Run ID: ERR2229542
Sample name:
Date: 31-03-2023 17:18:19
Number of reads: 1147201
Percentage reads mapped: 71.55
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.57 | streptomycin |
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6123 | p.Ala295Gly | missense_variant | 0.16 |
gyrB | 6196 | c.957C>T | synonymous_variant | 0.16 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.26 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.28 |
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.25 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.26 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.27 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.21 |
gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.19 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.18 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.17 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.17 |
gyrA | 6622 | c.-680C>T | upstream_gene_variant | 0.2 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.2 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.19 |
gyrA | 6640 | c.-662A>G | upstream_gene_variant | 0.18 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.19 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.25 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.23 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.26 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.23 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.25 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.3 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.33 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.29 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.26 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.29 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.2 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.16 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.18 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.18 |
gyrA | 7075 | c.-227T>C | upstream_gene_variant | 0.16 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.16 |
gyrA | 7093 | c.-209T>G | upstream_gene_variant | 0.15 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.19 |
gyrA | 7147 | c.-155G>C | upstream_gene_variant | 0.23 |
gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.27 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.19 |
gyrA | 7186 | c.-116C>G | upstream_gene_variant | 0.17 |
gyrA | 7234 | c.-68C>T | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.15 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.17 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.31 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.33 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.36 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.35 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.21 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.16 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.17 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.23 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.22 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.28 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.28 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.23 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.21 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.2 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.19 |
gyrA | 7607 | c.306C>T | synonymous_variant | 0.24 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.18 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.18 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.22 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.22 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.22 |
gyrA | 7658 | c.357A>C | synonymous_variant | 0.21 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.22 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.23 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.22 |
gyrA | 7685 | c.384G>A | synonymous_variant | 0.16 |
gyrA | 7688 | c.387C>T | synonymous_variant | 0.17 |
gyrA | 7853 | c.552C>G | synonymous_variant | 0.15 |
gyrA | 7858 | p.Ala186Glu | missense_variant | 0.15 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.18 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.21 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.17 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.29 |
gyrA | 8093 | c.792C>T | synonymous_variant | 0.29 |
gyrA | 8096 | c.795T>A | synonymous_variant | 0.3 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.3 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.26 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.27 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.28 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.27 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.27 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.33 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.34 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.29 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.27 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.2 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.22 |
gyrA | 8234 | c.933T>C | synonymous_variant | 0.24 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.27 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.32 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.29 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.29 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.26 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.24 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.21 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.22 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.28 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.2 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.2 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.19 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.19 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 0.17 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.17 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.15 |
gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 0.19 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.17 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.21 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.23 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.18 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.19 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.21 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.16 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.17 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.19 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.17 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.25 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 0.25 |
gyrA | 9104 | c.1803C>G | synonymous_variant | 0.26 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.33 |
gyrA | 9122 | c.1821C>G | synonymous_variant | 0.31 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.33 |
gyrA | 9152 | c.1851C>T | synonymous_variant | 0.33 |
gyrA | 9153 | p.Thr618Glu | missense_variant | 0.33 |
gyrA | 9158 | c.1857C>T | synonymous_variant | 0.36 |
gyrA | 9161 | c.1860C>G | synonymous_variant | 0.36 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.26 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.28 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.34 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.35 |
gyrA | 9224 | c.1923C>T | synonymous_variant | 0.22 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.23 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.22 |
gyrA | 9239 | c.1938C>T | synonymous_variant | 0.21 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.26 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.25 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.22 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.24 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.23 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.23 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.23 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.23 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.19 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.22 |
fgd1 | 491130 | c.348C>G | synonymous_variant | 0.22 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.35 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.36 |
fgd1 | 491173 | c.391C>A | synonymous_variant | 0.24 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.22 |
fgd1 | 491184 | c.402A>G | synonymous_variant | 0.23 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.19 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.19 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.22 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.22 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.25 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.26 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.28 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.24 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.25 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.24 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.17 |
mshA | 575665 | c.318G>A | synonymous_variant | 0.15 |
mshA | 575674 | c.327G>C | synonymous_variant | 0.19 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.23 |
mshA | 575701 | c.354G>A | synonymous_variant | 0.21 |
mshA | 575704 | c.357T>G | synonymous_variant | 0.21 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.22 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.19 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.2 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.18 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.33 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.34 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.36 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.39 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.39 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.42 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.36 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.34 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.36 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.34 |
mshA | 575905 | c.558G>C | synonymous_variant | 0.2 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.21 |
mshA | 575917 | p.Asp190Glu | missense_variant | 0.21 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.21 |
mshA | 575924 | p.Gly193Ser | missense_variant | 0.22 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.23 |
mshA | 575950 | c.603C>G | synonymous_variant | 0.23 |
mshA | 575959 | c.612G>A | synonymous_variant | 0.22 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
mshA | 576163 | c.816A>C | synonymous_variant | 0.18 |
mshA | 576166 | c.819C>G | synonymous_variant | 0.18 |
ccsA | 619697 | c.-194_-192delAGGinsCGC | upstream_gene_variant | 0.19 |
ccsA | 620310 | c.420C>T | synonymous_variant | 0.18 |
ccsA | 620317 | p.Val143Leu | missense_variant | 0.19 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.25 |
ccsA | 620346 | c.456C>G | synonymous_variant | 0.23 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.23 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.25 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.29 |
ccsA | 620376 | c.486G>C | synonymous_variant | 0.29 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.24 |
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 | 620460 | c.570T>G | synonymous_variant | 0.18 |
ccsA | 620461 | p.Val191Ile | missense_variant | 0.18 |
ccsA | 620682 | c.792G>A | synonymous_variant | 0.21 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.21 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.18 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.26 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.27 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.27 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.24 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.24 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.24 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.27 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.25 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.27 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.27 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.29 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.26 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.31 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.4 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.42 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.39 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.36 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.35 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.35 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.42 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.38 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.34 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.29 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.29 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.23 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.23 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.17 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.17 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.17 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.24 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.26 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.19 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.27 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.27 |
rpoB | 760598 | c.792C>A | synonymous_variant | 0.27 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.35 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.26 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.25 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.25 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.18 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.2 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.18 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.27 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.28 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.26 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.26 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.27 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.27 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.27 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.3 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.28 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.36 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.41 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.42 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.45 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.4 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.45 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.44 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.44 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.42 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.47 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.44 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.31 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.3 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.3 |
rpoB | 761373 | p.Val523His | missense_variant | 0.36 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.31 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.31 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.27 |
rpoB | 761438 | c.1632G>C | synonymous_variant | 0.17 |
rpoB | 761439 | p.Asp545Lys | missense_variant | 0.17 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.18 |
rpoB | 761452 | p.Val549Glu | missense_variant | 0.16 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.17 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.18 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.2 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.19 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.23 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.23 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.17 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.17 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.18 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.18 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.19 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.3 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.27 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.23 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.21 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.19 |
rpoB | 762032 | c.2226C>T | synonymous_variant | 0.27 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.31 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.31 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.31 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.24 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.23 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.19 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.22 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.29 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.29 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.32 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.19 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.23 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.2 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.2 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.22 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.2 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.16 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.25 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.23 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.37 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.38 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.38 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.38 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.37 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.38 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.4 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.32 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.33 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.29 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.26 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.2 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.16 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.16 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.16 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.24 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.23 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.29 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.29 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.31 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.3 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.28 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.27 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.26 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.25 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.24 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.24 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.21 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.17 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.23 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.23 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.22 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.16 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.19 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.23 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.22 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.23 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.17 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.16 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.17 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.19 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.21 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.26 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.22 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.26 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.26 |
rpoC | 763825 | c.456G>A | synonymous_variant | 0.28 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.27 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.21 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.18 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.17 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.19 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.24 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.33 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.3 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.32 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.32 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.36 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.44 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.33 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.33 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.33 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.26 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.23 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.41 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.45 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.41 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.33 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.34 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.34 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.43 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.54 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.48 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.35 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.4 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.36 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.38 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.31 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.39 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.38 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.37 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.3 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.3 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.27 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.23 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.29 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.26 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.26 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.26 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.3 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.32 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.34 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.37 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.38 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.38 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.37 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.33 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.32 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.32 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.37 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.37 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.39 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.39 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.4 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.35 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.36 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.32 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.28 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.28 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.29 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.27 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.26 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.23 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.27 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.27 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.27 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.23 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.18 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.18 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.22 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.21 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.27 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.21 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.27 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.26 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.34 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.27 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.26 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.27 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.27 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.3 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.3 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.29 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.29 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.3 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.22 |
rpoC | 765292 | c.1923G>C | synonymous_variant | 0.18 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.19 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.19 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.2 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.2 |
rpoC | 765329 | p.Ser654Gly | missense_variant | 0.18 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.19 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.18 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.18 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.25 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.26 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.33 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.45 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.36 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.45 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.47 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.33 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.34 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.32 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.4 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.4 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.41 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.41 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.42 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.41 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.43 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.33 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.29 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.32 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.3 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.33 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.33 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.38 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.38 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.4 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.46 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.57 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.5 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.5 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.5 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.51 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.35 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.38 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.4 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.39 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.36 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.36 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.34 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.31 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.33 |
rpoC | 766083 | p.Ala905Glu | missense_variant | 0.14 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.19 |
rpoC | 766168 | c.2799C>T | synonymous_variant | 0.22 |
rpoC | 766174 | p.Asn935Lys | missense_variant | 0.2 |
rpoC | 766178 | p.Ile937Val | missense_variant | 0.2 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.2 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.2 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.21 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.18 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.22 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.26 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.29 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.24 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.24 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.26 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.19 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.23 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.21 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.18 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.2 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.17 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.17 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.18 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.17 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.18 |
rpoC | 766987 | c.3618G>C | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.2 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.23 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.23 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.25 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.23 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.35 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.32 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.36 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.31 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.29 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.32 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.33 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.33 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.33 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.27 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.25 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.26 |
rpoC | 767265 | p.Ala1299Glu | missense_variant | 0.16 |
rpoC | 767275 | c.3906T>C | synonymous_variant | 0.17 |
rpoC | 767281 | c.3912C>G | synonymous_variant | 0.17 |
rpoC | 767284 | c.3915C>T | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.2 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.19 |
mmpL5 | 776636 | p.Glu615Asp | missense_variant | 0.19 |
mmpL5 | 776646 | p.Val612Thr | missense_variant | 0.17 |
mmpL5 | 776654 | c.1827A>C | synonymous_variant | 0.17 |
mmpL5 | 776664 | p.Thr606Gly | missense_variant | 0.23 |
mmpL5 | 776678 | c.1803G>C | synonymous_variant | 0.21 |
mmpL5 | 776693 | p.Val596Ala | missense_variant | 0.23 |
mmpL5 | 776705 | c.1776C>T | synonymous_variant | 0.26 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781571 | c.12C>T | synonymous_variant | 0.18 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.32 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.31 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.31 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.2 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.19 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.22 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.23 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.25 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.26 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.28 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.24 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.18 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.21 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.22 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.26 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.26 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.27 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.21 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.19 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.16 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.16 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.17 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.17 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.16 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.18 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.17 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.17 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.22 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.23 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.18 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.18 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.16 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.18 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.18 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.19 |
rplC | 801339 | c.531T>C | synonymous_variant | 0.22 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.22 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.23 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.29 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.28 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.22 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.21 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.15 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.19 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 0.81 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.18 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.18 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 0.17 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.17 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.23 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.18 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.19 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.16 |
fbiC | 1303866 | p.Glu312Asp | missense_variant | 0.18 |
fbiC | 1303867 | p.Asp313Asn | missense_variant | 0.18 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.21 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.2 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.22 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.21 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.19 |
fbiC | 1304535 | c.1605G>A | synonymous_variant | 0.28 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.23 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.22 |
fbiC | 1304553 | c.1623C>T | synonymous_variant | 0.32 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.28 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.27 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.28 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.18 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.18 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.21 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.21 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.26 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.29 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.3 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.32 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.31 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.34 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.28 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.26 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.31 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.29 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.31 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.27 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.3 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.3 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.28 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.27 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.27 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.21 |
fbiC | 1305030 | c.2100G>C | synonymous_variant | 0.21 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.21 |
fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.2 |
fbiC | 1305045 | c.2115A>G | synonymous_variant | 0.18 |
atpE | 1460852 | c.-193C>G | upstream_gene_variant | 0.19 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.19 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 0.16 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 0.25 |
atpE | 1460894 | c.-151A>G | upstream_gene_variant | 0.25 |
atpE | 1460897 | c.-148A>C | upstream_gene_variant | 0.21 |
atpE | 1460900 | c.-145T>C | upstream_gene_variant | 0.23 |
atpE | 1460915 | c.-130C>G | upstream_gene_variant | 0.27 |
atpE | 1460918 | c.-127A>G | upstream_gene_variant | 0.26 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.17 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.2 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.17 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.17 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474964 | n.1307T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.2 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.23 |
fabG1 | 1673615 | p.Glu59Val | missense_variant | 0.25 |
fabG1 | 1673637 | p.Asp66Glu | missense_variant | 0.19 |
fabG1 | 1673641 | p.Val68Ile | missense_variant | 0.17 |
inhA | 1673685 | c.-517C>T | upstream_gene_variant | 0.19 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.21 |
fabG1 | 1673716 | p.Ala93Lys | missense_variant | 0.21 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.19 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.17 |
inhA | 1674672 | c.471C>G | synonymous_variant | 0.17 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.25 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.32 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.29 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.27 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.32 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.33 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.2 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.19 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.29 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.29 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.27 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.21 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.24 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.29 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.23 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.26 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.27 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.29 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.26 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.24 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.28 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.29 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.27 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.23 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.22 |
rpsA | 1834081 | c.540C>T | synonymous_variant | 0.26 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.25 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.21 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.22 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.23 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.23 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.22 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.16 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.16 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.18 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.18 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.18 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.18 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.18 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.19 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.17 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.16 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.16 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.16 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.17 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.17 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.21 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.2 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.23 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.27 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.23 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.21 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.32 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.32 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.32 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.23 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.17 |
tlyA | 1917940 | p.Val1Met | missense_variant | 0.15 |
tlyA | 1917943 | p.Ala2Ser | missense_variant | 0.15 |
tlyA | 1917951 | c.12T>C | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917975 | c.36C>G | synonymous_variant | 0.21 |
tlyA | 1917981 | c.42G>C | synonymous_variant | 0.21 |
tlyA | 1917990 | c.51G>C | synonymous_variant | 0.2 |
tlyA | 1917993 | c.54A>G | synonymous_variant | 0.2 |
tlyA | 1917996 | c.57A>G | synonymous_variant | 0.2 |
tlyA | 1918002 | c.63A>G | synonymous_variant | 0.19 |
tlyA | 1918206 | c.267G>C | synonymous_variant | 0.19 |
tlyA | 1918212 | c.273A>G | synonymous_variant | 0.17 |
tlyA | 1918218 | c.279C>G | synonymous_variant | 0.16 |
tlyA | 1918221 | c.282T>C | synonymous_variant | 0.16 |
tlyA | 1918236 | c.297A>C | synonymous_variant | 0.17 |
tlyA | 1918248 | c.309T>C | synonymous_variant | 0.18 |
tlyA | 1918251 | c.312T>G | synonymous_variant | 0.19 |
tlyA | 1918258 | p.His107Glu | missense_variant | 0.18 |
ndh | 2101804 | c.1239T>G | synonymous_variant | 0.26 |
ndh | 2101808 | p.Thr412Ser | missense_variant | 0.24 |
ndh | 2101830 | p.Ile405Val | missense_variant | 0.28 |
ndh | 2101837 | p.Ala402Val | missense_variant | 0.24 |
ndh | 2101912 | c.1131G>C | synonymous_variant | 0.17 |
katG | 2155695 | c.417C>G | synonymous_variant | 0.17 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.16 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169085 | p.Ser510Thr | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.56 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.54 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289930 | c.-689A>G | upstream_gene_variant | 0.18 |
pncA | 2289943 | c.-702T>G | upstream_gene_variant | 0.2 |
pncA | 2289948 | c.-707C>T | upstream_gene_variant | 0.19 |
pncA | 2289949 | c.-708A>G | upstream_gene_variant | 0.2 |
pncA | 2289987 | c.-746C>T | upstream_gene_variant | 0.18 |
pncA | 2289991 | c.-750G>C | upstream_gene_variant | 0.18 |
pncA | 2289994 | c.-753A>G | upstream_gene_variant | 0.18 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.18 |
pncA | 2290009 | c.-768A>G | upstream_gene_variant | 0.23 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.23 |
pncA | 2290024 | c.-783C>G | upstream_gene_variant | 0.17 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.19 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.34 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.28 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.3 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.23 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.21 |
kasA | 2518138 | c.24T>C | synonymous_variant | 0.26 |
kasA | 2518146 | p.Phe11Tyr | missense_variant | 0.2 |
kasA | 2518162 | c.48G>A | synonymous_variant | 0.2 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.22 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.22 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.27 |
kasA | 2518220 | c.106C>T | synonymous_variant | 0.28 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.27 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.26 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.16 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.2 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.25 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.21 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.22 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.23 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.24 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.23 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.24 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.24 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.35 |
kasA | 2518624 | c.510C>G | synonymous_variant | 0.32 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.35 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.25 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.2 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.18 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.18 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.2 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.17 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.17 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.16 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.17 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.19 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.2 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.28 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.25 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.17 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.17 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.17 |
kasA | 2519167 | c.1053T>G | synonymous_variant | 0.21 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.24 |
kasA | 2519196 | p.Thr361Ser | missense_variant | 0.23 |
ahpC | 2726493 | p.Asn101Glu | missense_variant | 0.21 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.15 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.19 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.19 |
folC | 2746426 | c.1173G>C | synonymous_variant | 0.24 |
folC | 2746438 | c.1161G>C | synonymous_variant | 0.24 |
folC | 2746451 | p.Gly383Ala | missense_variant | 0.25 |
