Run ID: ERR4816470
Sample name:
Date: 01-04-2023 14:26:48
Number of reads: 564431
Percentage reads mapped: 22.31
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247368 | p.Phe285Leu | missense_variant | 0.2 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6160 | c.921C>G | synonymous_variant | 0.2 |
gyrB | 6181 | c.942C>T | synonymous_variant | 0.17 |
gyrB | 6193 | c.954G>A | synonymous_variant | 0.17 |
gyrA | 6724 | c.-578G>C | upstream_gene_variant | 0.35 |
gyrA | 6727 | c.-575G>C | upstream_gene_variant | 0.37 |
gyrA | 6730 | c.-572A>C | upstream_gene_variant | 0.43 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.54 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.54 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.52 |
gyrA | 6763 | c.-539G>A | upstream_gene_variant | 0.53 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 0.53 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.59 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.61 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.63 |
gyrB | 6794 | p.Ile519Leu | missense_variant | 0.63 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.67 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.67 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.71 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.72 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.69 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.68 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.63 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.57 |
gyrA | 6889 | c.-413G>C | upstream_gene_variant | 0.59 |
gyrB | 6896 | p.Arg553Lys | missense_variant | 0.6 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.63 |
gyrA | 6916 | c.-386G>T | upstream_gene_variant | 0.56 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.56 |
gyrA | 6922 | c.-380G>C | upstream_gene_variant | 0.47 |
gyrB | 6924 | p.Phe562Tyr | missense_variant | 0.44 |
gyrA | 6926 | c.-376T>C | upstream_gene_variant | 0.44 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.38 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.3 |
gyrA | 7120 | c.-182T>C | upstream_gene_variant | 0.18 |
gyrA | 7340 | p.Asp13Glu | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760064 | c.258G>A | synonymous_variant | 0.2 |
rpoB | 760070 | c.264T>G | synonymous_variant | 0.28 |
rpoB | 760088 | c.282C>G | synonymous_variant | 0.46 |
rpoB | 760091 | c.285G>T | synonymous_variant | 0.46 |
rpoB | 760101 | c.295_297delTTGinsCTT | synonymous_variant | 0.44 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.42 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.48 |
rpoB | 760120 | p.Arg105His | missense_variant | 0.5 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.6 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.6 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.59 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.62 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.7 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.69 |
rpoB | 760184 | c.378A>C | synonymous_variant | 0.7 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.69 |
rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 0.6 |
rpoB | 760241 | c.435G>C | synonymous_variant | 0.59 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.57 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.56 |
rpoB | 760265 | p.Met153Ile | missense_variant | 0.56 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.54 |
rpoB | 760282 | p.Thr159Ser | missense_variant | 0.44 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.33 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.29 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.35 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.36 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.42 |
rpoB | 760385 | c.579G>C | synonymous_variant | 0.42 |
rpoB | 760390 | p.Ser195Thr | missense_variant | 0.46 |
rpoB | 760394 | c.588C>G | synonymous_variant | 0.5 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.54 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.58 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.58 |
rpoB | 760418 | c.612G>A | synonymous_variant | 0.57 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.57 |
rpoB | 760427 | c.621G>A | synonymous_variant | 0.57 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.62 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.72 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.62 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.6 |
rpoB | 760481 | c.675G>A | synonymous_variant | 0.56 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.58 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.54 |
rpoB | 760508 | c.702G>T | synonymous_variant | 0.48 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.47 |
rpoB | 760520 | c.714C>G | synonymous_variant | 0.36 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.37 |
rpoB | 760526 | c.720G>A | synonymous_variant | 0.37 |
rpoB | 760527 | p.Gln241Glu | missense_variant | 0.37 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.4 |
rpoB | 760533 | p.Val243Ser | missense_variant | 0.4 |
rpoB | 760541 | c.735G>T | synonymous_variant | 0.4 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.39 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.41 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.22 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.24 |
rpoB | 760616 | p.Asp270Glu | missense_variant | 0.23 |
rpoB | 760617 | p.Ile271Val | missense_variant | 0.23 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.64 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.61 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.61 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.58 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.63 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.63 |
rpoB | 760958 | c.1152G>T | synonymous_variant | 0.65 |
rpoB | 760964 | c.1158C>A | synonymous_variant | 0.65 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.65 |
rpoB | 760973 | c.1167G>T | synonymous_variant | 0.65 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.65 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.65 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.65 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.65 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.63 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.57 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.59 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.59 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.52 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.52 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.19 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.2 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.2 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.2 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.2 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.19 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.19 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.19 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.2 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.21 |
rpoB | 761159 | c.1353G>T | synonymous_variant | 0.22 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.19 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.19 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.19 |
rpoB | 761178 | c.1372_1374delTCAinsAGC | synonymous_variant | 0.19 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.35 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.38 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.38 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.48 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.5 |
rpoB | 761240 | c.1434C>T | synonymous_variant | 0.51 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.5 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.45 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.45 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.46 |
rpoB | 761300 | c.1494G>A | synonymous_variant | 0.41 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.42 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.42 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.27 |
rpoB | 761351 | c.1545C>T | synonymous_variant | 0.22 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.17 |
rpoB | 761819 | c.2013G>T | synonymous_variant | 0.17 |
rpoB | 761834 | c.2028T>G | synonymous_variant | 0.17 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.17 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.17 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.17 |
rpoB | 761863 | p.Ala686Glu | missense_variant | 0.18 |
rpoB | 761867 | c.2061C>A | synonymous_variant | 0.19 |
rpoB | 761868 | p.Asp688Gln | missense_variant | 0.19 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.19 |
rpoB | 761882 | c.2076C>A | synonymous_variant | 0.19 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.2 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.21 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.2 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.2 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.19 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.19 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.19 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.19 |
rpoB | 761930 | c.2124G>A | synonymous_variant | 0.41 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.41 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.41 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 0.56 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.57 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 0.53 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.51 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.51 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.51 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.49 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.49 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.56 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.58 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.58 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.55 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.55 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 0.55 |
rpoB | 762101 | c.2295C>T | synonymous_variant | 0.54 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.51 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.51 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.53 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.55 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.56 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 0.59 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.52 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 0.52 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.48 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.43 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.4 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.27 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.32 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.3 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.26 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.29 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.29 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.18 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.18 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.19 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.33 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.33 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.31 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.5 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 0.5 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.4 |
rpoC | 762446 | c.-924C>A | upstream_gene_variant | 0.4 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.38 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.38 |
rpoC | 762485 | c.-885G>C | upstream_gene_variant | 0.4 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.4 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.35 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.35 |
rpoC | 762524 | c.-846G>T | upstream_gene_variant | 0.25 |
rpoC | 762527 | c.-843G>C | upstream_gene_variant | 0.25 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.27 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.25 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.25 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.21 |
rpoC | 762554 | c.-816G>T | upstream_gene_variant | 0.2 |
rpoC | 762560 | c.-810A>T | upstream_gene_variant | 0.2 |
rpoC | 762563 | c.-807G>T | upstream_gene_variant | 0.2 |
rpoC | 762575 | c.-795C>T | upstream_gene_variant | 0.21 |
rpoB | 762630 | p.Ala942Thr | missense_variant | 0.18 |
rpoC | 762770 | c.-600C>G | upstream_gene_variant | 0.18 |
rpoB | 762785 | p.Asp993Glu | missense_variant | 0.25 |
rpoC | 762788 | c.-582G>C | upstream_gene_variant | 0.25 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.25 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.33 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.35 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.39 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.42 |
rpoC | 762827 | c.-543G>T | upstream_gene_variant | 0.41 |
rpoC | 762830 | c.-540C>T | upstream_gene_variant | 0.41 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.41 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.41 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.41 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.46 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.6 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.69 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.7 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.74 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.74 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.75 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.77 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.8 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.82 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.77 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.79 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.21 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.75 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.76 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.75 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.74 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.73 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.7 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.63 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.6 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.37 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.37 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.29 |
rpoC | 763187 | c.-183C>G | upstream_gene_variant | 0.16 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.16 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.16 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.45 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.48 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.59 |
rpoC | 763492 | c.123G>T | synonymous_variant | 0.62 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.78 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.78 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.8 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.77 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.7 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.66 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.62 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.62 |
rpoC | 763675 | c.306C>T | synonymous_variant | 0.57 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.56 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.52 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.52 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.52 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.53 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.57 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.62 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.72 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.75 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.79 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.79 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.72 |
rpoC | 763768 | c.399C>A | synonymous_variant | 0.72 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.72 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.69 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.62 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.67 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.62 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.4 |
rpoC | 764107 | c.738C>T | synonymous_variant | 0.25 |
rpoC | 764134 | c.765C>A | synonymous_variant | 0.48 |
rpoC | 764143 | c.774G>C | synonymous_variant | 0.52 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 0.52 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.52 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.46 |
rpoC | 764162 | p.Ile265Leu | missense_variant | 0.46 |
rpoC | 764169 | p.Asn267Thr | missense_variant | 0.52 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.56 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.57 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.54 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.54 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.58 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.59 |
rpoC | 764221 | c.852C>T | synonymous_variant | 0.57 |
rpoC | 764227 | c.858G>T | synonymous_variant | 0.58 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.68 |
rpoC | 764245 | c.876C>G | synonymous_variant | 0.69 |
rpoC | 764254 | c.885G>A | synonymous_variant | 0.71 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.69 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.66 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.66 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.61 |
rpoC | 764297 | p.Met310Leu | missense_variant | 0.67 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.69 |
rpoC | 764317 | c.948C>T | synonymous_variant | 0.69 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.67 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.61 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.57 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.54 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.53 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.51 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.51 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.44 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.34 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 0.34 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.56 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.56 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.56 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.56 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.53 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.51 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.54 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.53 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.53 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.67 |
rpoC | 764500 | c.1131C>T | synonymous_variant | 0.65 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.65 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.65 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.67 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.73 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.78 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.78 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.81 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.84 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.88 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.88 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.88 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.87 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.8 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.8 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.76 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.76 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.75 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.75 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.72 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.72 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.72 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.71 |
rpoC | 764764 | p.His465Gln | missense_variant | 0.69 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.62 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.63 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.58 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.62 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.58 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.58 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.54 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.54 |
rpoC | 764872 | c.1503A>T | synonymous_variant | 0.5 |
rpoC | 764875 | c.1506C>G | synonymous_variant | 0.49 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.47 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.54 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.54 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.57 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.54 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.54 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.55 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.55 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.62 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.62 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.67 |
rpoC | 765004 | c.1635G>T | synonymous_variant | 0.54 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.54 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.54 |
rpoC | 765013 | c.1644C>T | synonymous_variant | 0.53 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.54 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.54 |
rpoC | 765034 | c.1665T>G | synonymous_variant | 0.54 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.5 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.5 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.49 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.51 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.5 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.5 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.49 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.46 |
rpoC | 765082 | c.1713G>T | synonymous_variant | 0.47 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.47 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.49 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.44 |
rpoC | 765121 | c.1752G>T | synonymous_variant | 0.33 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.33 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.3 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.33 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.38 |
rpoC | 765499 | c.2130C>A | synonymous_variant | 0.38 |
rpoC | 765525 | p.Ala719Val | missense_variant | 0.31 |
rpoC | 765532 | c.2163C>T | synonymous_variant | 0.31 |
rpoC | 765544 | c.2175C>T | synonymous_variant | 0.27 |
rpoC | 765547 | c.2178C>T | synonymous_variant | 0.27 |
rpoC | 765548 | c.2179_2181delAGCinsTCG | synonymous_variant | 0.27 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.27 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.27 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.3 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.25 |
rpoC | 765590 | p.Arg741Ala | missense_variant | 0.23 |
rpoC | 765596 | p.Lys743Ala | missense_variant | 0.21 |
rpoC | 765844 | c.2475C>G | synonymous_variant | 0.25 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.5 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.42 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.39 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.39 |
rpoC | 765907 | c.2538G>C | synonymous_variant | 0.33 |
rpoC | 765908 | p.Leu847Ala | missense_variant | 0.33 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.35 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.3 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.3 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.23 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.22 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.26 |
rpoC | 765961 | c.2592G>A | synonymous_variant | 0.26 |
rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 0.26 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.27 |
rpoC | 765970 | c.2601C>G | synonymous_variant | 0.27 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.32 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.32 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.18 |
rpoC | 766291 | c.2922G>C | synonymous_variant | 0.17 |
rpoC | 766297 | c.2928G>C | synonymous_variant | 0.18 |
rpoC | 766299 | p.Thr977Met | missense_variant | 0.18 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 0.4 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.43 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.43 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 0.5 |
rpoC | 766333 | c.2964G>C | synonymous_variant | 0.6 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.56 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.53 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.59 |
rpoC | 766361 | p.Val998Ile | missense_variant | 0.59 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.62 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 0.59 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.56 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.56 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.59 |
rpoC | 766402 | c.3033C>G | synonymous_variant | 0.61 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.6 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.6 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.57 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.21 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.2 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.21 |
rpoC | 766612 | c.3243C>G | synonymous_variant | 0.22 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.22 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 0.22 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.24 |
rpoC | 766633 | c.3264G>C | synonymous_variant | 0.22 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.27 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.27 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.27 |
rpoC | 766660 | c.3291G>T | synonymous_variant | 0.27 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.27 |
rpoC | 766667 | p.Ser1100Ala | missense_variant | 0.27 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.29 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.39 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.39 |
rpoC | 766711 | c.3342C>T | synonymous_variant | 0.39 |
rpoC | 766717 | c.3348C>G | synonymous_variant | 0.44 |
rpoC | 766718 | p.Asp1117Asn | missense_variant | 0.44 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.44 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.36 |
rpoC | 766741 | c.3372G>C | synonymous_variant | 0.23 |
rpoC | 766742 | p.Gln1125Met | missense_variant | 0.23 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.23 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.25 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.25 |
rpoC | 766754 | p.Glu1129Gln | missense_variant | 0.25 |
rpoC | 766763 | p.Ile1132Val | missense_variant | 0.33 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.23 |
rpoC | 766775 | p.Arg1136Asn | missense_variant | 0.23 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.38 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.38 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.44 |
rpoC | 766835 | p.Val1156Thr | missense_variant | 0.39 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.4 |
rpoC | 766846 | c.3477C>T | synonymous_variant | 0.4 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 0.4 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.38 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.43 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.44 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.45 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.45 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.42 |
rpoC | 766909 | c.3540G>C | synonymous_variant | 0.4 |
rpoC | 766911 | p.Ile1181Thr | missense_variant | 0.4 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.44 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.42 |
rpoC | 766921 | c.3552G>C | synonymous_variant | 0.42 |
rpoC | 766933 | c.3564A>C | synonymous_variant | 0.36 |
rpoC | 766935 | p.Glu1189Ala | missense_variant | 0.36 |
rpoC | 766942 | c.3573C>G | synonymous_variant | 0.33 |
rpoC | 766944 | p.Arg1192Gln | missense_variant | 0.36 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.33 |
rpoC | 766952 | p.Ala1195Ser | missense_variant | 0.36 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.38 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.43 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.43 |
rpoC | 766987 | c.3618G>C | synonymous_variant | 0.5 |
rpoC | 766990 | c.3621G>C | synonymous_variant | 0.57 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.58 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.64 |
rpoC | 767008 | c.3639G>C | synonymous_variant | 0.58 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.65 |
rpoC | 767023 | p.Asp1218Glu | missense_variant | 0.67 |
rpoC | 767026 | c.3657G>C | synonymous_variant | 0.67 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.71 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.71 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.69 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.72 |
rpoC | 767087 | p.Cys1240Ser | missense_variant | 0.72 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.68 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.69 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.69 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.62 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.56 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.5 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.46 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.42 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.38 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.3 |
rpoC | 767181 | p.Ala1271Glu | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777668 | p.Ile271Met | missense_variant | 1.0 |
mmpL5 | 778684 | c.-204C>T | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.16 |
rpsL | 781670 | c.111G>C | synonymous_variant | 0.3 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.35 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.33 |
rpsL | 781706 | c.147T>C | synonymous_variant | 0.33 |
rpsL | 781709 | c.150G>T | synonymous_variant | 0.33 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.33 |
rpsL | 781725 | p.Lys56Arg | missense_variant | 0.35 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.35 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.38 |
rpsL | 781737 | p.Gln60Ser | missense_variant | 0.38 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.44 |
rpsL | 781754 | c.195G>T | synonymous_variant | 0.44 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.44 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.44 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.47 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.5 |
rpsL | 781781 | c.222G>C | synonymous_variant | 0.55 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.55 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.39 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.39 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.42 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.46 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.4 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.35 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.36 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.35 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.35 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.32 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.18 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.24 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.21 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.15 |
rplC | 800610 | c.-199_-197delCTAinsTTG | upstream_gene_variant | 0.49 |
rplC | 800615 | c.-194G>T | upstream_gene_variant | 0.49 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.5 |
rplC | 800621 | c.-188G>A | upstream_gene_variant | 0.47 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.55 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.52 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.39 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.36 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.37 |
rplC | 800693 | c.-116A>T | upstream_gene_variant | 0.35 |
rplC | 800702 | c.-107G>A | upstream_gene_variant | 0.35 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 0.35 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.34 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.34 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.34 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.37 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.36 |
atpE | 1460980 | c.-65A>G | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1471930 | n.85G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471931 | n.86G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472067 | n.222G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472068 | n.223T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472288 | n.443A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472326 | n.481T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472445 | n.601dupT | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472497 | n.652G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472841 | n.996G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472846 | n.1001_1002insA | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472849 | n.1005delT | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472960 | n.1115G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472986 | n.1141C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473694 | n.37C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473719 | n.62G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473732 | n.75G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473750 | n.93C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473811 | n.154C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1473812 | n.155G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1473828 | n.171_172insCT | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473835 | n.179delA | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473934 | n.277G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473935 | n.278C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473968 | n.311C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474116 | n.459G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474627 | n.970G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474721 | n.1064G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474722 | n.1065T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475059 | n.1404_1405delCA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475064 | n.1407G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475067 | n.1410_1411insG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475080 | n.1423G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475762 | n.2106_2108delCAA | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476029 | n.2373_2377delACCTC | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476694 | n.3037G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476699 | n.3042A>T | non_coding_transcript_exon_variant | 0.8 |
rpsA | 1833586 | c.45C>T | synonymous_variant | 0.23 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.25 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.3 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.3 |
rpsA | 1833607 | c.66T>C | synonymous_variant | 0.23 |
rpsA | 1833613 | c.72C>A | synonymous_variant | 0.23 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.23 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.25 |
rpsA | 1833623 | p.Lys28Ser | missense_variant | 0.23 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.62 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.65 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.65 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.7 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.74 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.78 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.78 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.76 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.76 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.79 |
rpsA | 1833770 | p.Asn77Ser | missense_variant | 0.79 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.79 |
rpsA | 1833782 | p.Ser81Asn | missense_variant | 0.79 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.82 |
rpsA | 1833808 | c.267G>T | synonymous_variant | 0.8 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.81 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.88 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.86 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.87 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.85 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.81 |
rpsA | 1833904 | c.363G>A | synonymous_variant | 0.8 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.8 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.84 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.84 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.83 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.84 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.81 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.82 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.82 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.83 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.84 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.85 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.82 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.81 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.8 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.79 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.67 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.62 |
rpsA | 1834108 | c.567C>A | synonymous_variant | 0.58 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.54 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.61 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.35 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.35 |
rpsA | 1834157 | c.616_618delTTGinsCTC | synonymous_variant | 0.38 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.38 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.38 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 0.38 |
rpsA | 1834172 | c.631_632insGG | frameshift_variant | 0.35 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.42 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.48 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.62 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.55 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.55 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.57 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.55 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.54 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.55 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.57 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.61 |
rpsA | 1834282 | c.741C>T | synonymous_variant | 0.62 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.62 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.62 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.71 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.73 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.73 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.73 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.77 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.79 |
rpsA | 1834357 | c.816T>G | synonymous_variant | 0.81 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.83 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.84 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.89 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.88 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.89 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.89 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.9 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.88 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.89 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.88 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.88 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.88 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.86 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.86 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.82 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.79 |
rpsA | 1834543 | c.1002C>T | synonymous_variant | 0.76 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.78 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.8 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.81 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.76 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.76 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.76 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.77 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.75 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.78 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.76 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.73 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.73 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.78 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.68 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.69 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.62 |
rpsA | 1834756 | p.Glu405Asp | missense_variant | 0.6 |
rpsA | 1834759 | c.1218A>T | synonymous_variant | 0.58 |
rpsA | 1834761 | p.Phe407Tyr | missense_variant | 0.58 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.58 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.57 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.57 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.55 |
rpsA | 1834787 | p.Ala416Asn | missense_variant | 0.55 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.53 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.58 |
rpsA | 1834813 | c.1272G>C | synonymous_variant | 0.57 |
rpsA | 1834837 | p.Met432Ile | missense_variant | 0.35 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103191 | c.-149G>A | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155659 | c.453C>G | synonymous_variant | 0.56 |
katG | 2155671 | c.441G>C | synonymous_variant | 0.64 |
katG | 2155674 | c.438G>A | synonymous_variant | 0.64 |
katG | 2155677 | c.435C>A | synonymous_variant | 0.64 |
katG | 2155680 | c.432G>A | synonymous_variant | 0.64 |
katG | 2155689 | c.421_423delTTGinsCTC | synonymous_variant | 0.6 |
katG | 2155695 | p.Ala139Val | missense_variant | 0.56 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.58 |
katG | 2155719 | c.393G>T | synonymous_variant | 0.58 |
katG | 2155722 | c.390G>T | synonymous_variant | 0.61 |
katG | 2155728 | c.384G>T | synonymous_variant | 0.56 |
katG | 2155737 | c.375C>A | synonymous_variant | 0.5 |
katG | 2155741 | p.Gly124Thr | missense_variant | 0.5 |
katG | 2155743 | c.369G>A | synonymous_variant | 0.47 |
katG | 2155749 | c.363C>A | synonymous_variant | 0.5 |
katG | 2155755 | c.357C>T | synonymous_variant | 0.5 |
katG | 2155764 | p.His116Glu | missense_variant | 0.53 |
katG | 2155769 | p.Ile115Val | missense_variant | 0.53 |
katG | 2155782 | c.330C>G | synonymous_variant | 0.53 |
katG | 2155785 | c.327T>C | synonymous_variant | 0.53 |
katG | 2155794 | p.Ala106Ser | missense_variant | 0.33 |
katG | 2155806 | c.306T>C | synonymous_variant | 0.15 |
katG | 2155811 | c.301C>T | synonymous_variant | 0.15 |
katG | 2155812 | c.300G>C | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169323 | c.1290C>G | synonymous_variant | 0.14 |
PPE35 | 2169326 | c.1287C>T | synonymous_variant | 0.17 |
PPE35 | 2169337 | p.Asp426His | missense_variant | 0.17 |
Rv1979c | 2221732 | p.Pro478Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.7 |
kasA | 2517968 | c.-147T>A | upstream_gene_variant | 0.47 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.33 |
kasA | 2517983 | c.-132T>C | upstream_gene_variant | 0.18 |
kasA | 2519176 | c.1062G>A | synonymous_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726561 | c.369T>C | synonymous_variant | 0.43 |
ahpC | 2726564 | c.372C>T | synonymous_variant | 0.5 |
ahpC | 2726576 | c.384C>T | synonymous_variant | 0.55 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.59 |
ahpC | 2726582 | c.390G>C | synonymous_variant | 0.64 |
ahpC | 2726588 | c.396C>T | synonymous_variant | 0.7 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.7 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.69 |
ahpC | 2726604 | p.Val138Ile | missense_variant | 0.71 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.79 |
ahpC | 2726651 | c.459G>T | synonymous_variant | 0.76 |
ahpC | 2726654 | c.462G>C | synonymous_variant | 0.76 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.76 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.75 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.78 |
ahpC | 2726681 | c.489A>T | synonymous_variant | 0.75 |
ahpC | 2726684 | c.492G>T | synonymous_variant | 0.78 |
ahpC | 2726693 | c.501C>A | synonymous_variant | 0.78 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.74 |
ahpC | 2726717 | c.525A>C | synonymous_variant | 0.58 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.22 |
thyX | 3067328 | c.618G>C | synonymous_variant | 0.33 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.36 |
thyX | 3067344 | p.Ser201Thr | missense_variant | 0.36 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.36 |
thyX | 3067355 | p.Ala197Gly | missense_variant | 0.36 |
thyX | 3067360 | p.Ile196Val | missense_variant | 0.4 |
thyX | 3067367 | c.579G>A | synonymous_variant | 0.44 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.4 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.4 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.33 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.38 |
thyX | 3067400 | p.Arg182Lys | missense_variant | 0.38 |
thyX | 3067429 | p.Ala173Ser | missense_variant | 0.29 |
thyX | 3067430 | c.514_516delCGCinsAGG | synonymous_variant | 0.27 |
thyX | 3067433 | c.513C>G | synonymous_variant | 0.27 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.27 |
thyX | 3067442 | c.504C>G | synonymous_variant | 0.27 |
thyX | 3067445 | c.501C>A | synonymous_variant | 0.27 |
thyX | 3068115 | c.-170C>T | upstream_gene_variant | 0.17 |
thyA | 3073935 | c.537C>A | synonymous_variant | 0.17 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473977 | c.-30C>G | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640368 | c.-175A>G | upstream_gene_variant | 0.22 |
rpoA | 3877545 | c.963G>C | synonymous_variant | 0.13 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.4 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.43 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 0.5 |
rpoA | 3877569 | p.Pro313Ala | missense_variant | 0.56 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.59 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.59 |
rpoA | 3877599 | p.Gln303Thr | missense_variant | 0.59 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.69 |
rpoA | 3877629 | c.879C>G | synonymous_variant | 0.73 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.73 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.7 |
rpoA | 3877665 | c.843C>T | synonymous_variant | 0.66 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.65 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.67 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.67 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.69 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.68 |
rpoA | 3877701 | c.807G>C | synonymous_variant | 0.7 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.7 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.7 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.69 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.7 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.71 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.69 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.7 |
rpoA | 3877765 | p.Ala248Ser | missense_variant | 0.67 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.65 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.66 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.65 |
rpoA | 3877785 | c.723C>T | synonymous_variant | 0.67 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.64 |
rpoA | 3877794 | c.714G>T | synonymous_variant | 0.64 |
rpoA | 3877815 | c.693C>A | synonymous_variant | 0.65 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.69 |
rpoA | 3877821 | c.687C>T | synonymous_variant | 0.65 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.69 |
rpoA | 3877842 | c.666A>T | synonymous_variant | 0.67 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.67 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.62 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.66 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.61 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.59 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.56 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.56 |
rpoA | 3877896 | p.Pro204Ala | missense_variant | 0.55 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.5 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.51 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.5 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.46 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.46 |
rpoA | 3877935 | p.Lys191Arg | missense_variant | 0.47 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.5 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.5 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.32 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.31 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 0.31 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.17 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.19 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.19 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.18 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.21 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.24 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.16 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.24 |
rpoA | 3878214 | c.294C>T | synonymous_variant | 0.36 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.36 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.38 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.37 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.36 |
rpoA | 3878251 | c.256_257delTCinsAG | synonymous_variant | 0.38 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.36 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.36 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.33 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.33 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.27 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.27 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.24 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.23 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.23 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.21 |
rpoA | 3878331 | c.177A>T | synonymous_variant | 0.17 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.24 |
clpC1 | 4038383 | c.2322G>T | synonymous_variant | 0.22 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.22 |
clpC1 | 4038395 | c.2310C>G | synonymous_variant | 0.2 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.18 |
clpC1 | 4038404 | c.2301G>T | synonymous_variant | 0.18 |
clpC1 | 4038410 | c.2295C>T | synonymous_variant | 0.18 |
clpC1 | 4038416 | c.2289C>G | synonymous_variant | 0.19 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.17 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.22 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.3 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.61 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.61 |
clpC1 | 4038743 | c.1962G>C | synonymous_variant | 0.61 |
clpC1 | 4038746 | c.1959C>T | synonymous_variant | 0.64 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.72 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.71 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.76 |
clpC1 | 4038770 | c.1935C>A | synonymous_variant | 0.76 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.8 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.81 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.83 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.84 |
clpC1 | 4038810 | p.Gln632Ser | missense_variant | 0.82 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.82 |
clpC1 | 4038815 | c.1890G>A | synonymous_variant | 0.85 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.86 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.86 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.82 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.81 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.81 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.81 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.83 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.8 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.79 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.78 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.78 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.78 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.76 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.77 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.77 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.78 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.78 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.79 |
clpC1 | 4039007 | c.1698G>C | synonymous_variant | 0.79 |
clpC1 | 4039019 | c.1686G>C | synonymous_variant | 0.77 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.78 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.82 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.8 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.8 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.79 |
clpC1 | 4039106 | c.1599G>T | synonymous_variant | 0.78 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.78 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.77 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.77 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.75 |
clpC1 | 4039139 | c.1566G>A | synonymous_variant | 0.73 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.73 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.73 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.71 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.7 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.67 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.65 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.66 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.65 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.6 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.53 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.46 |
clpC1 | 4039244 | c.1461G>T | synonymous_variant | 0.44 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.23 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.3 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.29 |
clpC1 | 4039394 | c.1309_1311delTCGinsAGC | synonymous_variant | 0.27 |
clpC1 | 4039407 | p.Arg433Lys | missense_variant | 0.26 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.26 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.27 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.27 |
clpC1 | 4039424 | p.Lys427Arg | missense_variant | 0.26 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.25 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.26 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.24 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.24 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.24 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.25 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.29 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.27 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.26 |
clpC1 | 4039487 | c.1218G>A | synonymous_variant | 0.27 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.33 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.34 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.34 |
clpC1 | 4039544 | c.1161C>T | synonymous_variant | 0.36 |
clpC1 | 4039550 | c.1155G>T | synonymous_variant | 0.36 |
clpC1 | 4039556 | c.1149G>A | synonymous_variant | 0.37 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.38 |
clpC1 | 4039562 | c.1143C>T | synonymous_variant | 0.37 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.36 |
clpC1 | 4039568 | p.Met379Leu | missense_variant | 0.36 |
clpC1 | 4039571 | c.1134G>T | synonymous_variant | 0.36 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.37 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.37 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.47 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.49 |
clpC1 | 4039603 | p.Ala368Thr | missense_variant | 0.69 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.7 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.74 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.74 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.66 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.61 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.59 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.64 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.64 |
clpC1 | 4039694 | c.1011G>A | synonymous_variant | 0.62 |
clpC1 | 4039697 | c.1008C>A | synonymous_variant | 0.66 |
clpC1 | 4039721 | c.984C>T | synonymous_variant | 0.68 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.68 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.67 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.58 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.57 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.54 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.52 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.48 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.48 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.48 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.48 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.35 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.35 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.38 |
clpC1 | 4039802 | c.903G>A | synonymous_variant | 0.47 |
clpC1 | 4039811 | c.894C>A | synonymous_variant | 0.57 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.57 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.57 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.57 |
clpC1 | 4039832 | c.873C>A | synonymous_variant | 0.57 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.59 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.74 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.67 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.7 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.63 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.63 |
clpC1 | 4039934 | c.771G>A | synonymous_variant | 0.63 |
clpC1 | 4039937 | c.768G>T | synonymous_variant | 0.63 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.63 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.62 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.57 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.53 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.59 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.56 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.56 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.53 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.52 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.5 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.56 |
clpC1 | 4040062 | p.Ile215Val | missense_variant | 0.6 |
clpC1 | 4040066 | c.639G>T | synonymous_variant | 0.39 |
clpC1 | 4040069 | c.636G>T | synonymous_variant | 0.4 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.36 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.27 |
clpC1 | 4040120 | c.585G>A | synonymous_variant | 0.26 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.19 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.24 |
clpC1 | 4040282 | c.423G>C | synonymous_variant | 0.28 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.38 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.38 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.42 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.42 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.42 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.42 |
clpC1 | 4040336 | c.369G>T | synonymous_variant | 0.38 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.41 |
clpC1 | 4040348 | c.357G>T | synonymous_variant | 0.41 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.39 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.42 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.45 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.49 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.47 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.47 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.6 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.62 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.75 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.72 |
clpC1 | 4040432 | c.271_273delAGCinsTCG | synonymous_variant | 0.7 |
clpC1 | 4040437 | c.268C>T | synonymous_variant | 0.71 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.77 |
clpC1 | 4040456 | c.249C>T | synonymous_variant | 0.75 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.75 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.75 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.75 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.76 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.78 |
clpC1 | 4040495 | c.210C>T | synonymous_variant | 0.8 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.8 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.8 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.79 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.79 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.81 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.76 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.67 |
clpC1 | 4040552 | c.153G>T | synonymous_variant | 0.67 |
clpC1 | 4040563 | p.Ser48Ala | missense_variant | 0.6 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.56 |
clpC1 | 4040582 | c.123G>T | synonymous_variant | 0.56 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.51 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.51 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.5 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.5 |
clpC1 | 4040603 | c.102T>C | synonymous_variant | 0.49 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.5 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.41 |
clpC1 | 4040645 | c.60C>G | synonymous_variant | 0.39 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.33 |
clpC1 | 4040657 | c.48T>C | synonymous_variant | 0.28 |
clpC1 | 4040663 | c.42C>T | synonymous_variant | 0.18 |
embC | 4241689 | c.1827G>A | synonymous_variant | 0.29 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244137 | p.Ala302Val | missense_variant | 0.17 |
embB | 4246094 | c.-420C>T | upstream_gene_variant | 0.14 |
aftB | 4267096 | p.Pro581Thr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408380 | c.-178G>A | upstream_gene_variant | 0.2 |