Run ID: ERR4796577
Sample name:
Date: 01-04-2023 06:57:00
Number of reads: 1003782
Percentage reads mapped: 25.0
Strain:
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.98 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.32 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.67 | streptomycin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.44 | streptomycin |
fabG1 | 1673424 | c.-16A>G | upstream_gene_variant | 1.0 | isoniazid |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674263 | p.Ile21Thr | missense_variant | 1.0 | isoniazid, ethionamide |
katG | 2155179 | p.Asp311Glu | missense_variant | 0.22 | isoniazid |
pncA | 2288703 | p.Val180Ala | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 5771 | p.Ala178Thr | missense_variant | 0.17 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.88 |
gyrB | 6151 | c.912C>T | synonymous_variant | 0.22 |
gyrB | 6157 | c.918C>T | synonymous_variant | 0.22 |
gyrB | 6160 | c.921C>G | synonymous_variant | 0.22 |
gyrB | 6169 | c.930C>G | synonymous_variant | 0.27 |
gyrB | 6172 | c.933C>T | synonymous_variant | 0.27 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.43 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.43 |
gyrB | 6663 | p.Phe475Tyr | missense_variant | 0.67 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.57 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.57 |
gyrB | 6680 | p.Leu481Ile | missense_variant | 0.56 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.67 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.67 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.67 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.67 |
gyrA | 6733 | c.-569G>A | upstream_gene_variant | 0.67 |
gyrA | 6739 | c.-563C>G | upstream_gene_variant | 0.67 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.65 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.65 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.67 |
gyrA | 6754 | c.-548C>T | upstream_gene_variant | 0.71 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.71 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 0.68 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.59 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.45 |
gyrB | 6794 | p.Ile519Leu | missense_variant | 0.45 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.45 |
gyrA | 6805 | c.-497G>C | upstream_gene_variant | 0.45 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.45 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.38 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.4 |
gyrA | 6850 | c.-452C>G | upstream_gene_variant | 0.37 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.37 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.37 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.37 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.37 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.33 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.33 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.33 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.32 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.27 |
gyrB | 6911 | p.Asn558His | missense_variant | 0.24 |
gyrA | 6916 | c.-386G>C | upstream_gene_variant | 0.28 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.29 |
gyrB | 6924 | p.Phe562Tyr | missense_variant | 0.28 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.29 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.29 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.28 |
gyrA | 6955 | c.-347G>A | upstream_gene_variant | 0.27 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.14 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 0.22 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.26 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.35 |
gyrA | 7081 | c.-221T>C | upstream_gene_variant | 0.35 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.35 |
gyrB | 7088 | p.Asp617Asn | missense_variant | 0.37 |
gyrA | 7093 | c.-209T>C | upstream_gene_variant | 0.33 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.42 |
gyrA | 7100 | c.-202T>C | upstream_gene_variant | 0.42 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.42 |
gyrB | 7124 | p.Ser629Glu | missense_variant | 0.48 |
gyrA | 7129 | c.-173T>C | upstream_gene_variant | 0.44 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.44 |
gyrA | 7136 | c.-166T>C | upstream_gene_variant | 0.44 |
gyrA | 7144 | c.-158A>G | upstream_gene_variant | 0.44 |
gyrA | 7147 | c.-155G>C | upstream_gene_variant | 0.42 |
gyrA | 7150 | c.-152G>C | upstream_gene_variant | 0.42 |
gyrA | 7153 | c.-149G>C | upstream_gene_variant | 0.42 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.44 |
gyrA | 7177 | c.-125G>A | upstream_gene_variant | 0.46 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.46 |
gyrA | 7190 | c.-112C>T | upstream_gene_variant | 0.46 |
gyrA | 7198 | c.-104C>G | upstream_gene_variant | 0.43 |
gyrB | 7209 | p.Asp657Ala | missense_variant | 0.47 |
gyrA | 7213 | c.-89G>A | upstream_gene_variant | 0.44 |
gyrA | 7216 | c.-86G>T | upstream_gene_variant | 0.44 |
gyrB | 7229 | p.Thr664Ala | missense_variant | 0.38 |
gyrA | 7243 | c.-59G>A | upstream_gene_variant | 0.4 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
gyrA | 7334 | c.33G>A | synonymous_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8315 | c.1014G>A | synonymous_variant | 0.38 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.44 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.44 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.44 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.6 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.57 |
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.57 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.57 |
gyrA | 8401 | p.Asp367Ala | missense_variant | 0.57 |
gyrA | 8408 | c.1107A>G | synonymous_variant | 0.57 |
gyrA | 8409 | p.Leu370Ile | missense_variant | 0.57 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
gyrA | 8426 | c.1125G>C | synonymous_variant | 1.0 |
gyrA | 8433 | p.Thr378Arg | missense_variant | 1.0 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.75 |
gyrA | 8454 | p.Asn385Glu | missense_variant | 0.67 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.67 |
gyrA | 8468 | c.1167C>T | synonymous_variant | 0.5 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.5 |
gyrA | 8480 | c.1179C>A | synonymous_variant | 0.5 |
gyrA | 8486 | c.1185T>G | synonymous_variant | 0.4 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.4 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.4 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.19 |
gyrA | 8780 | c.1479C>T | synonymous_variant | 0.32 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.32 |
gyrA | 8790 | p.Arg497Lys | missense_variant | 0.32 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.43 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.45 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.6 |
gyrA | 8846 | c.1545C>T | synonymous_variant | 0.67 |
gyrA | 8849 | c.1548C>G | synonymous_variant | 0.7 |
gyrA | 8852 | c.1551T>G | synonymous_variant | 0.7 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.7 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.72 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.75 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.76 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.83 |
gyrA | 8913 | p.Lys538Arg | missense_variant | 0.88 |
gyrA | 8921 | c.1620C>T | synonymous_variant | 0.85 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.9 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.89 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.89 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.91 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.91 |
gyrA | 8982 | p.Cys561Ser | missense_variant | 0.91 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.91 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.91 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.88 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.88 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.86 |
gyrA | 9023 | c.1722A>T | synonymous_variant | 0.86 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.86 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.86 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.82 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.64 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.64 |
gyrA | 9063 | p.Ser588Asn | missense_variant | 0.55 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.55 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.6 |
gyrA | 9074 | c.1773G>C | synonymous_variant | 0.6 |
gyrA | 9080 | c.1779G>A | synonymous_variant | 0.6 |
gyrA | 9092 | c.1791C>G | synonymous_variant | 0.56 |
gyrA | 9099 | c.1798T>C | synonymous_variant | 0.44 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9576 | p.Arg759Ser | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.62 |
mshA | 576295 | c.948C>T | synonymous_variant | 0.2 |
ccsA | 620852 | p.Ala321Val | missense_variant | 0.18 |
rpoB | 760070 | c.264T>C | synonymous_variant | 0.32 |
rpoB | 760091 | c.285G>A | synonymous_variant | 0.45 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.59 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.59 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.59 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.62 |
rpoB | 760120 | p.Arg105His | missense_variant | 0.62 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.75 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.76 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.73 |
rpoB | 760145 | c.339C>G | synonymous_variant | 0.78 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.78 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.82 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.79 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.79 |
rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 0.7 |
rpoB | 760241 | c.435G>C | synonymous_variant | 0.7 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.64 |
rpoB | 760265 | p.Met153Ile | missense_variant | 0.65 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.52 |
rpoB | 760282 | p.Thr159Ser | missense_variant | 0.48 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.35 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.31 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.17 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.18 |
rpoB | 760354 | p.Glu183Ala | missense_variant | 0.25 |
rpoB | 760356 | p.Thr184Ala | missense_variant | 0.4 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.38 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.38 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.38 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.38 |
rpoB | 760390 | p.Ser195Thr | missense_variant | 0.38 |
rpoB | 760394 | c.588C>G | synonymous_variant | 0.4 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.46 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.46 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.5 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.8 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.8 |
rpoB | 760472 | c.666C>T | synonymous_variant | 0.82 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.81 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.77 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.81 |
rpoB | 760496 | c.690G>A | synonymous_variant | 0.88 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.8 |
rpoB | 760515 | p.Trp237Met | missense_variant | 0.8 |
rpoB | 760522 | p.Ser239Thr | missense_variant | 0.71 |
rpoB | 760527 | p.Gln241Glu | missense_variant | 0.71 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.71 |
rpoB | 760534 | p.Val243Ala | missense_variant | 0.71 |
rpoB | 760538 | p.Glu244Asp | missense_variant | 0.75 |
rpoB | 760547 | c.741G>A | synonymous_variant | 0.71 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.58 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.58 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.57 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.71 |
rpoB | 760616 | p.Asp270Glu | missense_variant | 0.71 |
rpoB | 760617 | p.Ile271Val | missense_variant | 0.71 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.71 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.71 |
rpoB | 760640 | c.834C>T | synonymous_variant | 0.71 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.71 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.71 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.74 |
rpoB | 760665 | p.Gln287Glu | missense_variant | 0.74 |
rpoB | 760669 | p.Thr288Asn | missense_variant | 0.74 |
rpoB | 760673 | c.867G>T | synonymous_variant | 0.77 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.77 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.77 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.77 |
rpoB | 760715 | c.909C>G | synonymous_variant | 0.68 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.65 |
rpoB | 760727 | c.921C>G | synonymous_variant | 0.62 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.62 |
rpoB | 760734 | p.Val310Ile | missense_variant | 0.62 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.23 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.23 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.29 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.31 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.37 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.38 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.42 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.5 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.5 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.5 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.52 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.69 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.77 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.75 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.75 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.74 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.77 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.76 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.76 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.82 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.81 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.85 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.73 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.77 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.73 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.72 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.57 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.53 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.5 |
rpoB | 761178 | c.1372_1374delTCAinsAGC | synonymous_variant | 0.53 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.53 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.5 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.52 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.55 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.57 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.57 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.52 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.52 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.52 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.52 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.52 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.5 |
rpoB | 761282 | c.1476C>G | synonymous_variant | 0.48 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.33 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.33 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.21 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.2 |
rpoB | 761529 | p.Val575Ile | missense_variant | 0.36 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.62 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.63 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.7 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.7 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.76 |
rpoB | 761603 | c.1797C>A | synonymous_variant | 0.76 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.76 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.84 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.76 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.76 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.76 |
rpoB | 761650 | p.Ser615Asn | missense_variant | 0.73 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.73 |
rpoB | 761666 | c.1860G>T | synonymous_variant | 0.76 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.7 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.38 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.33 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.33 |
rpoB | 761694 | p.Ile630Val | missense_variant | 0.33 |
rpoB | 761705 | c.1899C>T | synonymous_variant | 0.25 |
rpoB | 761711 | c.1905C>G | synonymous_variant | 0.25 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.32 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.3 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.3 |
rpoB | 761789 | c.1983G>C | synonymous_variant | 0.29 |
rpoB | 761790 | p.Arg662Asp | missense_variant | 0.29 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.48 |
rpoB | 761816 | c.2010C>G | synonymous_variant | 0.48 |
rpoB | 761819 | c.2013G>C | synonymous_variant | 0.46 |
rpoB | 761834 | c.2028T>G | synonymous_variant | 0.56 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.59 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.57 |
rpoB | 761863 | p.Ala686Glu | missense_variant | 0.61 |
rpoB | 761868 | p.Asp688Gln | missense_variant | 0.62 |
rpoB | 761873 | c.2067A>T | synonymous_variant | 0.62 |
rpoB | 761891 | c.2085G>A | synonymous_variant | 0.62 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.62 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.6 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.56 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.57 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.59 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 0.68 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 0.76 |
rpoB | 761942 | c.2136C>T | synonymous_variant | 0.8 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.76 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.76 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.88 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 0.9 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.9 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.9 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.95 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.95 |
rpoB | 762024 | p.Val740Thr | missense_variant | 0.91 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.85 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.81 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.8 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.73 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.71 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.76 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.76 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.76 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.76 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.77 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.77 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.82 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.83 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.84 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.89 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.84 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.84 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.85 |