folC | 2746478 | p.Phe374Tyr | missense_variant | 0.27 |
folC | 2746480 | c.1119A>C | synonymous_variant | 0.27 |
folC | 2746492 | c.1107G>A | synonymous_variant | 0.25 |
folC | 2746495 | p.His368Gly | missense_variant | 0.25 |
folC | 2746507 | c.1092A>G | synonymous_variant | 0.27 |
folC | 2746510 | c.1089A>G | synonymous_variant | 0.29 |
folC | 2746516 | c.1083T>G | synonymous_variant | 0.33 |
folC | 2746519 | p.Ser360Ala | missense_variant | 0.33 |
folC | 2746525 | c.1074G>T | synonymous_variant | 0.32 |
folC | 2746531 | c.1068G>C | synonymous_variant | 0.29 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.19 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.17 |
folC | 2747335 | c.264G>C | synonymous_variant | 0.19 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.16 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.23 |
Rv2752c | 3064832 | p.Ala454Thr | missense_variant | 0.15 |
Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.16 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.19 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.2 |
Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 0.21 |
Rv2752c | 3065082 | c.1110G>C | synonymous_variant | 0.2 |
Rv2752c | 3065087 | c.1105A>C | synonymous_variant | 0.19 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.17 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.19 |
Rv2752c | 3065115 | c.1077C>A | synonymous_variant | 0.18 |
Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 0.14 |
Rv2752c | 3065412 | c.780G>A | synonymous_variant | 0.21 |
Rv2752c | 3065418 | c.774A>G | synonymous_variant | 0.22 |
Rv2752c | 3065421 | c.771G>A | synonymous_variant | 0.22 |
Rv2752c | 3065442 | c.750T>C | synonymous_variant | 0.23 |
Rv2752c | 3065451 | c.741G>A | synonymous_variant | 0.28 |
Rv2752c | 3065457 | c.735A>C | synonymous_variant | 0.23 |
Rv2752c | 3065463 | c.729T>C | synonymous_variant | 0.23 |
Rv2752c | 3065481 | c.711T>C | synonymous_variant | 0.29 |
Rv2752c | 3065487 | c.705T>G | synonymous_variant | 0.22 |
Rv2752c | 3065490 | c.702A>C | synonymous_variant | 0.22 |
Rv2752c | 3065493 | c.699G>C | synonymous_variant | 0.21 |
Rv2752c | 3065499 | c.693A>C | synonymous_variant | 0.25 |
Rv2752c | 3065502 | p.Asp230Glu | missense_variant | 0.27 |
Rv2752c | 3065508 | c.684T>C | synonymous_variant | 0.25 |
Rv2752c | 3065511 | c.681G>C | synonymous_variant | 0.24 |
Rv2752c | 3065517 | c.675C>G | synonymous_variant | 0.25 |
Rv2752c | 3065523 | c.669C>T | synonymous_variant | 0.22 |
Rv2752c | 3065553 | c.639A>G | synonymous_variant | 0.17 |
Rv2752c | 3066994 | c.-804_-803delCAinsGC | upstream_gene_variant | 0.2 |
Rv2752c | 3066996 | c.-805T>C | upstream_gene_variant | 0.2 |
Rv2752c | 3067001 | c.-810G>A | upstream_gene_variant | 0.18 |
Rv2752c | 3067017 | c.-827_-826delGGinsAC | upstream_gene_variant | 0.16 |
Rv2752c | 3067020 | c.-829G>C | upstream_gene_variant | 0.16 |
Rv2752c | 3067038 | c.-847G>T | upstream_gene_variant | 0.15 |
Rv2752c | 3067047 | c.-856T>C | upstream_gene_variant | 0.16 |
Rv2752c | 3067052 | c.-861G>C | upstream_gene_variant | 0.16 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.16 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.35 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.25 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.25 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.33 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.19 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.19 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.22 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.22 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.19 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.25 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.21 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.2 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.16 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.29 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.29 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.35 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.37 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.41 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.44 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.4 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.41 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.35 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.32 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.26 |
thyX | 3067583 | c.363C>G | synonymous_variant | 0.31 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.29 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.23 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.23 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.21 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.21 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.21 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.23 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.29 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.29 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.3 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.21 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.22 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.21 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.18 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.21 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.16 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.2 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.2 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.27 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.2 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.21 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.22 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.2 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.22 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.19 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.19 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.17 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.2 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.18 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.19 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.18 |
thyA | 3074028 | c.444G>C | synonymous_variant | 0.22 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.22 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.22 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.22 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.22 |
thyA | 3074055 | p.Glu139Pro | missense_variant | 0.19 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.19 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.18 |
thyA | 3074102 | p.Asp124Asn | missense_variant | 0.17 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.17 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.22 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.23 |
thyA | 3074175 | c.297A>G | synonymous_variant | 0.21 |
thyA | 3074181 | c.291A>G | synonymous_variant | 0.19 |
thyA | 3074187 | c.285T>C | synonymous_variant | 0.2 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.2 |
thyA | 3074214 | c.258T>C | synonymous_variant | 0.19 |
ald | 3087272 | c.453A>C | synonymous_variant | 0.2 |
ald | 3087278 | p.Gln153His | missense_variant | 0.2 |
ald | 3087281 | c.462G>C | synonymous_variant | 0.2 |
ald | 3087284 | c.465C>G | synonymous_variant | 0.21 |
ald | 3087290 | c.471T>C | synonymous_variant | 0.21 |
ald | 3087305 | c.486G>C | synonymous_variant | 0.24 |
ald | 3087311 | c.492C>G | synonymous_variant | 0.22 |
ald | 3087318 | p.Glu167Lys | missense_variant | 0.21 |
ald | 3087635 | c.816C>T | synonymous_variant | 0.14 |
fbiB | 3641950 | p.Arg139Leu | missense_variant | 0.14 |
fbiB | 3642701 | c.1167C>G | synonymous_variant | 0.22 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.25 |
fbiB | 3642731 | c.1197C>G | synonymous_variant | 0.25 |
fbiB | 3642743 | c.1209T>C | synonymous_variant | 0.23 |
fbiB | 3642758 | c.1224C>G | synonymous_variant | 0.15 |
alr | 3841001 | c.420A>G | synonymous_variant | 0.16 |
alr | 3841010 | c.411A>G | synonymous_variant | 0.17 |
alr | 3841017 | p.Leu135Gln | missense_variant | 0.17 |
alr | 3841022 | c.399C>G | synonymous_variant | 0.17 |
alr | 3841028 | c.393G>C | synonymous_variant | 0.19 |
alr | 3841033 | p.Val130Ile | missense_variant | 0.18 |
alr | 3841037 | c.384G>C | synonymous_variant | 0.18 |
alr | 3841069 | p.Ile118Phe | missense_variant | 0.18 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.16 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.2 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.21 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.32 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.31 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.28 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.32 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.35 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.3 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.3 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.29 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.25 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.19 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.21 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.24 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.22 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.22 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.19 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.22 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.29 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.31 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.26 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.24 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.3 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.24 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.24 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.26 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.23 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.21 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.19 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.23 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.23 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.23 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.21 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.22 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.24 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.25 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.25 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.28 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.23 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.22 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.19 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.17 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.17 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.17 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.16 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878115 | c.393G>A | synonymous_variant | 0.16 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.16 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.17 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.19 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.17 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.18 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.19 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.2 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.19 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.15 |
rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 0.25 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.27 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.19 |
clpC1 | 4038177 | p.Pro843Leu | missense_variant | 0.13 |
clpC1 | 4038239 | c.2466T>C | synonymous_variant | 0.17 |
clpC1 | 4038255 | p.Val817Lys | missense_variant | 0.19 |
clpC1 | 4038272 | c.2433T>C | synonymous_variant | 0.16 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.33 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.21 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.19 |
clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.17 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.17 |
clpC1 | 4038320 | c.2385G>C | synonymous_variant | 0.21 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.24 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.24 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.21 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.19 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.19 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.15 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.18 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.16 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.19 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.19 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.21 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 0.19 |
clpC1 | 4038497 | p.Ser736Gln | missense_variant | 0.18 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.28 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.18 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.24 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.28 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.27 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.26 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.28 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.3 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.32 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.39 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.37 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.39 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.37 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.39 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.23 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.23 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.25 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.26 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.26 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.22 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.26 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.27 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.28 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.28 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.3 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.28 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.31 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.34 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.31 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.32 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.34 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.39 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.4 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.36 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.37 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.38 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.37 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.39 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.39 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.25 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.26 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.21 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.21 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.2 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.22 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.19 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.3 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.34 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.39 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.34 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.33 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.33 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.29 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.29 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.29 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.3 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.32 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.28 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.19 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.22 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.22 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.22 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.21 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.17 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.18 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 0.24 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.24 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.3 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.2 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.2 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.21 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.21 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.21 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.21 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.21 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.2 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.26 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.24 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.26 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.17 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.17 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.21 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.23 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.29 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.3 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.26 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.27 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.27 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.26 |
clpC1 | 4040090 | p.Ser205Thr | missense_variant | 0.15 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.16 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.2 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.23 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.19 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.18 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.24 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.16 |
clpC1 | 4040278 | p.Ser143Thr | missense_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.3 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.33 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.31 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.21 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.15 |
panD | 4044072 | c.210C>G | synonymous_variant | 0.18 |
panD | 4044075 | c.207T>C | synonymous_variant | 0.18 |
panD | 4044165 | c.117G>C | synonymous_variant | 0.17 |
embC | 4240267 | c.405T>C | synonymous_variant | 0.17 |
embC | 4240270 | c.408T>C | synonymous_variant | 0.17 |
embC | 4240277 | p.Leu139Val | missense_variant | 0.19 |
embC | 4240282 | c.420C>G | synonymous_variant | 0.2 |
embC | 4240284 | p.Thr141Ser | missense_variant | 0.2 |
embC | 4240288 | c.426C>G | synonymous_variant | 0.21 |
embC | 4240297 | c.435T>C | synonymous_variant | 0.27 |
embC | 4240313 | p.Thr151Ala | missense_variant | 0.27 |
embC | 4240318 | c.456T>C | synonymous_variant | 0.3 |
embC | 4240654 | c.792C>G | synonymous_variant | 0.16 |
embC | 4240660 | c.798C>G | synonymous_variant | 0.16 |
embC | 4240669 | c.807G>C | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.18 |
embC | 4240677 | p.Gly272Ala | missense_variant | 0.17 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.17 |
embC | 4240693 | c.831T>G | synonymous_variant | 0.15 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.18 |
embC | 4241002 | c.1140G>C | synonymous_variant | 0.23 |
embC | 4241013 | p.Met384Thr | missense_variant | 0.25 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.21 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.21 |
embC | 4241032 | c.1170G>C | synonymous_variant | 0.24 |
embC | 4241038 | c.1176G>C | synonymous_variant | 0.23 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.22 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.23 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.21 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.22 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.22 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.27 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.19 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.21 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.21 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.17 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.17 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.17 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.18 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.18 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.19 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.2 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242820 | c.-413G>C | upstream_gene_variant | 0.23 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.23 |
embA | 4242841 | c.-392C>T | upstream_gene_variant | 0.15 |
embA | 4242847 | c.-386C>A | upstream_gene_variant | 0.15 |
embA | 4242859 | c.-374C>T | upstream_gene_variant | 0.16 |
embC | 4242863 | p.Tyr1001Asn | missense_variant | 0.2 |
embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.23 |
embA | 4242892 | c.-341G>C | upstream_gene_variant | 0.24 |
embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.19 |
embA | 4244207 | c.975C>G | synonymous_variant | 0.27 |
embA | 4244219 | c.987C>G | synonymous_variant | 0.15 |
embA | 4244534 | c.1302T>C | synonymous_variant | 0.18 |
embA | 4244537 | c.1305T>G | synonymous_variant | 0.18 |
embA | 4244543 | c.1311C>G | synonymous_variant | 0.18 |
embA | 4244547 | p.Ile439Val | missense_variant | 0.17 |
embA | 4244619 | c.1387T>C | synonymous_variant | 0.16 |
embA | 4244631 | p.Thr467Leu | missense_variant | 0.17 |
embA | 4244880 | p.Trp550Arg | missense_variant | 0.2 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.17 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.24 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.25 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.26 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.22 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.18 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.22 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.24 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.23 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.27 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.24 |
embA | 4245248 | c.2016G>C | synonymous_variant | 0.18 |
embA | 4245257 | c.2025A>G | synonymous_variant | 0.21 |
embA | 4245263 | c.2031A>G | synonymous_variant | 0.21 |
embA | 4245282 | p.Ile684Val | missense_variant | 0.19 |
embA | 4245285 | c.2053T>C | synonymous_variant | 0.19 |
embA | 4245290 | c.2058C>G | synonymous_variant | 0.16 |
embA | 4245299 | c.2067A>G | synonymous_variant | 0.19 |
embA | 4245315 | p.Val695Met | missense_variant | 0.19 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.18 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.16 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.17 |
embA | 4245772 | p.Asn847Thr | missense_variant | 0.17 |
embB | 4245785 | c.-729G>C | upstream_gene_variant | 0.17 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.2 |
embB | 4245812 | c.-702G>C | upstream_gene_variant | 0.23 |
embA | 4245813 | p.Pro861Ala | missense_variant | 0.23 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.21 |
embB | 4245824 | c.-690G>C | upstream_gene_variant | 0.24 |
embB | 4245833 | c.-681G>C | upstream_gene_variant | 0.29 |
embB | 4245842 | c.-672G>C | upstream_gene_variant | 0.29 |
embB | 4245845 | c.-669T>C | upstream_gene_variant | 0.29 |
embB | 4245851 | c.-663G>C | upstream_gene_variant | 0.29 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.26 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.29 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.86 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.86 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.86 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.5 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.5 |
embB | 4247434 | c.921C>G | synonymous_variant | 0.17 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.17 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4247446 | c.933C>T | synonymous_variant | 0.16 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.21 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.22 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.19 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.21 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.21 |
embB | 4247566 | c.1053C>A | synonymous_variant | 0.14 |
embB | 4247629 | c.1116C>G | synonymous_variant | 0.2 |
embB | 4247632 | c.1119C>G | synonymous_variant | 0.21 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.22 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.29 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.27 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.27 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.28 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.28 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.3 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.32 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.35 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.27 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.38 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.38 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.38 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.44 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.42 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.26 |
embB | 4248040 | c.1527C>G | synonymous_variant | 0.26 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.26 |
embB | 4248044 | p.Lys511Ala | missense_variant | 0.26 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.26 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.29 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.3 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.28 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.28 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.28 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.28 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.28 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.22 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.16 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.19 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.19 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.18 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.18 |
embB | 4248361 | c.1848A>C | synonymous_variant | 0.17 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.17 |
embB | 4248373 | c.1860C>G | synonymous_variant | 0.17 |
aftB | 4267256 | c.1581C>G | synonymous_variant | 0.19 |
aftB | 4267262 | c.1575T>C | synonymous_variant | 0.2 |
aftB | 4267266 | p.Ala524Gly | missense_variant | 0.19 |
aftB | 4267268 | c.1569T>C | synonymous_variant | 0.19 |
ubiA | 4269077 | p.Ile253Val | missense_variant | 0.14 |
aftB | 4269084 | c.-248G>C | upstream_gene_variant | 0.16 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.17 |
aftB | 4269131 | c.-295C>T | upstream_gene_variant | 0.15 |
aftB | 4269132 | c.-296G>C | upstream_gene_variant | 0.15 |
aftB | 4269138 | c.-302C>T | upstream_gene_variant | 0.14 |
aftB | 4269179 | c.-343C>A | upstream_gene_variant | 0.17 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.16 |
aftB | 4269186 | c.-350C>G | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |