Run ID: SRR21677886
Sample name:
Date: 04-04-2023 02:49:36
Number of reads: 317381
Percentage reads mapped: 43.44
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5333 | p.Met32Leu | missense_variant | 0.14 |
gyrB | 6663 | p.Phe475Tyr | missense_variant | 0.19 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.22 |
gyrA | 6676 | c.-626T>C | upstream_gene_variant | 0.22 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.24 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.25 |
gyrA | 6724 | c.-578G>C | upstream_gene_variant | 0.25 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.25 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.22 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.22 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.22 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 0.23 |
gyrA | 6772 | c.-530C>G | upstream_gene_variant | 0.25 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.25 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.26 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.24 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.29 |
gyrA | 6805 | c.-497G>T | upstream_gene_variant | 0.31 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.31 |
gyrA | 6826 | c.-476G>C | upstream_gene_variant | 0.25 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.27 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.27 |
gyrA | 7012 | c.-290G>C | upstream_gene_variant | 0.2 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 0.2 |
gyrA | 7021 | c.-281G>C | upstream_gene_variant | 0.2 |
gyrA | 7024 | c.-278G>C | upstream_gene_variant | 0.2 |
gyrB | 7025 | p.Lys596Ala | missense_variant | 0.2 |
gyrA | 7030 | c.-272C>G | upstream_gene_variant | 0.2 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.2 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.2 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 0.2 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.19 |
gyrA | 7356 | p.Asp19His | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8610 | p.Asp437Tyr | missense_variant | 0.33 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 1.0 |
gyrA | 8669 | c.1368C>A | synonymous_variant | 0.25 |
fgd1 | 490669 | c.-114C>T | upstream_gene_variant | 0.15 |
fgd1 | 491005 | p.Leu75Met | missense_variant | 0.21 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.31 |
fgd1 | 491034 | c.252C>T | synonymous_variant | 0.18 |
fgd1 | 491037 | c.255C>G | synonymous_variant | 0.45 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.45 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.45 |
fgd1 | 491058 | c.276C>G | synonymous_variant | 0.45 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.45 |
fgd1 | 491067 | c.285C>T | synonymous_variant | 0.45 |
fgd1 | 491082 | c.300T>C | synonymous_variant | 0.23 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.23 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.23 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.23 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.23 |
fgd1 | 491112 | c.330G>C | synonymous_variant | 0.23 |
fgd1 | 491137 | c.356delA | frameshift_variant | 0.18 |
ccsA | 620045 | p.Gly52Ala | missense_variant | 0.4 |
rpoB | 759663 | c.-144G>A | upstream_gene_variant | 0.17 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.22 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.43 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.41 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.39 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.32 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.22 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.26 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.32 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.31 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.31 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.31 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.31 |
rpoB | 760317 | c.511_513delAGCinsTCG | synonymous_variant | 0.31 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.31 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.31 |
rpoB | 760334 | c.528G>C | synonymous_variant | 0.31 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.29 |
rpoB | 760353 | p.Glu183His | missense_variant | 0.33 |
rpoB | 760358 | c.552C>G | synonymous_variant | 0.33 |
rpoB | 760359 | p.Ile185Val | missense_variant | 0.33 |
rpoB | 760368 | p.Ser188Thr | missense_variant | 0.33 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.33 |
rpoB | 760380 | p.Thr192Asp | missense_variant | 0.32 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.5 |
rpoB | 760403 | c.597C>T | synonymous_variant | 0.5 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.55 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.48 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.6 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.57 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.63 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.63 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.63 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.57 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.61 |
rpoB | 760508 | c.702G>T | synonymous_variant | 0.62 |
rpoB | 760522 | p.Ser239Thr | missense_variant | 0.63 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.58 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.58 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.58 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.58 |
rpoB | 760553 | c.747C>G | synonymous_variant | 0.55 |
rpoB | 760557 | c.753_754insCTC | conservative_inframe_insertion | 0.55 |
rpoB | 760568 | c.762G>C | synonymous_variant | 0.55 |
rpoB | 760589 | c.783C>G | synonymous_variant | 0.53 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.53 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.5 |
rpoB | 760649 | c.843G>C | synonymous_variant | 0.38 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.33 |
rpoB | 760659 | c.853_855delTCAinsAGC | synonymous_variant | 0.22 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.22 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.24 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.24 |
rpoB | 760734 | p.Val310Ile | missense_variant | 0.13 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.21 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.21 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.21 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.32 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.32 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.48 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.45 |
rpoB | 760949 | c.1143C>T | synonymous_variant | 0.52 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.48 |
rpoB | 760961 | c.1155C>G | synonymous_variant | 0.48 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.52 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.56 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.65 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.65 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.63 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.64 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.62 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.54 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.54 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.55 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.52 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.56 |
rpoB | 761087 | c.1281C>G | synonymous_variant | 0.56 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.56 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.62 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.6 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.73 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.74 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.77 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.77 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.76 |
rpoB | 761174 | c.1368T>A | synonymous_variant | 0.72 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.72 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.74 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.73 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.73 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.75 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.8 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.79 |
rpoB | 761255 | c.1449T>C | synonymous_variant | 0.8 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.8 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.77 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.72 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 0.68 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.61 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.58 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.52 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.55 |
