant | 0.16 |
thyX | 3067292 | c.654G>A | synonymous_variant | 0.16 |
thyX | 3067295 | c.651C>T | synonymous_variant | 0.15 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.16 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.18 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.19 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.23 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.24 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.31 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.31 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.32 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.32 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.33 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.32 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.29 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.26 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.27 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.27 |
thyX | 3067762 | c.184C>A | synonymous_variant | 0.16 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.17 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.19 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.16 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.18 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.2 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.21 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.2 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.2 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.2 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.2 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.19 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.16 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.16 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.17 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.19 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.19 |
thyA | 3073917 | c.555C>G | synonymous_variant | 0.19 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.19 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.2 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.2 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.19 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.19 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.19 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.16 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.16 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.19 |
thyA | 3074100 | p.Asp124Asn | missense_variant | 0.2 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.21 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.21 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.19 |
thyA | 3074154 | c.318T>C | synonymous_variant | 0.21 |
thyA | 3074157 | c.315C>G | synonymous_variant | 0.19 |
thyA | 3074160 | c.312A>G | synonymous_variant | 0.19 |
thyA | 3074163 | p.Ala103Thr | missense_variant | 0.2 |
thyA | 3074172 | c.300G>C | synonymous_variant | 0.19 |
thyA | 3074175 | c.297A>G | synonymous_variant | 0.19 |
thyA | 3074181 | c.291A>G | synonymous_variant | 0.19 |
thyA | 3074187 | c.285T>C | synonymous_variant | 0.19 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.2 |
thyA | 3074214 | c.258T>C | synonymous_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087672 | p.His285Asp | missense_variant | 0.22 |
ald | 3087680 | c.861G>C | synonymous_variant | 0.21 |
ald | 3087704 | c.885T>C | synonymous_variant | 0.22 |
ald | 3087716 | c.897G>C | synonymous_variant | 0.18 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.29 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.28 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.25 |
fprA | 3473848 | c.-159_-157delCAAinsGAG | upstream_gene_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.2 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.19 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.2 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.23 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.38 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.45 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.45 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.48 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.52 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.53 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.51 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.48 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.45 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.46 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.39 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.39 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.38 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.39 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.36 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.37 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.4 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.43 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.48 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.49 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.49 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.5 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.5 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.48 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.47 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.47 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.45 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.46 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.45 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.44 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.45 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.4 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.34 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.32 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.31 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.27 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.23 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.24 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.22 |
rpoA | 3878043 | c.465G>A | synonymous_variant | 0.22 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.21 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.19 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.19 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.19 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.19 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.19 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.22 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.21 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.24 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.29 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.35 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.38 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.38 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.38 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.4 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.4 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.43 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.42 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.42 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.42 |
rpoA | 3878340 | c.168C>T | synonymous_variant | 0.44 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.49 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.43 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.43 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.45 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.43 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.42 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.42 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.39 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.33 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.31 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.32 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.3 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.24 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.22 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.23 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.22 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.32 |
rpoA | 3878683 | c.-176G>C | upstream_gene_variant | 0.29 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.15 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.15 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.16 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.21 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.28 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.29 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.24 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.26 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.26 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.26 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.25 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.27 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.27 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.34 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.35 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.38 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.37 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.41 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.48 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.48 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.48 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.49 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.49 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.49 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.48 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.45 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.37 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.34 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.35 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.32 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.35 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.36 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.34 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.33 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.33 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.3 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.27 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.27 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.27 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.24 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.25 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.18 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.17 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.26 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.27 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.28 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.27 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.24 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.22 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.22 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.22 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.21 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.23 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.22 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.21 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.34 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.33 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.35 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.36 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.36 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.4 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.4 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.43 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.49 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.48 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.46 |
clpC1 | 4039625 | c.1080G>A | synonymous_variant | 0.43 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.37 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.32 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.22 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.21 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.22 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.21 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.22 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.22 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.24 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.23 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.25 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.27 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.26 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.26 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.25 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.25 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.25 |
clpC1 | 4040444 | c.261C>T | synonymous_variant | 0.17 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.16 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.17 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.17 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.17 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.17 |
clpC1 | 4040501 | c.204C>T | synonymous_variant | 0.24 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.75 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.24 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.22 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.21 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.21 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.21 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.2 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.19 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.18 |
clpC1 | 4040567 | c.138C>G | synonymous_variant | 0.17 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.17 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.17 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.17 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.17 |
clpC1 | 4040596 | c.109C>T | synonymous_variant | 0.18 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.18 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.17 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.17 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.17 |
embC | 4240178 | c.316T>C | synonymous_variant | 0.25 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.24 |
embC | 4240204 | c.342T>C | synonymous_variant | 0.24 |
embC | 4240210 | c.348C>G | synonymous_variant | 0.24 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.2 |
embC | 4240222 | c.360G>C | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.23 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.28 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.28 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.31 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.29 |
embC | 4240828 | c.966G>C | synonymous_variant | 0.27 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.27 |
embC | 4240867 | c.1005T>C | synonymous_variant | 0.22 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.17 |
embC | 4240873 | c.1011C>G | synonymous_variant | 0.17 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.17 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.16 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.83 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.17 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.17 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.18 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.28 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.29 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.29 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.31 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.29 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.24 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.24 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.24 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.24 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.24 |
embC | 4241351 | p.Ile497Val | missense_variant | 0.16 |
embC | 4241361 | p.Asn500Thr | missense_variant | 0.16 |
embC | 4241363 | p.Leu501Met | missense_variant | 0.16 |
embC | 4241374 | c.1512T>C | synonymous_variant | 0.2 |
embC | 4241380 | c.1518A>C | synonymous_variant | 0.2 |
embC | 4241383 | c.1521G>C | synonymous_variant | 0.2 |
embC | 4241392 | c.1530G>C | synonymous_variant | 0.23 |
embC | 4241394 | p.Lys511Ser | missense_variant | 0.22 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.22 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.19 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.18 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.18 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.17 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.17 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.16 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.16 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242715 | c.-518T>C | upstream_gene_variant | 0.15 |
embA | 4242742 | c.-491C>G | upstream_gene_variant | 0.25 |
embA | 4242748 | c.-485A>G | upstream_gene_variant | 0.27 |
embA | 4242754 | c.-479G>C | upstream_gene_variant | 0.29 |
embC | 4242764 | p.Val968Leu | missense_variant | 0.29 |
embC | 4242779 | p.Asn973Asp | missense_variant | 0.34 |
embC | 4242791 | p.Ala977Ser | missense_variant | 0.34 |
embA | 4242796 | c.-437G>C | upstream_gene_variant | 0.33 |
embA | 4242799 | c.-434T>C | upstream_gene_variant | 0.34 |
embA | 4242820 | c.-413G>C | upstream_gene_variant | 0.35 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.36 |
embA | 4242832 | c.-401A>C | upstream_gene_variant | 0.33 |
embA | 4242838 | c.-395C>G | upstream_gene_variant | 0.35 |
embA | 4242841 | c.-392C>T | upstream_gene_variant | 0.32 |
embA | 4242844 | c.-389A>G | upstream_gene_variant | 0.33 |
embA | 4242847 | c.-386C>A | upstream_gene_variant | 0.33 |
embA | 4242859 | c.-374C>T | upstream_gene_variant | 0.31 |
embA | 4242862 | c.-371A>G | upstream_gene_variant | 0.32 |
embC | 4242863 | p.Tyr1001Asn | missense_variant | 0.32 |
embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.29 |
embA | 4242892 | c.-341G>C | upstream_gene_variant | 0.24 |
embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.23 |
embA | 4242919 | c.-314A>G | upstream_gene_variant | 0.18 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245218 | c.1986C>T | synonymous_variant | 0.87 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246080 | p.Pro950Ser | missense_variant | 0.17 |
embB | 4246088 | c.-426A>G | upstream_gene_variant | 0.2 |
embB | 4246097 | c.-417C>G | upstream_gene_variant | 0.2 |
embB | 4246103 | c.-411C>G | upstream_gene_variant | 0.2 |
embB | 4246109 | c.-405C>G | upstream_gene_variant | 0.2 |
embB | 4246115 | c.-399T>G | upstream_gene_variant | 0.21 |
embA | 4246128 | p.Ser966Thr | missense_variant | 0.23 |
embA | 4246138 | p.Arg969Gln | missense_variant | 0.22 |
embB | 4246140 | c.-374T>C | upstream_gene_variant | 0.22 |
embA | 4246143 | p.Ile971Val | missense_variant | 0.22 |
embB | 4246151 | c.-363A>G | upstream_gene_variant | 0.23 |
embA | 4246152 | p.Ala974Gln | missense_variant | 0.22 |
embB | 4246157 | c.-357A>G | upstream_gene_variant | 0.22 |
embB | 4246164 | c.-350T>C | upstream_gene_variant | 0.22 |
embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.21 |
embB | 4246196 | c.-318C>G | upstream_gene_variant | 0.22 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.18 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.16 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.26 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.28 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.31 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.29 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.3 |
embB | 4247566 | c.1053C>A | synonymous_variant | 0.26 |
embB | 4247572 | c.1059A>G | synonymous_variant | 0.25 |
embB | 4247579 | p.Ala356Phe | missense_variant | 0.21 |
embB | 4247587 | c.1074G>A | synonymous_variant | 0.21 |
embB | 4247603 | c.1090C>T | synonymous_variant | 0.2 |
embB | 4247611 | c.1098G>T | synonymous_variant | 0.19 |
embB | 4247614 | c.1101T>C | synonymous_variant | 0.2 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.16 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.18 |
embB | 4247797 | c.1284C>G | synonymous_variant | 0.25 |
embB | 4247800 | c.1287A>T | synonymous_variant | 0.25 |
embB | 4247803 | c.1290G>C | synonymous_variant | 0.24 |
embB | 4247815 | c.1302C>G | synonymous_variant | 0.22 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.22 |
embB | 4247830 | c.1317A>G | synonymous_variant | 0.2 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.19 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.21 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.19 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.17 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.17 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.16 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.15 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.18 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.16 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.16 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.18 |
embB | 4248199 | c.1686A>G | synonymous_variant | 0.24 |
embB | 4248200 | p.Ile563Val | missense_variant | 0.24 |
embB | 4248205 | c.1692C>G | synonymous_variant | 0.24 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.24 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.24 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.17 |
embB | 4249375 | c.2862G>C | synonymous_variant | 0.2 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.19 |
embB | 4249384 | c.2871G>T | synonymous_variant | 0.2 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.22 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.19 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.19 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.21 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.23 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.25 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.25 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.36 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.4 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.41 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.34 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.33 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.34 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.33 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.33 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.33 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.33 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.3 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.28 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.28 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.25 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.21 |
aftB | 4267268 | c.1569T>C | synonymous_variant | 0.16 |
aftB | 4267325 | c.1512G>C | synonymous_variant | 0.16 |
aftB | 4267334 | c.1503T>C | synonymous_variant | 0.17 |
aftB | 4268123 | c.714T>C | synonymous_variant | 0.16 |
aftB | 4268129 | c.708T>G | synonymous_variant | 0.16 |
aftB | 4268138 | c.699A>C | synonymous_variant | 0.17 |
aftB | 4268164 | p.Gln225Glu | missense_variant | 0.18 |
aftB | 4268169 | p.Ala223Gly | missense_variant | 0.17 |
aftB | 4268171 | c.666G>C | synonymous_variant | 0.17 |
aftB | 4268182 | p.Phe219Leu | missense_variant | 0.17 |
aftB | 4268183 | c.654A>T | synonymous_variant | 0.17 |
aftB | 4268193 | p.Leu215Ala | missense_variant | 0.17 |
aftB | 4268205 | p.Val211Ala | missense_variant | 0.16 |
ubiA | 4269031 | p.Gly268Asp | missense_variant | 0.9 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |