Run ID: ERR6866125
Sample name:
Date: 02-04-2023 03:16:16
Number of reads: 493774
Percentage reads mapped: 28.09
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6269 | p.Asn344Glu | missense_variant | 0.15 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.21 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.21 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.21 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.2 |
gyrB | 6301 | c.1062G>C | synonymous_variant | 0.21 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.2 |
gyrB | 6308 | p.Val357Ile | missense_variant | 0.2 |
gyrA | 6316 | c.-986G>C | upstream_gene_variant | 0.2 |
gyrB | 6326 | p.Ser363Ala | missense_variant | 0.19 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.2 |
gyrA | 6362 | c.-940_-938delTTGinsCTC | upstream_gene_variant | 0.19 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.18 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.18 |
gyrB | 6399 | p.Val387Ala | missense_variant | 0.2 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.14 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.25 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.5 |
gyrB | 6663 | p.Phe475Tyr | missense_variant | 0.46 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.5 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.46 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.59 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.61 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.61 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.61 |
gyrA | 6724 | c.-578G>C | upstream_gene_variant | 0.61 |
gyrA | 6727 | c.-575G>C | upstream_gene_variant | 0.61 |
gyrA | 6730 | c.-572A>C | upstream_gene_variant | 0.61 |
gyrB | 6737 | p.Thr500Ala | missense_variant | 0.58 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.55 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.52 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.5 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.48 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 0.48 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.48 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.48 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 0.47 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.33 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.22 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491386 | p.Leu202Ile | missense_variant | 0.25 |
fgd1 | 491590 | p.Lys270Val | missense_variant | 0.23 |
fgd1 | 491604 | c.822G>C | synonymous_variant | 0.23 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.27 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.27 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.25 |
fgd1 | 491631 | c.849C>G | synonymous_variant | 0.25 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.24 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.24 |
rpoB | 760112 | c.306T>G | synonymous_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.71 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.29 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.27 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.27 |
rpoB | 760133 | c.327C>G | synonymous_variant | 0.27 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.24 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.24 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.32 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.35 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.32 |
rpoB | 760185 | c.379C>T | synonymous_variant | 0.32 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.3 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.21 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.2 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.31 |
rpoB | 760283 | c.477G>A | synonymous_variant | 0.33 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.44 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.43 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.43 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.43 |
rpoB | 760317 | c.511_513delAGCinsTCG | synonymous_variant | 0.43 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.45 |
rpoB | 760331 | c.525G>T | synonymous_variant | 0.45 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.44 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.46 |
rpoB | 760356 | p.Thr184Ser | missense_variant | 0.54 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.52 |
rpoB | 760368 | c.562_563delTCinsAG | synonymous_variant | 0.56 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.6 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.65 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.67 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.6 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.6 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.5 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.32 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.3 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.23 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.23 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.19 |
rpoB | 760880 | c.1074G>C | synonymous_variant | 0.18 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.2 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.2 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.2 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.39 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.39 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.37 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.4 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.45 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.46 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.52 |
rpoB | 760961 | c.1155C>G | synonymous_variant | 0.52 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.52 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.52 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.54 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.62 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.62 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.69 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.68 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.62 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.62 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.64 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.66 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.62 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.62 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.63 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.63 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.59 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.58 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.58 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.61 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.57 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.57 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.59 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.65 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.62 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.62 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.63 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.65 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.66 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.69 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.67 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.65 |
rpoB | 761255 | c.1449T>C | synonymous_variant | 0.64 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.61 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.62 |
rpoB | 761274 | c.1468C>T | synonymous_variant | 0.59 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.58 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 0.59 |
rpoB | 761300 | c.1494G>A | synonymous_variant | 0.48 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 0.36 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.33 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.32 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.27 |
rpoB | 761347 | p.Val514Glu | missense_variant | 0.27 |
rpoB | 761349 | p.Asp515Asn | missense_variant | 0.27 |
rpoB | 761355 | p.Val517Gln | missense_variant | 0.29 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.27 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.27 |
rpoB | 761367 | p.Glu521Gln | missense_variant | 0.26 |
rpoB | 761370 | p.Ile522Val | missense_variant | 0.27 |
rpoB | 761374 | p.Val523Asp | missense_variant | 0.25 |
rpoB | 761387 | c.1581C>G | synonymous_variant | 0.26 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.26 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.24 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.35 |
rpoB | 761540 | c.1734C>T | synonymous_variant | 0.33 |
rpoB | 761549 | c.1743G>C | synonymous_variant | 0.4 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.48 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.48 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.45 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.45 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.44 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.44 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.43 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.43 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.43 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.43 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.43 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.37 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.33 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.32 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.21 |
rpoB | 761694 | p.Ile630Val | missense_variant | 0.2 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 0.23 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.36 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.43 |
rpoB | 761996 | c.2190C>T | synonymous_variant | 0.67 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.64 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.64 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.64 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.67 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.67 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.67 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.71 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.72 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.72 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.77 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.75 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.68 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.71 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.67 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.66 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.66 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.68 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.68 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.61 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 0.66 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.62 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.59 |
rpoB | 762189 | p.Ile795Val | missense_variant | 0.64 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.62 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.59 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.56 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.5 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.49 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.47 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.45 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.43 |
rpoB | 762299 | c.2493G>C | synonymous_variant | 0.43 |
rpoB | 762308 | c.2502G>C | synonymous_variant | 0.46 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.44 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.42 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.37 |
rpoB | 762335 | c.2529C>T | synonymous_variant | 0.35 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.21 |
rpoC | 762800 | c.-570C>G | upstream_gene_variant | 0.14 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.33 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.32 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.32 |
rpoC | 762827 | c.-543G>T | upstream_gene_variant | 0.35 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.35 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.61 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.61 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.58 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.68 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.75 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.79 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.79 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.8 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.79 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.76 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.73 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.75 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.74 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.68 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.63 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.61 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.61 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.62 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.57 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.59 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.62 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.62 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.62 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.63 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.52 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.39 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.37 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.28 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.26 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 0.28 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.13 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.33 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.33 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.37 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.38 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.5 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.59 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.63 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.7 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.71 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.77 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.76 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.75 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.73 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.76 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.77 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.74 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.74 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.74 |
rpoC | 763624 | c.255C>G | synonymous_variant | 0.58 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.5 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.43 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.45 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.42 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.32 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.32 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.33 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.32 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.32 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.3 |
rpoC | 763732 | c.363C>T | synonymous_variant | 0.3 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.29 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.3 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.22 |
rpoC | 763776 | c.409_410delAC | frameshift_variant | 0.19 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.19 |
rpoC | 763783 | c.415_416dupGT | frameshift_variant | 0.19 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.26 |
rpoC | 763801 | c.432C>T | synonymous_variant | 0.26 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.26 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.17 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.15 |
rpoC | 764002 | c.633C>T | synonymous_variant | 0.14 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.14 |
rpoC | 764020 | c.651C>T | synonymous_variant | 0.15 |
rpoC | 764023 | c.654G>T | synonymous_variant | 0.15 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.15 |
rpoC | 764029 | p.Glu220Asp | missense_variant | 0.17 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.17 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.15 |
rpoC | 764044 | c.675T>G | synonymous_variant | 0.15 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.15 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.25 |
rpoC | 764149 | c.780G>C | synonymous_variant | 0.18 |
rpoC | 764157 | p.Lys263Ile | missense_variant | 0.18 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.19 |
rpoC | 764164 | p.Ile265Met | missense_variant | 0.2 |
rpoC | 764165 | p.Glu266Arg | missense_variant | 0.2 |
rpoC | 764182 | p.Asp271Glu | missense_variant | 0.3 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.3 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.37 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.39 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.39 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.44 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.42 |
rpoC | 764227 | c.858G>T | synonymous_variant | 0.45 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.54 |
rpoC | 764242 | c.873C>T | synonymous_variant | 0.5 |
rpoC | 764245 | c.876C>G | synonymous_variant | 0.5 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.57 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.57 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.54 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.58 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.62 |
rpoC | 764296 | c.927G>C | synonymous_variant | 0.66 |
rpoC | 764308 | c.939G>T | synonymous_variant | 0.66 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.61 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.67 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.66 |
rpoC | 764368 | c.999C>T | synonymous_variant | 0.68 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.67 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.66 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.63 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.56 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.58 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.58 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.56 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.54 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.54 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.54 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.56 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.58 |
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 | 0.65 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.65 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.57 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.6 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.6 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.6 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.67 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.7 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.64 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.65 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.78 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.79 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.78 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.79 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.72 |
rpoC | 764707 | c.1338G>C | synonymous_variant | 0.71 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.7 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.7 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.61 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.58 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.53 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.54 |
rpoC | 764785 | c.1416C>G | synonymous_variant | 0.56 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.5 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.48 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.48 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.45 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.39 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.38 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.39 |
rpoC | 764843 | p.Ala492Asn | missense_variant | 0.35 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.39 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.38 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.43 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.38 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.29 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.29 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.27 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.15 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.26 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.33 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.32 |
rpoC | 764995 | c.1626C>A | synonymous_variant | 0.35 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.33 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.35 |
rpoC | 765011 | c.1642_1644delAGCinsTCG | synonymous_variant | 0.35 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.37 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.37 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.35 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.33 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.33 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.33 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.33 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.32 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.2 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.2 |
rpoC | 765082 | c.1713G>T | synonymous_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.26 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.26 |
rpoC | 765883 | c.2514C>T | synonymous_variant | 0.28 |
rpoC | 765890 | p.Arg841Lys | missense_variant | 0.25 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.27 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 0.29 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.31 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.25 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.25 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.24 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.24 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.24 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.24 |
rpoC | 765955 | c.2586C>T | synonymous_variant | 0.25 |
rpoC | 765961 | c.2592G>T | synonymous_variant | 0.24 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.24 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.25 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.25 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.25 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.21 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.3 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.3 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.3 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.3 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.33 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 0.3 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.27 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.27 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.27 |
rpoC | 766402 | c.3033C>G | synonymous_variant | 0.21 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.19 |
rpoC | 766425 | c.3056_3057insTGCGGC | disruptive_inframe_insertion | 0.2 |
rpoC | 766428 | p.Val1020Gly | missense_variant | 0.2 |
rpoC | 766431 | p.Gly1021Ala | missense_variant | 0.18 |
rpoC | 766434 | p.Glu1022Ala | missense_variant | 0.18 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.18 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.18 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.18 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.2 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.2 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.2 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.19 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 0.2 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.21 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 0.2 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.19 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.19 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.18 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.25 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.28 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.33 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.33 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.33 |
rpoC | 766910 | p.Ile1181Val | missense_variant | 0.3 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.32 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.32 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766934 | p.Glu1189Ser | missense_variant | 0.18 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.17 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.17 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.17 |
rpoC | 766951 | c.3582G>C | synonymous_variant | 0.19 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.18 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.18 |
rpoC | 766969 | c.3600C>T | synonymous_variant | 0.24 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.33 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.43 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.53 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.63 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.62 |
rpoC | 767093 | c.3724_3726delAGCinsTCG | synonymous_variant | 0.56 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.56 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.56 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.58 |
rpoC | 767113 | c.3744G>C | synonymous_variant | 0.62 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.6 |
rpoC | 767152 | c.3783T>C | synonymous_variant | 0.59 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.59 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.53 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.5 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.47 |
rpoC | 767185 | c.3816G>T | synonymous_variant | 0.47 |
rpoC | 767203 | c.3834C>T | synonymous_variant | 0.36 |
rpoC | 767209 | c.3840T>G | synonymous_variant | 0.33 |
rpoC | 767212 | c.3843G>T | synonymous_variant | 0.31 |
rpoC | 767219 | p.Thr1284Ala | missense_variant | 0.31 |
rpoC | 767222 | p.Ile1285Val | missense_variant | 0.29 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.33 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.33 |
rpoC | 767236 | p.Glu1289Asp | missense_variant | 0.33 |
rpoC | 767239 | c.3870T>C | synonymous_variant | 0.33 |
rpoC | 767256 | c.3887_3888insGGG | disruptive_inframe_insertion | 0.25 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.25 |
rpoC | 767264 | p.Ala1299Thr | missense_variant | 0.25 |
rpoC | 767268 | p.Ala1300Gly | missense_variant | 0.25 |
rpoC | 767281 | c.3912C>G | synonymous_variant | 0.25 |
rpoC | 767284 | c.3915C>T | synonymous_variant | 0.25 |
rpoC | 767304 | p.Tyr1312Phe | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781559 | c.-1G>C | upstream_gene_variant | 0.33 |
rpsL | 781572 | p.Gln5Asn | missense_variant | 0.29 |
rpsL | 781592 | c.33T>C | synonymous_variant | 0.29 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.29 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.29 |
rpsL | 781605 | p.Ile16Ala | missense_variant | 0.28 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.28 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.35 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.44 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.44 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.47 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.56 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.5 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.36 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.36 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.4 |
rpsL | 781725 | p.Lys56Arg | missense_variant | 0.4 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.4 |
rpsL | 781732 | c.174_177delGAGT | frameshift_variant | 0.4 |
rpsL | 781739 | c.180_181insCTCT | frameshift_variant | 0.33 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.36 |
rpsL | 781754 | c.195G>T | synonymous_variant | 0.31 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.33 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.31 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.31 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.5 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.48 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.45 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.45 |
rpsL | 781829 | c.270G>T | synonymous_variant | 0.43 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.43 |
rpsL | 781856 | c.297C>T | synonymous_variant | 0.5 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.5 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.46 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.46 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.45 |
rpsL | 781898 | c.339A>G | synonymous_variant | 0.47 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.44 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.44 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.44 |
rplC | 800610 | c.-199_-197delCTAinsTTG | upstream_gene_variant | 0.18 |
rplC | 800615 | c.-194G>T | upstream_gene_variant | 0.22 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.22 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.3 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.26 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.22 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.24 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.28 |
rplC | 800693 | c.-116A>T | upstream_gene_variant | 0.26 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.28 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.25 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.26 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.29 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.29 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.32 |
rplC | 800780 | c.-29C>G | upstream_gene_variant | 0.25 |
fbiC | 1303515 | c.585G>C | synonymous_variant | 0.2 |
fbiC | 1303525 | p.Ser199Glu | missense_variant | 0.18 |
fbiC | 1303533 | p.Met201Ile | missense_variant | 0.18 |
fbiC | 1303539 | c.609G>A | synonymous_variant | 0.18 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.18 |
fbiC | 1303926 | c.996G>A | synonymous_variant | 0.14 |
fbiC | 1303927 | p.Ala333Ser | missense_variant | 0.14 |
fbiC | 1303932 | c.1002G>A | synonymous_variant | 0.14 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.16 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.18 |
fbiC | 1303974 | c.1044C>T | synonymous_variant | 0.17 |
fbiC | 1303977 | c.1047C>G | synonymous_variant | 0.17 |
fbiC | 1303980 | c.1050G>C | synonymous_variant | 0.17 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.16 |
fbiC | 1304019 | c.1089C>T | synonymous_variant | 0.18 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.18 |
fbiC | 1304028 | c.1098C>T | synonymous_variant | 0.18 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.14 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.29 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.28 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.24 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.25 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.25 |
fbiC | 1304649 | c.1719C>T | synonymous_variant | 0.24 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.22 |
fbiC | 1304660 | p.Tyr577Phe | missense_variant | 0.22 |
fbiC | 1304662 | p.Ser578Thr | missense_variant | 0.22 |
fbiC | 1304670 | c.1740G>C | synonymous_variant | 0.23 |
fbiC | 1304671 | c.1742delT | frameshift_variant | 0.24 |
fbiC | 1304676 | c.1747dupG | frameshift_variant | 0.24 |
fbiC | 1304682 | c.1752C>G | synonymous_variant | 0.24 |
fbiC | 1304694 | c.1764A>G | synonymous_variant | 0.25 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.26 |
fbiC | 1304712 | c.1782C>G | synonymous_variant | 0.26 |
fbiC | 1304715 | c.1785G>A | synonymous_variant | 0.28 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.27 |
fbiC | 1304727 | c.1797A>C | synonymous_variant | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472312 | n.467_468insA | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472463 | n.618G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472858 | n.1013G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472861 | n.1016G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472862 | n.1017T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472863 | n.1018T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473791 | n.134A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473792 | n.135C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473803 | n.146G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473804 | n.147T>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474220 | n.563G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474292 | n.636_642delTCCTCTC | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474303 | n.646A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474305 | n.648G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474309 | n.653delT | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474411 | n.756_778delACCCACACGCGCATACGCGCGTG | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474437 | n.780G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474438 | n.781A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474439 | n.782A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474638 | n.981C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474711 | n.1054G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475414 | n.1757G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475761 | n.2104C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475766 | n.2109G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476689 | n.3032A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476692 | n.3035T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476694 | n.3037G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476695 | n.3038T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476699 | n.3042A>G | non_coding_transcript_exon_variant | 0.43 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.23 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.21 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.21 |
rpsA | 1833607 | c.66T>C | synonymous_variant | 0.2 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.19 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.19 |
rpsA | 1833623 | p.Lys28Ala | missense_variant | 0.18 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.39 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.39 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.39 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.41 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.39 |
rpsA | 1833697 | c.156C>T | synonymous_variant | 0.41 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.37 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.29 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.21 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.21 |
rpsA | 1833739 | c.198C>T | synonymous_variant | 0.23 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.21 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.5 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.52 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.52 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.57 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.56 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.56 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.56 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.56 |
rpsA | 1833838 | c.297G>A | synonymous_variant | 0.56 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.58 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.58 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.58 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.54 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.52 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.51 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.54 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.53 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.48 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.48 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.48 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.48 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.47 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.5 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.48 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.53 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.52 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.5 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.52 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.48 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.44 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.42 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.33 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.36 |
rpsA | 1834108 | c.567C>A | synonymous_variant | 0.32 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.36 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.35 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.25 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.25 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.25 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.28 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.29 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 0.29 |
rpsA | 1834172 | c.631_632insGG | frameshift_variant | 0.28 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.28 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.29 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.4 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.32 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.32 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.3 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.24 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.27 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.23 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.23 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.36 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.38 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.4 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.4 |
rpsA | 1834307 | p.Asp256Asn | missense_variant | 0.4 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.52 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.53 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.49 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.45 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.47 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.48 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.47 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.47 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.47 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.53 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.56 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.56 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.58 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.62 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.63 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.65 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.57 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.55 |
rpsA | 1834474 | c.933C>T | synonymous_variant | 0.48 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.5 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.53 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.47 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.41 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.44 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.44 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.44 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.44 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.44 |
rpsA | 1834570 | c.1029C>T | synonymous_variant | 0.47 |
rpsA | 1834574 | p.Met345Leu | missense_variant | 0.47 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.48 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.48 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.5 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.55 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.52 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.48 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.44 |
rpsA | 1834650 | p.Thr370Asn | missense_variant | 0.4 |
rpsA | 1834653 | p.Glu371Ala | missense_variant | 0.4 |
rpsA | 1834663 | c.1122C>T | synonymous_variant | 0.38 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.39 |
rpsA | 1834688 | c.1147_1149delAGTinsTCG | synonymous_variant | 0.41 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.35 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.33 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.33 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.3 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.29 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.29 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.2 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.23 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.24 |
rpsA | 1834787 | p.Ala416Ser | missense_variant | 0.24 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.21 |
rpsA | 1834804 | c.1263C>T | synonymous_variant | 0.25 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.25 |
rpsA | 1834813 | c.1272G>C | synonymous_variant | 0.25 |
rpsA | 1834831 | c.1290G>T | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.27 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.26 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.25 |
kasA | 2517959 | c.-156C>T | upstream_gene_variant | 0.26 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.26 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.26 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.25 |
kasA | 2517983 | c.-132T>C | upstream_gene_variant | 0.22 |
kasA | 2517986 | c.-129C>T | upstream_gene_variant | 0.18 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.18 |
kasA | 2518008 | c.-107C>G | upstream_gene_variant | 0.18 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.23 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.43 |
thyA | 3073874 | p.Ile200Val | missense_variant | 0.5 |
thyA | 3073878 | p.Glu198Asp | missense_variant | 0.5 |
thyA | 3073884 | c.588C>G | synonymous_variant | 0.46 |
thyA | 3073888 | p.Ser195Glu | missense_variant | 0.46 |
thyA | 3073890 | c.580_582delTTGinsCTC | synonymous_variant | 0.43 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.43 |
thyA | 3073902 | p.Ala190Gln | missense_variant | 0.4 |
thyA | 3073905 | c.567C>G | synonymous_variant | 0.38 |
thyA | 3073910 | p.Met188Val | missense_variant | 0.38 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.38 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.39 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.39 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.38 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.36 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.21 |
rpoA | 3877638 | c.870T>A | synonymous_variant | 0.27 |
rpoA | 3877644 | c.864C>T | synonymous_variant | 0.29 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.33 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.33 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.33 |
rpoA | 3877677 | p.Ala277Gly | missense_variant | 0.36 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.33 |
rpoA | 3877685 | c.823C>T | synonymous_variant | 0.33 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.33 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.33 |
rpoA | 3877701 | c.807G>T | synonymous_variant | 0.38 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.36 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.36 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.36 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.3 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.3 |
rpoA | 3878219 | p.Leu97Val | missense_variant | 0.25 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.2 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.27 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.38 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.43 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.4 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.4 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.4 |
rpoA | 3878304 | c.204G>T | synonymous_variant | 0.5 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.46 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.46 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.46 |
rpoA | 3878331 | c.177A>C | synonymous_variant | 0.46 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.46 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.5 |
rpoA | 3878343 | c.165C>T | synonymous_variant | 0.5 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.46 |
rpoA | 3878358 | c.150C>T | synonymous_variant | 0.46 |
rpoA | 3878361 | c.147G>T | synonymous_variant | 0.46 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.46 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.36 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.38 |
rpoA | 3878406 | c.102G>C | synonymous_variant | 0.42 |
rpoA | 3878415 | c.93C>G | synonymous_variant | 0.27 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.17 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.17 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.17 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.17 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.23 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.42 |
clpC1 | 4038746 | c.1959C>T | synonymous_variant | 0.43 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.4 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.4 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.47 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.47 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.53 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.53 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.52 |
clpC1 | 4038815 | c.1890G>A | synonymous_variant | 0.54 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.52 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.53 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.53 |
clpC1 | 4038881 | c.1824C>T | synonymous_variant | 0.57 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.61 |
clpC1 | 4038905 | c.1800A>T | synonymous_variant | 0.62 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.62 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.62 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.62 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.64 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.65 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.62 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.63 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.7 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.7 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.71 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.71 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.67 |
clpC1 | 4039007 | c.1698G>C | synonymous_variant | 0.66 |
clpC1 | 4039010 | c.1695G>A | synonymous_variant | 0.68 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.66 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.47 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.47 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.44 |
clpC1 | 4039082 | c.1623C>T | synonymous_variant | 0.44 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.47 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.47 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.48 |
clpC1 | 4039100 | c.1605C>G | synonymous_variant | 0.48 |
clpC1 | 4039106 | c.1599G>T | synonymous_variant | 0.49 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.45 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.47 |
clpC1 | 4039133 | c.1572C>T | synonymous_variant | 0.46 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.44 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.43 |
clpC1 | 4039169 | c.1536A>G | synonymous_variant | 0.43 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.45 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.43 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.37 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.4 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.38 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.5 |
clpC1 | 4039217 | c.1488G>C | synonymous_variant | 0.5 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.45 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.45 |
clpC1 | 4039279 | p.Val476Ile | missense_variant | 0.43 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.43 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.43 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.43 |
clpC1 | 4039295 | c.1410A>G | synonymous_variant | 0.46 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.43 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.43 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.46 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.46 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.44 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.44 |
clpC1 | 4039337 | c.1368A>C | synonymous_variant | 0.44 |
clpC1 | 4039347 | p.Arg453Lys | missense_variant | 0.43 |
clpC1 | 4039355 | c.1350G>C | synonymous_variant | 0.38 |
clpC1 | 4039359 | p.Ser449Asn | missense_variant | 0.38 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.36 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.45 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.36 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.33 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.33 |
clpC1 | 4039406 | c.1299G>C | synonymous_variant | 0.29 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.27 |
clpC1 | 4039412 | c.1293T>C | synonymous_variant | 0.29 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.32 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 0.27 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.27 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.24 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.24 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.25 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.26 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.21 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.24 |
clpC1 | 4039478 | c.1227G>A | synonymous_variant | 0.25 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.25 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.25 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.24 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.33 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.35 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.25 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.25 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.27 |
clpC1 | 4039553 | c.1152C>T | synonymous_variant | 0.22 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.22 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.22 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.25 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.25 |
clpC1 | 4039568 | p.Met379Leu | missense_variant | 0.29 |
clpC1 | 4039574 | p.Ala377Ser | missense_variant | 0.29 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.29 |
clpC1 | 4039580 | c.1125C>G | synonymous_variant | 0.29 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.22 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.4 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 0.5 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.56 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.53 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.5 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.52 |
clpC1 | 4039655 | c.1050G>C | synonymous_variant | 0.5 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.45 |
clpC1 | 4039670 | c.1035G>T | synonymous_variant | 0.5 |
clpC1 | 4039682 | c.1023C>A | synonymous_variant | 0.53 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.46 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.49 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.51 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.55 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.55 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.53 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.53 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.53 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.51 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.54 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.55 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.58 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.6 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.62 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.6 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.6 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.59 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.61 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.61 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.67 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.68 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.67 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.71 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.72 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.57 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.61 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.63 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.63 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.6 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.59 |
clpC1 | 4039991 | c.714G>T | synonymous_variant | 0.68 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.67 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.67 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.65 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.65 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.65 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.65 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.65 |
clpC1 | 4040036 | c.669C>T | synonymous_variant | 0.65 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.52 |
clpC1 | 4040051 | c.654C>G | synonymous_variant | 0.43 |
clpC1 | 4040054 | c.651G>A | synonymous_variant | 0.43 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.4 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.35 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.33 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.25 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.25 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.25 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.25 |
clpC1 | 4040124 | p.Glu194Ser | missense_variant | 0.21 |
clpC1 | 4040141 | c.564C>T | synonymous_variant | 0.14 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.14 |
clpC1 | 4040156 | p.Met183Ile | missense_variant | 0.14 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.13 |
clpC1 | 4040166 | p.Ala180Gln | missense_variant | 0.13 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.13 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.23 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.33 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.33 |
clpC1 | 4040429 | c.274_276delTTGinsCTC | synonymous_variant | 0.33 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 0.35 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.38 |
clpC1 | 4040456 | c.249C>T | synonymous_variant | 0.38 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.33 |
clpC1 | 4040462 | c.243C>T | synonymous_variant | 0.3 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.3 |
clpC1 | 4040468 | c.237G>C | synonymous_variant | 0.32 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.32 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.33 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.33 |
clpC1 | 4040486 | c.219G>C | synonymous_variant | 0.38 |
clpC1 | 4040495 | c.210C>T | synonymous_variant | 0.42 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.5 |
clpC1 | 4040525 | c.180C>T | synonymous_variant | 0.48 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.46 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.42 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.42 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.44 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 0.44 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.37 |
clpC1 | 4040567 | c.138C>G | synonymous_variant | 0.31 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.29 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.3 |
clpC1 | 4040582 | c.123G>T | synonymous_variant | 0.25 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.27 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.29 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.25 |
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 | 0.24 |
clpC1 | 4040612 | c.93G>A | synonymous_variant | 0.28 |
clpC1 | 4040615 | c.90C>G | synonymous_variant | 0.28 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248043 | c.1530C>G | synonymous_variant | 1.0 |
aftB | 4269153 | c.-317C>T | upstream_gene_variant | 0.15 |
aftB | 4269159 | c.-323G>C | upstream_gene_variant | 0.15 |
aftB | 4269171 | c.-335C>G | upstream_gene_variant | 0.15 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.21 |
ubiA | 4269191 | p.Ser215Gly | missense_variant | 0.21 |
ubiA | 4269199 | p.Ser212Tyr | missense_variant | 0.21 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.2 |
aftB | 4269204 | c.-368G>C | upstream_gene_variant | 0.2 |
aftB | 4269213 | c.-377C>T | upstream_gene_variant | 0.21 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.2 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.2 |
aftB | 4269225 | c.-389C>T | upstream_gene_variant | 0.2 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.2 |
aftB | 4269237 | c.-401C>G | upstream_gene_variant | 0.2 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.2 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.2 |
aftB | 4269258 | c.-422C>G | upstream_gene_variant | 0.17 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408312 | c.-110C>T | upstream_gene_variant | 1.0 |