rpoB | 761355 | p.Val517Arg | missense_variant | 0.55 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.55 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.55 |
rpoB | 761370 | p.Ile522Val | missense_variant | 0.58 |
rpoB | 761374 | p.Val523Asp | missense_variant | 0.58 |
rpoB | 761387 | c.1581C>G | synonymous_variant | 0.58 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.33 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.33 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.23 |
rpoB | 761427 | p.Pro541Ser | missense_variant | 0.27 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.5 |
rpoB | 761540 | c.1734C>G | synonymous_variant | 0.5 |
rpoB | 761549 | c.1743G>C | synonymous_variant | 0.5 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.38 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.38 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.38 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.38 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.3 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.3 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.3 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.3 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.38 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.33 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.29 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.29 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.33 |
rpoB | 761661 | p.Leu619Ile | missense_variant | 0.29 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.29 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.22 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.22 |
rpoB | 761739 | p.Glu645* | stop_gained | 0.33 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.6 |
rpoB | 761819 | c.2013G>C | synonymous_variant | 0.6 |
rpoB | 761822 | c.2016C>G | synonymous_variant | 0.67 |
rpoB | 761828 | p.His674Gln | missense_variant | 0.71 |
rpoB | 761834 | c.2028T>G | synonymous_variant | 0.71 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.62 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.62 |
rpoB | 761863 | p.Ala686Glu | missense_variant | 0.5 |
rpoB | 761867 | c.2061C>T | synonymous_variant | 0.5 |
rpoB | 761868 | p.Asp688Gln | missense_variant | 0.5 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.5 |
rpoB | 761876 | c.2070C>G | synonymous_variant | 0.5 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.5 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.5 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.45 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.45 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.45 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.45 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.45 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.62 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.62 |
rpoB | 761955 | p.Ile717Val | missense_variant | 0.61 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.6 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.6 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.6 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.53 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.53 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.74 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.74 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.68 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.68 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.69 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.7 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 0.66 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.66 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.66 |
rpoB | 762119 | c.2313C>G | synonymous_variant | 0.66 |
rpoB | 762128 | c.2322G>T | synonymous_variant | 0.67 |
rpoB | 762134 | c.2328C>G | synonymous_variant | 0.67 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.68 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.68 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.69 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.68 |
rpoB | 762170 | c.2364C>G | synonymous_variant | 0.7 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.68 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 0.68 |
rpoB | 762185 | c.2379G>T | synonymous_variant | 0.66 |
rpoB | 762189 | p.Ile795Val | missense_variant | 0.64 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.6 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.62 |
rpoB | 762230 | c.2424G>C | synonymous_variant | 0.52 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.52 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.52 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.6 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.62 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.62 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.61 |
rpoB | 762275 | c.2469C>G | synonymous_variant | 0.67 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.72 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.81 |
rpoB | 762318 | p.Ser838Asn | missense_variant | 0.81 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.79 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.78 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.78 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.77 |
rpoB | 762350 | c.2544C>G | synonymous_variant | 0.77 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.74 |
rpoB | 762368 | p.Glu854Asp | missense_variant | 0.69 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.69 |
rpoC | 762374 | c.-996G>T | upstream_gene_variant | 0.69 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.69 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.69 |
rpoC | 762383 | c.-987C>G | upstream_gene_variant | 0.69 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.58 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.58 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.65 |
rpoC | 762407 | c.-963G>C | upstream_gene_variant | 0.65 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.65 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.61 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 0.69 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.69 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.73 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.73 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.67 |
rpoC | 762485 | c.-885G>C | upstream_gene_variant | 0.62 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.62 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.29 |
rpoB | 762510 | p.Ala902Ser | missense_variant | 0.29 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.25 |
rpoB | 762525 | p.Val907Ile | missense_variant | 0.25 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.25 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.25 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.25 |
rpoC | 762545 | c.-825C>G | upstream_gene_variant | 0.25 |
rpoC | 762554 | c.-816G>C | upstream_gene_variant | 0.25 |
rpoB | 762729 | p.Gln975Lys | missense_variant | 0.38 |
rpoB | 762736 | p.Ala977Asp | missense_variant | 0.42 |
rpoB | 762744 | p.Gln980Thr | missense_variant | 0.42 |
rpoC | 762749 | c.-621C>T | upstream_gene_variant | 0.42 |
rpoC | 762753 | c.-617T>C | upstream_gene_variant | 0.42 |
rpoB | 762759 | p.Cys985Ser | missense_variant | 0.42 |
rpoB | 762765 | p.Leu987Ile | missense_variant | 0.42 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.36 |
rpoC | 762785 | c.-585C>T | upstream_gene_variant | 0.36 |
rpoB | 762786 | p.Val994Gln | missense_variant | 0.36 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.36 |
rpoB | 762796 | p.Asp997Gly | missense_variant | 0.36 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.41 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.47 |
rpoC | 762827 | c.-543G>T | upstream_gene_variant | 0.5 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.5 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.44 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.44 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.44 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.46 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.52 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.54 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.54 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.54 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.52 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.5 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.52 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.48 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.48 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.5 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.48 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.46 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.46 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.5 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.5 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.59 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.59 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.59 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.64 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.57 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.57 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.57 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.57 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.53 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.5 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.45 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.33 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 0.33 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 0.33 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.23 |
rpoC | 763392 | p.Asp8Val | missense_variant | 0.22 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.44 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.44 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.44 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.5 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.44 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.55 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.55 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.58 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.59 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.71 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.76 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.76 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.77 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.68 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.68 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.69 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.65 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.68 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.68 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.69 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.71 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.72 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.78 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.78 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.8 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.78 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.78 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.74 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.71 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.71 |
rpoC | 763786 | c.417C>G | synonymous_variant | 0.74 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.7 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.7 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.69 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.62 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.58 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.54 |
rpoC | 763836 | p.Ala156Glu | missense_variant | 0.48 |
rpoC | 763840 | c.471G>C | synonymous_variant | 0.46 |
rpoC | 763844 | p.Arg159Lys | missense_variant | 0.46 |
rpoC | 763857 | p.Glu163Ala | missense_variant | 0.48 |
rpoC | 763861 | c.492C>T | synonymous_variant | 0.48 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.46 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.5 |
rpoC | 763879 | c.510A>C | synonymous_variant | 0.53 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.55 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.53 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.55 |
rpoC | 763906 | c.537C>G | synonymous_variant | 0.54 |
rpoC | 763910 | p.Leu181Ile | missense_variant | 0.46 |
rpoC | 763921 | c.552G>C | synonymous_variant | 0.42 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.43 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 0.43 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.45 |
rpoC | 763947 | p.Ala193Val | missense_variant | 0.43 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.41 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.41 |
rpoC | 763961 | p.Arg198Lys | missense_variant | 0.41 |
rpoC | 763966 | c.597C>T | synonymous_variant | 0.41 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.39 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.38 |
rpoC | 764020 | c.651C>T | synonymous_variant | 0.28 |
rpoC | 764023 | c.654G>T | synonymous_variant | 0.19 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.19 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.25 |
rpoC | 764039 | c.670_671delAGinsTC | synonymous_variant | 0.22 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.33 |
rpoC | 764062 | c.693C>G | synonymous_variant | 0.21 |
rpoC | 764071 | c.702G>C | synonymous_variant | 0.23 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.35 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.33 |
rpoC | 764128 | c.759C>G | synonymous_variant | 0.45 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.45 |
rpoC | 764134 | c.765C>G | synonymous_variant | 0.53 |
rpoC | 764149 | c.780G>C | synonymous_variant | 0.56 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.56 |
rpoC | 764164 | p.Ile265Met | missense_variant | 0.56 |
rpoC | 764169 | p.Asn267Thr | missense_variant | 0.58 |
rpoC | 764182 | p.Asp271Glu | missense_variant | 0.61 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.52 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.57 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.57 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.57 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.6 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.6 |
rpoC | 764239 | c.870T>C | synonymous_variant | 0.68 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.65 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.65 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.65 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.65 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.65 |
rpoC | 764275 | c.909_911delACA | disruptive_inframe_deletion | 0.63 |
rpoC | 764302 | c.933C>G | synonymous_variant | 0.58 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.63 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.62 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.62 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.65 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.64 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.62 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.56 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.56 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.5 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.47 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.47 |
rpoC | 764425 | c.1056C>T | synonymous_variant | 0.41 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.38 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.4 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.4 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.4 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.47 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.47 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.58 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.58 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.44 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.47 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.53 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.41 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.44 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.41 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.44 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.44 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.5 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.55 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.68 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.7 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.62 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.62 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.63 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.56 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.57 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.59 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.62 |
rpoC | 764707 | c.1338G>C | synonymous_variant | 0.68 |
rpoC | 764713 | c.1344G>A | synonymous_variant | 0.62 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.62 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.66 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.65 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.65 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.67 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.69 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.72 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.72 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.71 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.74 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.74 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.74 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.73 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.71 |
rpoC | 764844 | p.Ala492Gly | missense_variant | 0.68 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.68 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.6 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 0.42 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.36 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.38 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.38 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.38 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.3 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.3 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.3 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.3 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.27 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.27 |
rpoC | 765098 | p.Pro577Thr | missense_variant | 0.22 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.21 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.2 |
rpoC | 765404 | p.Leu679Ala | missense_variant | 0.27 |
rpoC | 765407 | p.Gly680Asn | missense_variant | 0.27 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.27 |
rpoC | 765425 | p.Lys686Glu | missense_variant | 0.3 |
rpoC | 765435 | p.His689Pro | missense_variant | 0.25 |
rpoC | 765443 | p.Val692Arg | missense_variant | 0.25 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.25 |
rpoC | 765452 | p.Ala695Thr | missense_variant | 0.25 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.21 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.19 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.18 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 0.23 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.23 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.23 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.25 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.25 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.23 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.33 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.33 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.38 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.38 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.39 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.37 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.43 |
rpoC | 766428 | c.3059_3060insGGC | disruptive_inframe_insertion | 0.38 |
rpoC | 766432 | c.3063T>C | synonymous_variant | 0.43 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.43 |
rpoC | 766459 | c.3090G>C | synonymous_variant | 0.29 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.25 |
rpoC | 766480 | c.3111C>T | synonymous_variant | 0.14 |
rpoC | 766483 | c.3114G>T | synonymous_variant | 0.14 |
rpoC | 766490 | p.Arg1041Asn | missense_variant | 0.14 |
rpoC | 766504 | c.3135G>C | synonymous_variant | 0.18 |
rpoC | 766510 | c.3141C>G | synonymous_variant | 0.18 |
rpoC | 766517 | p.Thr1050Ser | missense_variant | 0.2 |
rpoC | 766522 | c.3153C>T | synonymous_variant | 0.2 |
rpoC | 766525 | c.3156G>C | synonymous_variant | 0.2 |
rpoC | 766526 | p.Val1053Ile | missense_variant | 0.2 |
rpoC | 766530 | p.Arg1054Gln | missense_variant | 0.18 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.22 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.2 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.2 |
rpoC | 766546 | p.Glu1059Asp | missense_variant | 0.2 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.43 |
rpoC | 766573 | c.3204T>G | synonymous_variant | 0.43 |
rpoC | 766579 | c.3210C>T | synonymous_variant | 0.5 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.5 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.5 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.5 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.54 |
rpoC | 766612 | c.3243C>G | synonymous_variant | 0.58 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.58 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 0.58 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.55 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.44 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.38 |
rpoC | 766652 | p.Ser1095Thr | missense_variant | 0.38 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.43 |
rpoC | 766660 | c.3291G>C | synonymous_variant | 0.43 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.43 |
rpoC | 766664 | c.3295_3297delCTCinsTTG | synonymous_variant | 0.43 |
rpoC | 766669 | c.3300C>G | synonymous_variant | 0.43 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.43 |
rpoC | 766684 | c.3315C>G | synonymous_variant | 0.5 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.5 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.6 |
rpoC | 766711 | c.3342C>T | synonymous_variant | 0.6 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.6 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.75 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.75 |
rpoC | 766732 | c.3363G>C | synonymous_variant | 0.75 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.67 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.67 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.78 |
rpoC | 766810 | c.3441G>T | synonymous_variant | 0.15 |
rpoC | 766813 | c.3444G>C | synonymous_variant | 0.85 |
rpoC | 766835 | p.Val1156Thr | missense_variant | 0.76 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.76 |
rpoC | 766855 | c.3486G>C | synonymous_variant | 0.65 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.65 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.62 |
rpoC | 766885 | c.3516G>C | synonymous_variant | 0.6 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.56 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.56 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.53 |
rpoC | 766903 | c.3534C>A | synonymous_variant | 0.53 |
rpoC | 766911 | p.Ile1181Thr | missense_variant | 0.53 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.53 |
rpoC | 766919 | p.Ala1184Ser | missense_variant | 0.59 |
rpoC | 766932 | c.3564delA | frameshift_variant | 0.56 |
rpoC | 766936 | c.3567_3568insC | frameshift_variant | 0.5 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.53 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.53 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.55 |
rpoC | 766952 | p.Ala1195Ser | missense_variant | 0.55 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.65 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.68 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.64 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.8 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.79 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.78 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.72 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.75 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.81 |
rpoC | 767093 | c.3724_3726delAGCinsTCG | synonymous_variant | 0.81 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.81 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.81 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.81 |
rpoC | 767113 | c.3744G>C | synonymous_variant | 0.83 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.83 |
rpoC | 767152 | c.3783T>C | synonymous_variant | 0.81 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.81 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.8 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.8 |
rpoC | 767180 | p.Ala1271Thr | missense_variant | 0.76 |
rpoC | 767203 | c.3834C>A | synonymous_variant | 0.6 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.62 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.62 |
rpoC | 767215 | c.3846G>C | synonymous_variant | 0.62 |
rpoC | 767219 | p.Thr1284Ala | missense_variant | 0.62 |
rpoC | 767222 | p.Ile1285Val | missense_variant | 0.62 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.71 |
rpoC | 767236 | p.Glu1289Asp | missense_variant | 0.71 |
mmpL5 | 776525 | p.Met652Ile | missense_variant | 0.2 |
mmpL5 | 778189 | p.Gln98* | stop_gained | 0.2 |
mmpL5 | 778920 | c.-440C>A | upstream_gene_variant | 0.29 |
mmpL5 | 779121 | c.-641C>T | upstream_gene_variant | 0.17 |
mmpL5 | 779196 | c.-716G>T | upstream_gene_variant | 0.33 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.19 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.19 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.22 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.27 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.29 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.32 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.33 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.35 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.33 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.32 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.3 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.33 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.33 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.29 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.3 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.35 |
rplC | 800666 | c.-143C>T | upstream_gene_variant | 0.15 |
rplC | 800669 | c.-140G>T | upstream_gene_variant | 0.15 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.17 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.21 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.21 |
fbiC | 1304646 | c.1716T>G | synonymous_variant | 0.25 |
fbiC | 1304651 | p.Ala574Glu | missense_variant | 0.25 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.25 |
fbiC | 1304660 | p.Tyr577Phe | missense_variant | 0.25 |
fbiC | 1304667 | c.1737G>C | synonymous_variant | 0.25 |
fbiC | 1304672 | p.Val581Ala | missense_variant | 0.25 |
fbiC | 1304674 | p.Gly582Ser | missense_variant | 0.25 |
fbiC | 1304682 | c.1752C>G | synonymous_variant | 0.27 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.3 |
fbiC | 1304709 | c.1779C>T | synonymous_variant | 0.25 |
fbiC | 1304710 | p.Ala594Leu | missense_variant | 0.25 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.25 |
fbiC | 1304718 | c.1788C>G | synonymous_variant | 0.25 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.23 |
fbiC | 1304727 | c.1797A>C | synonymous_variant | 0.23 |
Rv1258c | 1406188 | c.1153C>T | synonymous_variant | 0.25 |
Rv1258c | 1407280 | p.Ala21Ser | missense_variant | 0.33 |
embR | 1416997 | c.351C>T | synonymous_variant | 0.18 |
embR | 1417186 | c.162C>A | synonymous_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472027 | n.182C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472040 | n.195T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472057 | n.212C>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472449 | n.604C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472463 | n.618G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472495 | n.650C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472497 | n.652G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472580 | n.735C>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472851 | n.1006A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472856 | n.1011T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472858 | n.1013G>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472861 | n.1016G>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472862 | n.1017T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472863 | n.1018T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472971 | n.1126G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473673 | n.16G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474292 | n.636_642delTCCTCTC | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474303 | n.646A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474413 | n.757_767delCCCACACGCGC | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474662 | n.1005C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474688 | n.1031G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474712 | n.1055G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474823 | n.1166C>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474904 | n.1247G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475201 | n.1544G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475222 | n.1565G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475337 | n.1680C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475339 | n.1682T>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475340 | n.1683A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475353 | n.1696A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475354 | n.1697A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475361 | n.1704G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475376 | n.1719A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475379 | n.1722G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475382 | n.1725A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475395 | n.1738T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475398 | n.1741C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475614 | n.1957A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475618 | n.1961C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475633 | n.1976G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475636 | n.1979A>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476091 | n.2434_2435insC | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1674172 | p.Met245Val | missense_variant | 0.2 |
rpsA | 1833571 | c.30A>G | synonymous_variant | 0.25 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.25 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.2 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.2 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.22 |
rpsA | 1833607 | c.66T>C | synonymous_variant | 0.22 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.22 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.22 |
rpsA | 1833623 | p.Lys28Ala | missense_variant | 0.25 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.27 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.27 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.27 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.27 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.27 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.27 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.27 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.33 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.33 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.44 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.44 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.44 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.44 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.5 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.53 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.53 |
rpsA | 1833805 | c.264C>T | synonymous_variant | 0.55 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.55 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.55 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.73 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.62 |
rpsA | 1833838 | c.297G>A | synonymous_variant | 0.62 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.62 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.59 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.56 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.56 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.56 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.57 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.73 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.65 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.63 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.61 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.61 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.61 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.61 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.61 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.61 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.58 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.58 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.62 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.62 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.59 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.59 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.59 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.58 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.57 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.5 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.5 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.42 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.38 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.27 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.27 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.33 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.33 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.33 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.27 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.27 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.27 |
rpsA | 1834192 | c.651C>G | synonymous_variant | 0.27 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.27 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.18 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.18 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.26 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.29 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.29 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.27 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.27 |
rpsA | 1834307 | p.Asp256Thr | missense_variant | 0.27 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.35 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.35 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.35 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.33 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.33 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.33 |
rpsA | 1834361 | c.820_822delTTGinsCTC | synonymous_variant | 0.33 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.33 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.36 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.44 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.44 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.44 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.44 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.45 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.57 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.59 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.57 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.57 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.48 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.56 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.56 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.53 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.53 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.53 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.53 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.53 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 0.53 |
rpsA | 1834570 | c.1029C>T | synonymous_variant | 0.56 |
rpsA | 1834574 | p.Met345Leu | missense_variant | 0.56 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.6 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.56 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.56 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.5 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.5 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.45 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.48 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.5 |
rpsA | 1834650 | p.Thr370Ser | missense_variant | 0.44 |
rpsA | 1834653 | p.Glu371Ala | missense_variant | 0.5 |
rpsA | 1834663 | c.1122C>T | synonymous_variant | 0.5 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.5 |
rpsA | 1834688 | c.1147_1149delAGTinsTCG | synonymous_variant | 0.46 |
rpsA | 1834712 | p.Ile391Val | missense_variant | 0.54 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.5 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.5 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.5 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 0.5 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.5 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.5 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.45 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.4 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.4 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.44 |
rpsA | 1834788 | p.Ala416Gly | missense_variant | 0.44 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.36 |
rpsA | 1834813 | c.1272G>T | synonymous_variant | 0.4 |
rpsA | 1834831 | c.1290G>T | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918085 | p.Thr49Ile | missense_variant | 0.17 |
tlyA | 1918088 | p.Thr50Ile | missense_variant | 0.17 |
ndh | 2101862 | p.Leu394Pro | missense_variant | 0.33 |
ndh | 2103050 | c.-8A>T | upstream_gene_variant | 0.5 |
PPE35 | 2168290 | p.Thr775Ser | missense_variant | 0.2 |
PPE35 | 2169309 | p.Gly435Asp | missense_variant | 0.22 |
PPE35 | 2169397 | p.Gly406Ser | missense_variant | 0.4 |
PPE35 | 2169752 | c.861C>T | synonymous_variant | 0.2 |
PPE35 | 2170155 | p.Ala153Gly | missense_variant | 0.25 |
PPE35 | 2170157 | c.456G>C | synonymous_variant | 0.25 |
PPE35 | 2170653 | c.-41C>A | upstream_gene_variant | 0.18 |
Rv1979c | 2221926 | c.1239C>T | synonymous_variant | 0.2 |
Rv1979c | 2222229 | p.Met312Ile | missense_variant | 0.15 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.27 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.22 |
kasA | 2517965 | c.-150C>G | upstream_gene_variant | 0.33 |
kasA | 2517966 | c.-149G>A | upstream_gene_variant | 0.33 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.25 |
kasA | 2517988 | c.-127_-126delTTinsCC | upstream_gene_variant | 0.25 |
kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.25 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.25 |
eis | 2715496 | c.-164C>A | upstream_gene_variant | 0.22 |
eis | 2715549 | c.-217G>A | upstream_gene_variant | 0.15 |
ahpC | 2726415 | p.Phe75Leu | missense_variant | 0.2 |
folC | 2747681 | c.-83G>T | upstream_gene_variant | 0.17 |
ribD | 2986896 | p.Val20Leu | missense_variant | 0.4 |
Rv2752c | 3065025 | c.1167G>A | synonymous_variant | 0.18 |
Rv2752c | 3067006 | c.-816delC | upstream_gene_variant | 0.25 |
thyX | 3067714 | p.Val78Leu | missense_variant | 0.4 |
thyA | 3074184 | c.288A>G | synonymous_variant | 0.15 |
ald | 3087220 | p.Ser134Ile | missense_variant | 0.67 |
fbiD | 3339098 | c.-20G>T | upstream_gene_variant | 0.17 |
Rv3083 | 3448674 | c.171C>T | synonymous_variant | 0.18 |
Rv3083 | 3448785 | c.282C>A | synonymous_variant | 0.25 |
Rv3083 | 3449544 | c.1041T>C | synonymous_variant | 0.18 |
Rv3083 | 3449833 | p.Val444Met | missense_variant | 0.17 |
whiB7 | 3568877 | c.-198C>T | upstream_gene_variant | 0.14 |
fbiA | 3640682 | p.Val47Gly | missense_variant | 0.18 |
fbiA | 3641176 | p.Ala212Ser | missense_variant | 0.18 |
fbiA | 3641417 | p.Asp292Val | missense_variant | 0.22 |
fbiB | 3641672 | c.138G>T | synonymous_variant | 0.18 |
alr | 3841507 | c.-87C>T | upstream_gene_variant | 0.25 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.33 |
rpoA | 3877590 | c.918G>C | synonymous_variant | 0.33 |
rpoA | 3877596 | c.912G>C | synonymous_variant | 0.33 |
rpoA | 3877600 | p.Gln303Ser | missense_variant | 0.33 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.44 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.44 |
rpoA | 3877638 | c.870T>A | synonymous_variant | 0.41 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.5 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.5 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.5 |
rpoA | 3877677 | p.Ala277Gly | missense_variant | 0.5 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.47 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.47 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.5 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.58 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.48 |
rpoA | 3877740 | c.768G>C | synonymous_variant | 0.43 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.45 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.48 |
rpoA | 3877764 | p.Ala248Gly | missense_variant | 0.48 |
rpoA | 3877770 | c.738A>C | synonymous_variant | 0.48 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.48 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.46 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.46 |
rpoA | 3877794 | c.714G>C | synonymous_variant | 0.5 |
rpoA | 3877800 | c.708G>C | synonymous_variant | 0.52 |
rpoA | 3877803 | c.705G>A | synonymous_variant | 0.54 |
rpoA | 3877821 | c.687C>A | synonymous_variant | 0.5 |
rpoA | 3877824 | c.684G>A | synonymous_variant | 0.5 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.48 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.46 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 0.46 |
rpoA | 3877848 | c.660C>G | synonymous_variant | 0.46 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.5 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.43 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.43 |
rpoA | 3877881 | c.627G>T | synonymous_variant | 0.43 |
rpoA | 3877884 | c.624G>C | synonymous_variant | 0.43 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 0.44 |
rpoA | 3877896 | p.Pro204Ala | missense_variant | 0.44 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.44 |
rpoA | 3877905 | c.603A>C | synonymous_variant | 0.44 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.44 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.5 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.44 |
rpoA | 3877932 | c.576G>C | synonymous_variant | 0.47 |
rpoA | 3877936 | p.Lys191Arg | missense_variant | 0.47 |
rpoA | 3877938 | c.570C>T | synonymous_variant | 0.47 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.53 |
rpoA | 3877965 | c.543C>T | synonymous_variant | 0.56 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.6 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.67 |
rpoA | 3877998 | c.510G>C | synonymous_variant | 0.58 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.58 |
rpoA | 3878010 | c.498C>G | synonymous_variant | 0.55 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.6 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.6 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.55 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.55 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.67 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.6 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.5 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.5 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.5 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.5 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.46 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.46 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.38 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.4 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.47 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.43 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.43 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.43 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.41 |
rpoA | 3878124 | c.384G>C | synonymous_variant | 0.41 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.41 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.41 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.41 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.41 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.41 |
rpoA | 3878153 | p.His119Asn | missense_variant | 0.5 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.56 |
rpoA | 3878196 | p.Glu104Thr | missense_variant | 0.53 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.53 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.53 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.5 |
rpoA | 3878244 | p.Glu88Asp | missense_variant | 0.52 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.52 |
rpoA | 3878251 | c.256_257delTCinsAG | synonymous_variant | 0.55 |
rpoA | 3878256 | c.252G>T | synonymous_variant | 0.55 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.55 |
rpoA | 3878262 | p.Ser82Gly | missense_variant | 0.55 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.61 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.61 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.61 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.61 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.61 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.59 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.53 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.43 |
rpoA | 3878331 | c.177A>C | synonymous_variant | 0.33 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.33 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.33 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.27 |
rpoA | 3878358 | c.150C>T | synonymous_variant | 0.3 |
rpoA | 3878361 | c.147G>C | synonymous_variant | 0.3 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.3 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.3 |
rpoA | 3878379 | c.129G>C | synonymous_variant | 0.3 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.27 |
rpoA | 3878394 | c.114G>C | synonymous_variant | 0.27 |
rpoA | 3878406 | c.102G>C | synonymous_variant | 0.3 |
rpoA | 3878415 | c.93C>G | synonymous_variant | 0.22 |
clpC1 | 4038446 | p.Asp753Glu | missense_variant | 0.15 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.33 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.36 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.33 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.45 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.45 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.48 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.52 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.5 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.54 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.54 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.52 |
clpC1 | 4038860 | c.1845G>T | synonymous_variant | 0.5 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.53 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.57 |
clpC1 | 4038896 | c.1809C>T | synonymous_variant | 0.59 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.57 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.53 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.52 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.48 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.47 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.47 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.5 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.55 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.56 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.61 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.52 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.53 |
clpC1 | 4038977 | c.1728G>C | synonymous_variant | 0.53 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.58 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.57 |
clpC1 | 4038995 | c.1708_1710delTTGinsCTC | synonymous_variant | 0.57 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.58 |
clpC1 | 4039010 | c.1695G>C | synonymous_variant | 0.61 |
clpC1 | 4039016 | c.1689C>G | synonymous_variant | 0.57 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.55 |
clpC1 | 4039040 | c.1665C>G | synonymous_variant | 0.56 |
clpC1 | 4039043 | c.1662G>C | synonymous_variant | 0.56 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.59 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.58 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.54 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.54 |
clpC1 | 4039106 | c.1599G>T | synonymous_variant | 0.55 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.57 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.57 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.57 |
clpC1 | 4039136 | p.Asp523Glu | missense_variant | 0.5 |
clpC1 | 4039139 | p.Glu522Val | missense_variant | 0.4 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.4 |
clpC1 | 4039145 | c.1560G>T | synonymous_variant | 0.4 |
clpC1 | 4039154 | c.1551G>C | synonymous_variant | 0.4 |
clpC1 | 4039163 | c.1542G>C | synonymous_variant | 0.4 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.35 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.4 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.4 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.4 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.4 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.4 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.43 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.4 |
clpC1 | 4039244 | c.1461G>C | synonymous_variant | 0.38 |
clpC1 | 4039258 | p.Gln483Glu | missense_variant | 0.25 |
clpC1 | 4039259 | p.Glu482Asn | missense_variant | 0.25 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.3 |
clpC1 | 4039279 | p.Val476Ile | missense_variant | 0.3 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.3 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.29 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.31 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.33 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.33 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.38 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.41 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.41 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.41 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.41 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.44 |
clpC1 | 4039347 | p.Arg453Lys | missense_variant | 0.52 |
clpC1 | 4039359 | p.Ser449Asn | missense_variant | 0.52 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.52 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.59 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.52 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.52 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.54 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.48 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.46 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 0.5 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.5 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.41 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.31 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.29 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.31 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.32 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.32 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.32 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.32 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.32 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.32 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.4 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.4 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.4 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.4 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.4 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.4 |
clpC1 | 4039574 | c.1131G>A | synonymous_variant | 0.38 |
clpC1 | 4039575 | c.1128_1129delTG | frameshift_variant | 0.35 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.36 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.36 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.41 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.37 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.38 |
clpC1 | 4039646 | p.Glu353Asp | missense_variant | 0.56 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.56 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.62 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.62 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.68 |
clpC1 | 4039694 | c.1011G>A | synonymous_variant | 0.69 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.74 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.77 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.77 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.76 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.79 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.79 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.79 |
clpC1 | 4039763 | c.942C>T | synonymous_variant | 0.79 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.79 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.71 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.68 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.58 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.58 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.58 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.58 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.58 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.64 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.55 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.54 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.54 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.55 |
clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.55 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.5 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.5 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.5 |
clpC1 | 4039942 | c.763C>T | synonymous_variant | 0.48 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.45 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.45 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.48 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.48 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.48 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.46 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.52 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.5 |
clpC1 | 4039991 | c.714G>T | synonymous_variant | 0.52 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.54 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.5 |
clpC1 | 4040015 | c.690G>A | synonymous_variant | 0.48 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.48 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.48 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.48 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.48 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.43 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.4 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.4 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.43 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.47 |
clpC1 | 4040108 | c.597G>T | synonymous_variant | 0.47 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.47 |
clpC1 | 4040124 | p.Glu194Ser | missense_variant | 0.43 |
clpC1 | 4040141 | c.564C>T | synonymous_variant | 0.3 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.2 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.2 |
clpC1 | 4040180 | c.525C>A | synonymous_variant | 0.2 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.22 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.22 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.22 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.29 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.29 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.29 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.22 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.35 |
clpC1 | 4040336 | c.369G>C | synonymous_variant | 0.32 |
clpC1 | 4040348 | c.357G>C | synonymous_variant | 0.4 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.36 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.36 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.35 |
clpC1 | 4040366 | c.339C>T | synonymous_variant | 0.35 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.35 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.35 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.38 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.44 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.48 |
clpC1 | 4040408 | c.297C>A | synonymous_variant | 0.52 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.52 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.48 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.48 |
clpC1 | 4040429 | c.274_276delTTGinsCTC | synonymous_variant | 0.47 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 0.48 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.52 |
clpC1 | 4040456 | c.249C>T | synonymous_variant | 0.52 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.52 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.52 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.59 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.55 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.48 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.38 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.38 |
clpC1 | 4040549 | c.154_156delTTGinsCTC | synonymous_variant | 0.37 |
clpC1 | 4040561 | c.144A>C | synonymous_variant | 0.31 |
clpC1 | 4040567 | c.138C>G | synonymous_variant | 0.25 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.25 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.21 |
clpC1 | 4040582 | c.123G>T | synonymous_variant | 0.27 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.26 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.26 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.26 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.24 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.24 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.26 |
clpC1 | 4040615 | c.90C>G | synonymous_variant | 0.29 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.31 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.25 |
clpC1 | 4040657 | c.48T>C | synonymous_variant | 0.25 |
embC | 4240447 | c.585G>C | synonymous_variant | 0.22 |
embC | 4241878 | c.2016G>A | synonymous_variant | 0.25 |
embC | 4242341 | p.Thr827Ala | missense_variant | 0.18 |
embC | 4242398 | p.Ala846Ser | missense_variant | 0.18 |
embA | 4243366 | p.Trp45* | stop_gained | 0.29 |
embA | 4243983 | p.Arg251Trp | missense_variant | 0.2 |
embA | 4245024 | p.His598Tyr | missense_variant | 0.22 |
embA | 4245796 | p.Ala855Val | missense_variant | 0.15 |
embA | 4246194 | p.Pro988Thr | missense_variant | 0.14 |
embB | 4249011 | p.Leu833Gln | missense_variant | 0.17 |
embB | 4249226 | p.Pro905Ser | missense_variant | 0.22 |
aftB | 4267025 | c.1812C>T | synonymous_variant | 0.25 |
aftB | 4267105 | p.Val578Leu | missense_variant | 0.14 |
aftB | 4267433 | c.1404C>T | synonymous_variant | 0.17 |
ethR | 4326670 | c.-879G>A | upstream_gene_variant | 0.18 |
ethR | 4326748 | c.-801G>A | upstream_gene_variant | 0.15 |
ethR | 4327777 | p.Asp77Tyr | missense_variant | 0.17 |
ethR | 4327999 | p.Ala151Ser | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338619 | c.-99delG | upstream_gene_variant | 0.2 |
gid | 4407783 | c.420C>T | synonymous_variant | 0.25 |