rpoB | 762269 | c.2463G>A | synonymous_variant | 0.86 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.9 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.84 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 0.83 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.8 |
rpoB | 762335 | c.2529C>T | synonymous_variant | 0.76 |
rpoB | 762336 | p.Ile844Val | missense_variant | 0.75 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.83 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.79 |
rpoB | 762348 | c.2542_2543delTCinsAG | synonymous_variant | 0.79 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.84 |
rpoB | 762368 | p.Glu854Asp | missense_variant | 0.84 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.84 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.85 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.86 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.88 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.88 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.82 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.82 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 0.71 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.68 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.64 |
rpoC | 762485 | c.-885G>C | upstream_gene_variant | 0.64 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.61 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.59 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.59 |
rpoC | 762527 | c.-843G>C | upstream_gene_variant | 0.57 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.5 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.44 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.44 |
rpoC | 762545 | c.-825C>G | upstream_gene_variant | 0.47 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.42 |
rpoC | 762581 | c.-789T>C | upstream_gene_variant | 0.22 |
rpoC | 762582 | c.-788T>C | upstream_gene_variant | 0.22 |
rpoC | 762587 | c.-783G>A | upstream_gene_variant | 0.2 |
rpoB | 762595 | c.2789_2790insC | frameshift_variant | 0.17 |
rpoC | 762626 | c.-744C>T | upstream_gene_variant | 0.22 |
rpoC | 762776 | c.-594C>T | upstream_gene_variant | 0.5 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.63 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.68 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.68 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.68 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.71 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.71 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.73 |
rpoC | 762830 | c.-540C>T | upstream_gene_variant | 0.76 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.76 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.69 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.65 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.67 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.7 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.7 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.71 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.74 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.76 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.75 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.71 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.72 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.74 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.78 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.87 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.86 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.86 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.87 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.89 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.88 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.88 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.87 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.96 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 1.0 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.9 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.86 |
rpoC | 763447 | c.78C>T | synonymous_variant | 0.18 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.44 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.55 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.56 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.74 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.75 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.71 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.74 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.69 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.72 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.75 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.75 |
rpoC | 763648 | c.279C>G | synonymous_variant | 0.71 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.76 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.76 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.8 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.8 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.8 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.86 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.86 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.86 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.86 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.86 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.85 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.79 |
rpoC | 763786 | c.417C>G | synonymous_variant | 0.74 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.73 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.72 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.59 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.55 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.47 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764134 | c.765C>G | synonymous_variant | 0.47 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.47 |
rpoC | 764143 | c.774G>C | synonymous_variant | 0.47 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 0.5 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.52 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.5 |
rpoC | 764162 | p.Ile265Leu | missense_variant | 0.48 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.65 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.59 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.61 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.66 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.66 |
rpoC | 764216 | p.Asn283Ser | missense_variant | 0.66 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.71 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.71 |
rpoC | 764245 | c.876C>G | synonymous_variant | 0.71 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.78 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.79 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.78 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.82 |
rpoC | 764297 | p.Met310Leu | missense_variant | 0.82 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.85 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.83 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.82 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.79 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.79 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.83 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.84 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.83 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.83 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.83 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.83 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.88 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.88 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.84 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.82 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.79 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.86 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.88 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.92 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.89 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.94 |
rpoC | 764573 | c.1204_1206delCTTinsTTG | synonymous_variant | 0.91 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.91 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.89 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.82 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.81 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.78 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.78 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.79 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.79 |
rpoC | 764690 | p.Cys441Ala | missense_variant | 0.67 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.69 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.74 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.74 |
rpoC | 764763 | p.His465Leu | missense_variant | 0.73 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.72 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.74 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 0.74 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.72 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.74 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.74 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.87 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.88 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.83 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.73 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.73 |
rpoC | 764875 | c.1506C>G | synonymous_variant | 0.73 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.65 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.65 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.65 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.65 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.65 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.6 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.6 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.56 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.56 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.69 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.52 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.6 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.66 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.68 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.59 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.61 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.61 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.61 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.61 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.61 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.61 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.61 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.61 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.61 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.62 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.61 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.62 |
rpoC | 765082 | c.1713G>A | synonymous_variant | 0.62 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.64 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.54 |
rpoC | 765121 | c.1752G>T | synonymous_variant | 0.47 |
rpoC | 765357 | p.Met663Thr | missense_variant | 0.18 |
rpoC | 765361 | c.1992C>G | synonymous_variant | 0.18 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.56 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.59 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.68 |
rpoC | 765408 | p.Gly680Glu | missense_variant | 0.71 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.74 |
rpoC | 765417 | p.Phe683Tyr | missense_variant | 0.74 |
rpoC | 765425 | p.Lys686Glu | missense_variant | 0.74 |
rpoC | 765435 | p.His689Pro | missense_variant | 0.74 |
rpoC | 765443 | p.Val692Arg | missense_variant | 0.85 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.86 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.77 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.72 |
rpoC | 765496 | c.2127C>G | synonymous_variant | 0.75 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.75 |
rpoC | 765525 | p.Ala719Val | missense_variant | 0.63 |
rpoC | 765547 | c.2178C>G | synonymous_variant | 0.2 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.25 |
rpoC | 765856 | c.2487T>C | synonymous_variant | 0.33 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.42 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.42 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.48 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.46 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.46 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.52 |
rpoC | 765908 | p.Leu847Ala | missense_variant | 0.52 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.52 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.52 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.52 |
rpoC | 765940 | c.2571A>C | synonymous_variant | 0.52 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.52 |
rpoC | 765947 | c.2578_2580delTTGinsCTC | synonymous_variant | 0.52 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.5 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.52 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.38 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.38 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.31 |
rpoC | 766148 | p.Thr927Ala | missense_variant | 0.33 |
rpoC | 766164 | p.Glu932Ala | missense_variant | 0.56 |
rpoC | 766167 | p.Ala933Asp | missense_variant | 0.56 |
rpoC | 766189 | c.2820T>C | synonymous_variant | 0.44 |
rpoC | 766192 | c.2823T>C | synonymous_variant | 0.44 |
rpoC | 766195 | p.Gln942His | missense_variant | 0.5 |
rpoC | 766207 | c.2838T>C | synonymous_variant | 0.5 |
rpoC | 766212 | p.Glu948Ala | missense_variant | 0.4 |
rpoC | 766216 | c.2847T>C | synonymous_variant | 0.4 |
rpoC | 766219 | p.Asp950Glu | missense_variant | 0.4 |
rpoC | 766222 | c.2853T>G | synonymous_variant | 0.4 |
rpoC | 766226 | c.2857_2859delTTGinsCTC | synonymous_variant | 0.4 |
rpoC | 766230 | p.Ala954Gly | missense_variant | 0.4 |
rpoC | 766234 | c.2865T>C | synonymous_variant | 0.4 |
rpoC | 766237 | c.2868T>C | synonymous_variant | 0.4 |
rpoC | 766240 | c.2871T>C | synonymous_variant | 0.4 |
rpoC | 766244 | p.Gln959Glu | missense_variant | 0.4 |
rpoC | 766267 | c.2898G>C | synonymous_variant | 0.6 |
rpoC | 766270 | c.2901G>C | synonymous_variant | 0.6 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 0.79 |
rpoC | 766288 | c.2919C>T | synonymous_variant | 0.77 |
rpoC | 766299 | p.Thr977Met | missense_variant | 0.77 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.74 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.74 |
rpoC | 766333 | c.2964G>C | synonymous_variant | 0.79 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.8 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.8 |
rpoC | 766361 | p.Val998Ile | missense_variant | 0.8 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.8 |
rpoC | 766369 | c.3000C>A | synonymous_variant | 0.8 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 0.8 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.8 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.83 |
rpoC | 766387 | c.3018C>G | synonymous_variant | 0.83 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.83 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.83 |
rpoC | 766432 | c.3063T>C | synonymous_variant | 0.65 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.65 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.45 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.45 |
rpoC | 766468 | c.3099G>A | synonymous_variant | 0.29 |
rpoC | 766618 | c.3249G>C | synonymous_variant | 0.23 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.3 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.3 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.33 |
rpoC | 766652 | c.3283_3284delTCinsAG | synonymous_variant | 0.33 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.3 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.27 |
rpoC | 766667 | p.Ser1100Ala | missense_variant | 0.3 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.3 |
rpoC | 766684 | c.3315C>G | synonymous_variant | 0.5 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.58 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.59 |
rpoC | 766718 | p.Asp1117Asn | missense_variant | 0.65 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.68 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.7 |
rpoC | 766742 | p.Gln1125Met | missense_variant | 0.7 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.68 |
rpoC | 766754 | p.Glu1129Gln | missense_variant | 0.7 |
rpoC | 766763 | p.Ile1132Val | missense_variant | 0.73 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.71 |
rpoC | 766775 | p.Arg1136Asn | missense_variant | 0.71 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.71 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.71 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.71 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.75 |
rpoC | 766835 | p.Val1156Thr | missense_variant | 0.62 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.62 |
rpoC | 766846 | c.3477C>T | synonymous_variant | 0.62 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.67 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.5 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.73 |
rpoC | 766951 | c.3582G>C | synonymous_variant | 0.79 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.92 |
rpoC | 766969 | c.3600C>G | synonymous_variant | 0.81 |
rpoC | 766990 | c.3621G>C | synonymous_variant | 0.87 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.83 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.83 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.85 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.85 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.85 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.83 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.83 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.85 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.87 |
rpoC | 767087 | p.Cys1240Ser | missense_variant | 0.84 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.84 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.83 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.83 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.83 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.81 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.68 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.67 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.62 |
rpoC | 767185 | c.3816G>T | synonymous_variant | 0.55 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.5 |
rpoC | 767203 | c.3834C>G | synonymous_variant | 0.38 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776743 | p.Pro580Ser | missense_variant | 0.18 |
mmpL5 | 776926 | p.Thr519Ala | missense_variant | 0.17 |
mmpL5 | 777589 | p.Ala298Ser | missense_variant | 0.2 |
mmpS5 | 779625 | c.-720G>A | upstream_gene_variant | 1.0 |
mmpS5 | 779639 | c.-734C>T | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781622 | c.63C>G | synonymous_variant | 0.43 |
rpsL | 781625 | c.66G>C | synonymous_variant | 0.43 |
rpsL | 781628 | c.69T>G | synonymous_variant | 0.43 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.55 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.44 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.44 |
rpsL | 781679 | c.120C>G | synonymous_variant | 0.33 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.33 |
rpsL | 781685 | c.126G>C | synonymous_variant | 0.33 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.3 |
rpsL | 781703 | c.144G>A | synonymous_variant | 0.3 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.3 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.3 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.3 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.3 |
rpsL | 781725 | p.Lys56Arg | missense_variant | 0.3 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.25 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.25 |
rpsL | 781737 | p.Gln60Gly | missense_variant | 0.23 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.33 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.41 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.44 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.42 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.44 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.44 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.44 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.42 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.42 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.36 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.36 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.34 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.33 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.33 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.3 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.32 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.33 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.29 |
rpsL | 781906 | c.348T>C | synonymous_variant | 0.22 |
rplC | 800630 | c.-179G>C | upstream_gene_variant | 0.2 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.2 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 0.29 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.29 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.33 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.33 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.32 |
rplC | 800675 | c.-134G>A | upstream_gene_variant | 0.35 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.35 |
rplC | 800702 | c.-107G>A | upstream_gene_variant | 0.31 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 0.31 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.31 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.31 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.33 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.31 |
rplC | 800738 | c.-71T>G | upstream_gene_variant | 0.31 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.33 |
rplC | 800768 | c.-41C>G | upstream_gene_variant | 0.27 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.27 |
Rv1258c | 1406596 | p.Lys249Glu | missense_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.66 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1471928 | n.83T>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1471980 | n.135G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1471981 | n.136C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472029 | n.184C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472040 | n.195T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472055 | n.211delG | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472060 | n.215T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472067 | n.222G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472106 | n.261G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472287 | n.442C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472288 | n.443A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472289 | n.444T>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472304 | n.461_471delTCTCTCGGATT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472325 | n.480G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472326 | n.481T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472327 | n.482G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472445 | n.601dupT | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472463 | n.618G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472497 | n.652G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.99 |
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 | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.95 |
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 | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.9 |
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 | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472960 | n.1115G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472986 | n.1141C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.87 |
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 | 0.96 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473719 | n.62G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473732 | n.75G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473750 | n.93C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473939 | n.282C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473946 | n.289A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473964 | n.307T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473968 | n.311C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473980 | n.323A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474116 | n.459G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474253 | n.596A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474638 | n.981C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474675 | n.1018C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474721 | n.1064G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475065 | n.1408G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475066 | n.1409C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475067 | n.1410A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475079 | n.1422T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475080 | n.1423G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475081 | n.1424C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475201 | n.1544G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475212 | n.1555A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475220 | n.1563G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475221 | n.1564C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475222 | n.1565G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475239 | n.1582A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475242 | n.1585G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475381 | n.1724G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475403 | n.1746T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475404 | n.1747A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475427 | n.1772delG | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475433 | n.1776A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475440 | n.1783T>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475443 | n.1786G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475444 | n.1787G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475485 | n.1828C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475772 | n.2115A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476524 | n.2867_2868insT | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476531 | n.2874T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476685 | n.3028A>C | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1833474 | c.-68C>G | upstream_gene_variant | 0.17 |
rpsA | 1833571 | c.30A>G | synonymous_variant | 0.29 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.25 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.27 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.29 |
rpsA | 1833613 | c.72C>T | synonymous_variant | 0.29 |
rpsA | 1833616 | c.75A>G | synonymous_variant | 0.31 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.31 |
rpsA | 1833623 | p.Lys28Ser | missense_variant | 0.31 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.45 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.55 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.6 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.6 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.58 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.6 |
rpsA | 1833697 | c.156C>A | synonymous_variant | 0.6 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.6 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.63 |
rpsA | 1833712 | c.171C>T | synonymous_variant | 0.63 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.63 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.69 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.72 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.76 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.7 |
rpsA | 1833782 | p.Ser81Asn | missense_variant | 0.7 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.72 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.78 |
rpsA | 1833817 | c.276C>T | synonymous_variant | 0.76 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.79 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.82 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.83 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.83 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.89 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.89 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.87 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.88 |
rpsA | 1833894 | p.Ala118Asp | missense_variant | 0.88 |
rpsA | 1833898 | c.357C>G | synonymous_variant | 0.88 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.94 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.85 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.86 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.87 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.87 |
rpsA | 1833997 | c.456G>A | synonymous_variant | 0.87 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.87 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.86 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.86 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.86 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.84 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.83 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.74 |
rpsA | 1834129 | c.588C>G | synonymous_variant | 0.71 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.65 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.59 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.59 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.57 |
rpsA | 1834164 | c.623_624insGGGGC | frameshift_variant | 0.57 |
rpsA | 1834167 | c.627_631delCACCA | frameshift_variant | 0.59 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.68 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.68 |
rpsA | 1834192 | c.651C>G | synonymous_variant | 0.7 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.78 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.76 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.75 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.78 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.78 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.78 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.76 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.76 |
rpsA | 1834282 | c.741C>T | synonymous_variant | 0.76 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.73 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.73 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.69 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.67 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.66 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.68 |
rpsA | 1834357 | c.816T>G | synonymous_variant | 0.59 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.56 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.56 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.56 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.56 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.56 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.58 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 0.59 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.6 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 0.58 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.6 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.7 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.74 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.74 |
rpsA | 1834477 | c.936C>A | synonymous_variant | 0.74 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.74 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.76 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.75 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.83 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.85 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.86 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.86 |
rpsA | 1834556 | p.Ala339Ser | missense_variant | 0.86 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.79 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.78 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.8 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.81 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.81 |
rpsA | 1834657 | c.1116G>A | synonymous_variant | 0.83 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.84 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.76 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.79 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.78 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 0.67 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.71 |
rpsA | 1834756 | c.1215G>A | synonymous_variant | 0.71 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.71 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.71 |
rpsA | 1834771 | c.1230G>A | synonymous_variant | 0.6 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.6 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.56 |
rpsA | 1834779 | p.Glu413Ala | missense_variant | 0.56 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.56 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.59 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.53 |
rpsA | 1834813 | c.1272G>C | synonymous_variant | 0.5 |
rpsA | 1834831 | c.1290G>C | synonymous_variant | 0.36 |
rpsA | 1834837 | p.Met432Ile | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918530 | c.591G>T | synonymous_variant | 0.2 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155225 | p.Met296Lys | missense_variant | 0.17 |
katG | 2155547 | p.Asp189Asn | missense_variant | 0.25 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.2 |
katG | 2155655 | p.Lys153Gln | missense_variant | 0.25 |
katG | 2155661 | p.Val151Ile | missense_variant | 0.25 |
katG | 2155674 | c.438G>A | synonymous_variant | 0.54 |
katG | 2155680 | c.432G>A | synonymous_variant | 0.67 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.64 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.69 |
katG | 2155719 | c.393G>C | synonymous_variant | 0.69 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.67 |
katG | 2155742 | p.Gly124Arg | missense_variant | 0.67 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.67 |
katG | 2155747 | p.Ala122Gly | missense_variant | 0.67 |
katG | 2155752 | c.360C>T | synonymous_variant | 0.67 |
katG | 2155758 | c.354C>T | synonymous_variant | 0.67 |
katG | 2155764 | p.His116Glu | missense_variant | 0.67 |
katG | 2155769 | p.Ile115Val | missense_variant | 0.57 |
katG | 2155770 | c.342C>G | synonymous_variant | 0.57 |
katG | 2155782 | c.330C>G | synonymous_variant | 0.62 |
katG | 2155785 | p.Ala109Ser | missense_variant | 0.62 |
katG | 2155796 | p.Ala106Ser | missense_variant | 0.62 |
katG | 2155806 | c.306T>C | synonymous_variant | 0.53 |
katG | 2155821 | c.291C>T | synonymous_variant | 0.27 |
katG | 2155828 | p.Tyr95Phe | missense_variant | 0.22 |
katG | 2155833 | c.279C>T | synonymous_variant | 0.22 |
PPE35 | 2167687 | p.Asn976Tyr | missense_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.56 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.44 |
kasA | 2517959 | c.-156C>T | upstream_gene_variant | 0.36 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.4 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.29 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.25 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518727 | p.Leu205Val | missense_variant | 0.25 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726418 | p.Glu76Lys | missense_variant | 1.0 |
ahpC | 2726449 | p.Ser86Leu | missense_variant | 0.22 |
ahpC | 2726561 | c.369T>C | synonymous_variant | 0.25 |
ahpC | 2726564 | c.372C>T | synonymous_variant | 0.25 |
ahpC | 2726567 | c.375C>G | synonymous_variant | 0.25 |
ahpC | 2726582 | c.390G>C | synonymous_variant | 0.2 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.22 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.22 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.43 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.4 |
ahpC | 2726615 | c.423C>T | synonymous_variant | 0.4 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.39 |
ahpC | 2726651 | c.459G>C | synonymous_variant | 0.37 |
ahpC | 2726654 | c.462G>C | synonymous_variant | 0.37 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.37 |
ahpC | 2726663 | c.471C>T | synonymous_variant | 0.37 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.37 |
ahpC | 2726676 | c.484C>T | synonymous_variant | 0.39 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.39 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.37 |
ahpC | 2726714 | c.522C>T | synonymous_variant | 0.29 |
ahpC | 2726717 | c.525A>C | synonymous_variant | 0.29 |
folC | 2746234 | p.Asp455Glu | missense_variant | 0.2 |
folC | 2747048 | p.Thr184Ser | missense_variant | 0.17 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.15 |
thyA | 3073874 | p.Ile200Val | missense_variant | 0.15 |
thyA | 3073878 | p.Glu198Asp | missense_variant | 0.17 |
thyA | 3073881 | c.591C>T | synonymous_variant | 0.18 |
thyA | 3073888 | p.Ser195Glu | missense_variant | 0.18 |
thyA | 3073890 | c.580_582delTTGinsCTC | synonymous_variant | 0.18 |
thyA | 3073903 | p.Ala190Asp | missense_variant | 0.17 |
thyA | 3073905 | c.567C>G | synonymous_variant | 0.2 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.22 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.2 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.17 |
thyA | 3073934 | p.Ser180Cys | missense_variant | 0.17 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.2 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.4 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.38 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.37 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.38 |
thyA | 3074058 | c.414C>T | synonymous_variant | 0.38 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.38 |
thyA | 3074076 | c.396C>A | synonymous_variant | 0.42 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.43 |
thyA | 3074082 | c.390G>C | synonymous_variant | 0.42 |
thyA | 3074089 | p.Ile128Asn | missense_variant | 0.43 |
thyA | 3074094 | c.378G>A | synonymous_variant | 0.43 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.43 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.43 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.43 |
thyA | 3074110 | p.Thr121Ser | missense_variant | 0.45 |
thyA | 3074115 | c.357G>C | synonymous_variant | 0.45 |
thyA | 3074121 | p.Asp117Glu | missense_variant | 0.45 |
thyA | 3074124 | c.348G>C | synonymous_variant | 0.45 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.45 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.48 |
thyA | 3074135 | p.Ser113Gly | missense_variant | 0.48 |
thyA | 3074154 | c.318T>C | synonymous_variant | 0.55 |
thyA | 3074281 | p.Arg64His | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473846 | c.-161T>A | upstream_gene_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568427 | p.Arg85Cys | missense_variant | 0.67 |
whiB7 | 3568828 | c.-150delA | upstream_gene_variant | 0.25 |
alr | 3841246 | p.Ala59Ser | missense_variant | 0.18 |
rpoA | 3877569 | p.Pro313Ala | missense_variant | 0.27 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.37 |
rpoA | 3877596 | c.912G>C | synonymous_variant | 0.38 |
rpoA | 3877600 | p.Gln303Ala | missense_variant | 0.35 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.53 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.53 |
rpoA | 3877629 | c.879C>G | synonymous_variant | 0.5 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.55 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.58 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.61 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.64 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.67 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.67 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.67 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.78 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.82 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.81 |
rpoA | 3877740 | c.768G>C | synonymous_variant | 0.79 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.87 |
rpoA | 3877765 | p.Ala248Ser | missense_variant | 0.88 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.88 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.91 |
rpoA | 3877800 | c.708G>C | synonymous_variant | 0.87 |
rpoA | 3877827 | p.Val227Thr | missense_variant | 0.83 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.85 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 0.85 |
rpoA | 3877847 | c.661C>T | synonymous_variant | 0.79 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.81 |
rpoA | 3877860 | c.648C>G | synonymous_variant | 0.82 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.79 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.79 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 0.75 |
rpoA | 3877898 | p.Pro204Ala | missense_variant | 0.67 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.73 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.73 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.73 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.68 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.68 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.7 |
rpoA | 3877935 | p.Lys191Arg | missense_variant | 0.7 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.69 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.62 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.61 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.62 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 0.63 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.62 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.52 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.52 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.52 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.52 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.52 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.52 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.52 |
rpoA | 3878043 | c.465G>C | synonymous_variant | 0.52 |
rpoA | 3878046 | c.462T>A | synonymous_variant | 0.53 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.55 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.56 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.56 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.58 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.58 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.65 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.64 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.64 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.68 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.74 |
rpoA | 3878124 | c.384G>C | synonymous_variant | 0.72 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.75 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.75 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.74 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.84 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.85 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.81 |
rpoA | 3878185 | p.Gly108Ala | missense_variant | 0.83 |
rpoA | 3878188 | p.Ala107Gly | missense_variant | 0.8 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.8 |
rpoA | 3878196 | p.Glu104Thr | missense_variant | 0.8 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.78 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.77 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.65 |
rpoA | 3878251 | c.256_257delTCinsAG | synonymous_variant | 0.65 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.58 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.56 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.56 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.48 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.45 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.44 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.44 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.39 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.39 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.41 |
rpoA | 3878331 | c.177A>C | synonymous_variant | 0.39 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.37 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.37 |
rpoA | 3878519 | c.-12A>G | upstream_gene_variant | 0.29 |
ddn | 3986832 | c.-12A>T | upstream_gene_variant | 0.25 |
clpC1 | 4038421 | p.Arg762Cys | missense_variant | 0.2 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.53 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.59 |
clpC1 | 4038710 | c.1995G>A | synonymous_variant | 0.62 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.76 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.74 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.73 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.73 |
clpC1 | 4038779 | c.1924_1926delCTCinsTTG | synonymous_variant | 0.7 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.71 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.74 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.79 |
clpC1 | 4038810 | p.Gln632Ser | missense_variant | 0.81 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.81 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.81 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.82 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.82 |
clpC1 | 4038896 | c.1809C>G | synonymous_variant | 0.79 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.8 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.81 |
clpC1 | 4038914 | c.1791G>T | synonymous_variant | 0.81 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.81 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.81 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.81 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.82 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.85 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.82 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.83 |
clpC1 | 4038983 | c.1722C>T | synonymous_variant | 0.83 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.85 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.86 |
clpC1 | 4039009 | c.1696C>T | synonymous_variant | 0.88 |
clpC1 | 4039016 | c.1689C>G | synonymous_variant | 0.87 |
clpC1 | 4039021 | c.1684C>T | synonymous_variant | 0.88 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.88 |
clpC1 | 4039046 | c.1659C>A | synonymous_variant | 0.9 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.92 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.92 |
clpC1 | 4039082 | c.1623C>T | synonymous_variant | 0.91 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.91 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.94 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.93 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.97 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.98 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.97 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.95 |
clpC1 | 4039136 | c.1569C>T | synonymous_variant | 0.95 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.95 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.95 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.93 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.93 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.9 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.9 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.9 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.9 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.93 |
clpC1 | 4039223 | c.1482C>T | synonymous_variant | 0.81 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.75 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.65 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.64 |
clpC1 | 4039286 | p.Leu473Met | missense_variant | 0.64 |
clpC1 | 4039293 | c.1411_1412insTG | frameshift_variant | 0.59 |
clpC1 | 4039296 | c.1407_1408delTT | frameshift_variant | 0.59 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.5 |
clpC1 | 4039313 | c.1392C>T | synonymous_variant | 0.5 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.5 |
clpC1 | 4039322 | c.1383T>G | synonymous_variant | 0.48 |
clpC1 | 4039327 | p.Gln460Glu | missense_variant | 0.48 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.5 |
clpC1 | 4039334 | c.1371G>T | synonymous_variant | 0.5 |
clpC1 | 4039337 | c.1368A>C | synonymous_variant | 0.5 |
clpC1 | 4039340 | c.1365G>A | synonymous_variant | 0.5 |
clpC1 | 4039347 | p.Arg453Lys | missense_variant | 0.5 |
clpC1 | 4039352 | c.1353C>A | synonymous_variant | 0.46 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.5 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.57 |
clpC1 | 4039407 | p.Arg433Lys | missense_variant | 0.4 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.4 |
clpC1 | 4039412 | c.1293T>C | synonymous_variant | 0.43 |
clpC1 | 4039424 | p.Lys427Arg | missense_variant | 0.46 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.46 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.46 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.6 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.6 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.6 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.67 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.83 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.85 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.97 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.97 |
clpC1 | 4039552 | c.1153C>T | synonymous_variant | 0.96 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.89 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.89 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.89 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.86 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.86 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.86 |
clpC1 | 4039582 | p.Thr375Ser | missense_variant | 0.87 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.86 |
clpC1 | 4039601 | p.Ala368Ser | missense_variant | 0.82 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.81 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.82 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.74 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.79 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.78 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.8 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.8 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.82 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.82 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.81 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.75 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.74 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.75 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.75 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.73 |
clpC1 | 4039766 | c.939T>G | synonymous_variant | 0.75 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.73 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.73 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.7 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.73 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.73 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.72 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.67 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.65 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.65 |
clpC1 | 4039856 | c.849C>T | synonymous_variant | 0.68 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.69 |
clpC1 | 4039883 | c.822G>A | synonymous_variant | 0.63 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.7 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.64 |
clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.66 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.68 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.67 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.62 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.64 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.66 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.67 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.63 |
clpC1 | 4039996 | p.Glu237Lys | missense_variant | 0.65 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.64 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.65 |
clpC1 | 4040021 | c.684A>G | synonymous_variant | 0.66 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.67 |
clpC1 | 4040027 | c.678C>G | synonymous_variant | 0.67 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.67 |
clpC1 | 4040072 | c.633C>T | synonymous_variant | 0.66 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.62 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.61 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.61 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.52 |
clpC1 | 4040135 | c.570C>T | synonymous_variant | 0.48 |
clpC1 | 4040138 | c.567G>C | synonymous_variant | 0.43 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.38 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.43 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.43 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.42 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.42 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.42 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.42 |
clpC1 | 4040213 | p.Ser164Thr | missense_variant | 0.47 |
clpC1 | 4040225 | p.Gly160Ser | missense_variant | 0.5 |
clpC1 | 4040228 | p.Gly159Ser | missense_variant | 0.5 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.58 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.64 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.53 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.65 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.68 |
clpC1 | 4040300 | c.405C>T | synonymous_variant | 0.68 |
clpC1 | 4040306 | c.399G>A | synonymous_variant | 0.61 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.56 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.53 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.4 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.45 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.62 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.66 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.68 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.68 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.69 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.7 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.71 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.68 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.68 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.61 |
clpC1 | 4040432 | c.271_273delAGCinsTCG | synonymous_variant | 0.61 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.65 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.62 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.58 |
clpC1 | 4040453 | c.252C>A | synonymous_variant | 0.58 |
clpC1 | 4040456 | c.249C>G | synonymous_variant | 0.58 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.58 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.6 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.6 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.6 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.58 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.35 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.35 |
clpC1 | 4040531 | c.174T>G | synonymous_variant | 0.31 |
clpC1 | 4040539 | c.166C>T | synonymous_variant | 0.25 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.25 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.25 |
clpC1 | 4040549 | c.154_156delTTGinsCTC | synonymous_variant | 0.25 |
clpC1 | 4040555 | c.150G>A | synonymous_variant | 0.25 |
clpC1 | 4040558 | c.147G>C | synonymous_variant | 0.27 |
clpC1 | 4040561 | p.Ser48Ala | missense_variant | 0.27 |
clpC1 | 4040567 | c.138C>G | synonymous_variant | 0.27 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.27 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.29 |
clpC1 | 4040582 | c.123G>T | synonymous_variant | 0.29 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.29 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.25 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.25 |
clpC1 | 4040600 | c.103_105delTTAinsCTC | synonymous_variant | 0.29 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.29 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.29 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 1.0 |
embC | 4240411 | c.549G>C | synonymous_variant | 0.3 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244479 | p.Thr416Lys | missense_variant | 0.17 |
embA | 4244671 | p.Ala480Asp | missense_variant | 0.22 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247335 | c.822C>T | synonymous_variant | 0.25 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247711 | p.Asn400Tyr | missense_variant | 0.25 |
aftB | 4267079 | c.1758A>G | synonymous_variant | 0.4 |
aftB | 4267960 | p.Val293Met | missense_variant | 1.0 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.44 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethA | 4327126 | p.Trp116Cys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |