Run ID: SRR7496471
Sample name:
Date: 04-04-2023 19:08:01
Number of reads: 318767
Percentage reads mapped: 23.13
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5627 | p.Ala130Thr | missense_variant | 0.25 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.89 |
gyrB | 6130 | c.891T>C | synonymous_variant | 0.43 |
gyrB | 6151 | c.912C>T | synonymous_variant | 0.43 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.6 |
gyrB | 6196 | c.957C>T | synonymous_variant | 0.6 |
gyrB | 6737 | p.Thr500Ala | missense_variant | 0.2 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.2 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.2 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 0.2 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.22 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.29 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.29 |
gyrA | 6805 | c.-497G>C | upstream_gene_variant | 0.55 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.5 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.75 |
gyrA | 6850 | c.-452C>A | upstream_gene_variant | 0.6 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.6 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.6 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.6 |
gyrA | 6866 | c.-436C>T | upstream_gene_variant | 0.6 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.6 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.6 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.6 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.6 |
gyrA | 6898 | c.-404G>A | upstream_gene_variant | 0.5 |
gyrB | 6911 | p.Asn558His | missense_variant | 0.67 |
gyrA | 6916 | c.-386G>C | upstream_gene_variant | 0.67 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.67 |
gyrA | 6922 | c.-380G>C | upstream_gene_variant | 0.67 |
gyrB | 6924 | p.Phe562Tyr | missense_variant | 0.67 |
gyrA | 6926 | c.-376_-374delTTGinsCTA | upstream_gene_variant | 0.67 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.67 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.67 |
gyrB | 7044 | p.Asn602Ser | missense_variant | 0.5 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.5 |
gyrA | 7081 | c.-221T>C | upstream_gene_variant | 0.5 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.5 |
gyrB | 7088 | p.Asp617Asn | missense_variant | 0.5 |
gyrA | 7093 | c.-209T>C | upstream_gene_variant | 0.5 |
gyrA | 7100 | c.-202T>C | upstream_gene_variant | 0.75 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.86 |
gyrB | 7124 | p.Ser629Glu | missense_variant | 0.86 |
gyrA | 7132 | c.-170T>C | upstream_gene_variant | 0.86 |
gyrA | 7136 | c.-166T>C | upstream_gene_variant | 0.86 |
gyrA | 7141 | c.-161T>G | upstream_gene_variant | 1.0 |
gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
gyrA | 7150 | c.-152G>C | upstream_gene_variant | 1.0 |
gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
gyrA | 7165 | c.-137C>T | upstream_gene_variant | 1.0 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
gyrA | 7177 | c.-125G>A | upstream_gene_variant | 0.67 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.67 |
gyrA | 7198 | c.-104C>T | upstream_gene_variant | 0.33 |
gyrA | 7207 | c.-95C>T | upstream_gene_variant | 0.33 |
gyrB | 7209 | p.Asp657Ala | missense_variant | 0.33 |
gyrA | 7213 | c.-89G>C | upstream_gene_variant | 0.33 |
gyrA | 7216 | c.-86G>C | upstream_gene_variant | 0.33 |
gyrA | 7225 | c.-77T>C | upstream_gene_variant | 0.33 |
gyrB | 7229 | p.Thr664Ala | missense_variant | 0.33 |
gyrA | 7234 | c.-68C>T | upstream_gene_variant | 0.33 |
gyrA | 7240 | c.-62C>G | upstream_gene_variant | 0.25 |
gyrA | 7243 | c.-59G>A | upstream_gene_variant | 0.25 |
gyrA | 7252 | c.-50G>C | upstream_gene_variant | 0.25 |
gyrA | 7258 | c.-44G>T | upstream_gene_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.18 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.2 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8231 | c.932dupG | frameshift_variant | 0.29 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.18 |
gyrA | 8829 | c.1528_1530delTTGinsCTC | synonymous_variant | 0.29 |
gyrA | 8849 | c.1548C>G | synonymous_variant | 0.47 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.55 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.52 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.52 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.52 |
gyrA | 8876 | c.1575C>T | synonymous_variant | 0.54 |
gyrA | 8913 | p.Lys538Arg | missense_variant | 0.65 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.65 |
gyrA | 8930 | c.1629C>T | synonymous_variant | 0.62 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.65 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.65 |
gyrA | 8945 | c.1644G>T | synonymous_variant | 0.65 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.65 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.68 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.6 |
gyrA | 8982 | p.Cys561Ser | missense_variant | 0.6 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.58 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.58 |
gyrA | 9002 | c.1701C>T | synonymous_variant | 0.58 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.58 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.5 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.5 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.5 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.5 |
gyrA | 9038 | c.1737C>G | synonymous_variant | 0.5 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.5 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 0.47 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.47 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.47 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.47 |
gyrA | 9063 | p.Ser588Asn | missense_variant | 0.47 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.5 |
gyrA | 9074 | c.1773G>T | synonymous_variant | 0.5 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 0.4 |
gyrA | 9113 | c.1812C>G | synonymous_variant | 0.36 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.36 |
gyrA | 9128 | c.1827C>G | synonymous_variant | 0.22 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 576367 | c.1020T>C | synonymous_variant | 0.5 |
mshA | 576685 | c.1338C>G | synonymous_variant | 0.4 |
rpoB | 760070 | c.264T>C | synonymous_variant | 0.59 |
rpoB | 760091 | c.285G>T | synonymous_variant | 0.58 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.58 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.56 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.58 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.56 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.56 |
rpoB | 760120 | p.Arg105His | missense_variant | 0.56 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.55 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.6 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.6 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.59 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.62 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.65 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.67 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.67 |
rpoB | 760185 | c.379C>T | synonymous_variant | 0.73 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.68 |
rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 0.68 |
rpoB | 760241 | c.435G>C | synonymous_variant | 0.67 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.66 |
rpoB | 760265 | p.Met153Ile | missense_variant | 0.68 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.66 |
rpoB | 760282 | p.Thr159Ser | missense_variant | 0.66 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.62 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.48 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.43 |
rpoB | 760330 | c.525_526delGT | frameshift_variant | 0.37 |
rpoB | 760340 | c.534_535insC | frameshift_variant | 0.37 |
rpoB | 760343 | c.537G>C | synonymous_variant | 0.39 |
rpoB | 760354 | p.Glu183Ala | missense_variant | 0.37 |
rpoB | 760356 | p.Thr184Ala | missense_variant | 0.37 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.4 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.48 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.52 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.58 |
rpoB | 760390 | p.Ser195Thr | missense_variant | 0.62 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.63 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.67 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.69 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.71 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.75 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.74 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.74 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.57 |
rpoB | 760515 | p.Trp237Leu | missense_variant | 0.57 |
rpoB | 760522 | p.Ser239Thr | missense_variant | 0.57 |
rpoB | 760527 | p.Gln241Glu | missense_variant | 0.57 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.59 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.59 |
rpoB | 760541 | c.735G>A | synonymous_variant | 0.59 |
rpoB | 760547 | c.741G>T | synonymous_variant | 0.59 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.58 |
rpoB | 760568 | c.762G>C | synonymous_variant | 0.58 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.58 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.62 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.5 |
rpoB | 760616 | p.Asp270Glu | missense_variant | 0.5 |
rpoB | 760617 | p.Ile271Val | missense_variant | 0.5 |
rpoB | 760640 | c.834C>T | synonymous_variant | 0.5 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.45 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.4 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.33 |
rpoB | 760669 | p.Thr288Asn | missense_variant | 0.2 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.2 |
rpoB | 760682 | c.876C>T | synonymous_variant | 0.2 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.44 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.44 |
rpoB | 760871 | c.1065C>G | synonymous_variant | 0.47 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 0.5 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.5 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.5 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.62 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.67 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.7 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.7 |
rpoB | 760961 | c.1155C>G | synonymous_variant | 0.71 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.71 |
rpoB | 760973 | c.1167G>T | synonymous_variant | 0.76 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 0.76 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.86 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.86 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.83 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.83 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.92 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.93 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.93 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.93 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.93 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.93 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.93 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.93 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.93 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.88 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.89 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.93 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.93 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.92 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.92 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.92 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.92 |
rpoB | 761178 | c.1372_1374delTCAinsAGC | synonymous_variant | 0.9 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.91 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.84 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.84 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.79 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.79 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.79 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.74 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.71 |
rpoB | 761261 | c.1455G>A | synonymous_variant | 0.71 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.7 |
rpoB | 761276 | c.1470G>C | synonymous_variant | 0.76 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.75 |
rpoB | 761294 | c.1488G>C | synonymous_variant | 0.75 |
rpoB | 761309 | c.1503C>T | synonymous_variant | 0.71 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.69 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.78 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.78 |
rpoB | 761345 | c.1539G>T | synonymous_variant | 0.71 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.57 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.5 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.5 |
rpoB | 761367 | p.Glu521Gln | missense_variant | 0.5 |
rpoB | 761374 | p.Val523Glu | missense_variant | 0.5 |
rpoB | 761379 | p.Leu525Met | missense_variant | 0.4 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.29 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.29 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.25 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.25 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.25 |
rpoB | 761594 | c.1788C>G | synonymous_variant | 0.4 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.4 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.4 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.4 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.4 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.4 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.4 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.5 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.5 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.5 |
rpoB | 761650 | p.Ser615Asn | missense_variant | 0.5 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.5 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.5 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.5 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.33 |
rpoB | 761681 | c.1875G>A | synonymous_variant | 0.33 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.33 |
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 | 0.33 |
rpoB | 761711 | c.1905C>G | synonymous_variant | 0.33 |
rpoB | 761714 | c.1908C>G | synonymous_variant | 0.33 |
rpoB | 761718 | p.Ala638Ser | missense_variant | 0.33 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 0.33 |
rpoB | 761724 | p.Glu640Lys | missense_variant | 0.33 |
rpoB | 761728 | p.Ser641Thr | missense_variant | 0.33 |
rpoB | 761732 | c.1926C>T | synonymous_variant | 0.33 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.33 |
rpoB | 761736 | p.Ile644Val | missense_variant | 0.33 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.5 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.5 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.45 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.42 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.42 |
rpoB | 761789 | c.1983G>C | synonymous_variant | 0.42 |
rpoB | 761790 | p.Arg662Asp | missense_variant | 0.42 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.4 |
rpoB | 761816 | c.2010C>G | synonymous_variant | 0.4 |
rpoB | 761819 | c.2013G>T | synonymous_variant | 0.4 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.4 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.29 |
rpoB | 761863 | p.Ala686Glu | missense_variant | 0.31 |
rpoB | 761867 | c.2061C>T | synonymous_variant | 0.31 |
rpoB | 761868 | p.Asp688Gln | missense_variant | 0.31 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.27 |
rpoB | 761876 | c.2070C>G | synonymous_variant | 0.27 |
rpoB | 761880 | p.Ala692Ser | missense_variant | 0.27 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.27 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.27 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.27 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.27 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.29 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.29 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.29 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.29 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 0.29 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 0.29 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.33 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.41 |
rpoB | 761969 | p.Glu721Asp | missense_variant | 0.45 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 0.48 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.48 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 0.45 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.45 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.45 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.5 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.48 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.48 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.62 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.62 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.62 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.6 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.6 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.6 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.58 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.65 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.71 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.71 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.71 |
rpoB | 762170 | c.2364C>G | synonymous_variant | 0.76 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.8 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.8 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.79 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.73 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.73 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.73 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.72 |
rpoB | 762299 | c.2493G>C | synonymous_variant | 0.7 |
rpoB | 762305 | c.2499G>C | synonymous_variant | 0.67 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.53 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.62 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 0.62 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.5 |
rpoB | 762336 | p.Ile844Val | missense_variant | 0.38 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.38 |
rpoB | 762344 | c.2538G>C | synonymous_variant | 0.38 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.38 |
rpoB | 762348 | c.2542_2543delTCinsAG | synonymous_variant | 0.38 |
rpoB | 762356 | p.Glu850Asp | missense_variant | 0.38 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.38 |
rpoB | 762368 | p.Glu854Asp | missense_variant | 0.38 |
rpoB | 762369 | c.2563_2565delTTGinsCTC | synonymous_variant | 0.38 |
rpoB | 762372 | p.Pro856Ala | missense_variant | 0.38 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.38 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.33 |
rpoC | 762392 | c.-978G>C | upstream_gene_variant | 0.33 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.38 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.38 |
rpoC | 762407 | c.-963G>C | upstream_gene_variant | 0.5 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.5 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 0.5 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.5 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.5 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.5 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.6 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.67 |
rpoB | 762490 | p.Val895Ala | missense_variant | 0.67 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.8 |
rpoB | 762785 | p.Asp993Glu | missense_variant | 0.8 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.8 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.8 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.8 |
rpoC | 762812 | c.-558C>A | upstream_gene_variant | 0.8 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.8 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.57 |
rpoC | 762827 | c.-543G>A | upstream_gene_variant | 0.57 |
rpoC | 762830 | c.-540C>T | upstream_gene_variant | 0.57 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.57 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.79 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.79 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.79 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.86 |
rpoC | 762887 | c.-483G>T | upstream_gene_variant | 0.78 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.83 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.84 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.89 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.9 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.92 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.8 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.8 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.81 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.83 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.82 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.82 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.82 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.82 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.83 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.87 |
rpoC | 763130 | c.-240G>A | upstream_gene_variant | 0.83 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.83 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.6 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.56 |
rpoC | 763185 | c.-185_-183delCTCinsTTG | upstream_gene_variant | 0.33 |
rpoB | 763282 | p.Asn1159Ile | missense_variant | 0.22 |
rpoC | 763447 | c.78C>T | synonymous_variant | 0.5 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.8 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.86 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.89 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.85 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.88 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.82 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.85 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.87 |
rpoC | 763597 | c.228G>A | synonymous_variant | 0.87 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.86 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.79 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.77 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.81 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.81 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.78 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.78 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.76 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.74 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.74 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.74 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.74 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.74 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.7 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.7 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.7 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.7 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.73 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.58 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.55 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.55 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.55 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.67 |
rpoC | 763819 | c.450G>T | synonymous_variant | 0.5 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.4 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764153 | p.Gln262Lys | missense_variant | 0.25 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.25 |
rpoC | 764162 | p.Ile265Leu | missense_variant | 0.25 |
rpoC | 764169 | p.Asn267Thr | missense_variant | 0.33 |
rpoC | 764182 | c.813C>T | synonymous_variant | 0.45 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.64 |
rpoC | 764194 | p.Glu275Asp | missense_variant | 0.5 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.5 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.5 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.5 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.5 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.64 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.71 |
rpoC | 764242 | c.873C>T | synonymous_variant | 0.71 |
rpoC | 764245 | c.876C>G | synonymous_variant | 0.71 |
rpoC | 764254 | c.885G>A | synonymous_variant | 0.62 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.62 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.65 |
rpoC | 764266 | c.897T>G | synonymous_variant | 0.69 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.69 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.72 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.76 |
rpoC | 764290 | c.921C>T | synonymous_variant | 0.78 |
rpoC | 764297 | p.Met310Leu | missense_variant | 0.79 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.83 |
rpoC | 764329 | c.960C>T | synonymous_variant | 0.83 |
rpoC | 764341 | c.972G>T | synonymous_variant | 0.83 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.77 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.79 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.79 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.79 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.77 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.76 |
rpoC | 764396 | c.1027C>T | synonymous_variant | 0.68 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.71 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.71 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.65 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.65 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.65 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.68 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.62 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.67 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.67 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.68 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.69 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.75 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.78 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.76 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.77 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.8 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.8 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.81 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.81 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.91 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.81 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.8 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.81 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.75 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.74 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.74 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.75 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.75 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.75 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.74 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.8 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.83 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.89 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.91 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.9 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.9 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.9 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.9 |
rpoC | 764764 | p.His465Gln | missense_variant | 0.87 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.87 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.88 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.92 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.92 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.93 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.93 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.93 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.9 |
rpoC | 764872 | c.1503A>T | synonymous_variant | 0.9 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.9 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.84 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.84 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.83 |
rpoC | 764908 | c.1539G>A | synonymous_variant | 0.83 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.82 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.82 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.83 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.84 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.78 |
rpoC | 765004 | c.1635G>C | synonymous_variant | 0.69 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.69 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.69 |
rpoC | 765013 | c.1644C>T | synonymous_variant | 0.69 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.69 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.69 |
rpoC | 765034 | c.1665T>G | synonymous_variant | 0.67 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.69 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.69 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.69 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.69 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.69 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.71 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.7 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.7 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.7 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.7 |
rpoC | 765121 | c.1752G>C | synonymous_variant | 0.6 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.36 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.4 |
rpoC | 765874 | c.2505G>C | synonymous_variant | 0.36 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.36 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.36 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.36 |
rpoC | 765908 | p.Leu847Ala | missense_variant | 0.33 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.29 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.29 |
rpoC | 765940 | c.2571A>C | synonymous_variant | 0.29 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.29 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.29 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.29 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.29 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.29 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.29 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.25 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.25 |
rpoC | 766255 | c.2886G>C | synonymous_variant | 0.4 |
rpoC | 766258 | c.2889T>C | synonymous_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 | 0.71 |
rpoC | 766288 | c.2919C>T | synonymous_variant | 0.83 |
rpoC | 766298 | p.Thr977His | missense_variant | 0.88 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 0.7 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.7 |
rpoC | 766333 | c.2964G>C | synonymous_variant | 0.77 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.85 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.85 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.85 |
rpoC | 766361 | p.Val998Ile | missense_variant | 0.85 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.85 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 0.88 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.88 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.88 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.8 |
rpoC | 766402 | c.3033C>G | synonymous_variant | 0.8 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.82 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.82 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.81 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.76 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.76 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.76 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.75 |
rpoC | 766480 | c.3111C>T | synonymous_variant | 0.63 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.63 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.63 |
rpoC | 766488 | c.3120_3125delGCGTGG | disruptive_inframe_deletion | 0.63 |
rpoC | 766498 | c.3130_3131insGTGTCG | disruptive_inframe_insertion | 0.63 |
rpoC | 766510 | c.3141C>G | synonymous_variant | 0.62 |
rpoC | 766513 | p.Asp1048Glu | missense_variant | 0.62 |
rpoC | 766517 | p.Thr1050Ser | missense_variant | 0.62 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.68 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.68 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.68 |
rpoC | 766542 | p.Gly1058Asp | missense_variant | 0.68 |
rpoC | 766546 | p.Glu1059Asp | missense_variant | 0.73 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.73 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.68 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.68 |
rpoC | 766582 | c.3213C>T | synonymous_variant | 0.67 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.65 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.65 |
rpoC | 766598 | p.Tyr1077Ile | missense_variant | 0.67 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.8 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 0.8 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.78 |
rpoC | 766633 | c.3264G>C | synonymous_variant | 0.78 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.73 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.71 |
rpoC | 766654 | c.3285C>G | synonymous_variant | 0.71 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.71 |
rpoC | 766660 | c.3291G>T | synonymous_variant | 0.71 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.71 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.74 |
rpoC | 766684 | c.3315C>G | synonymous_variant | 0.73 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.67 |
rpoC | 766693 | c.3324C>T | synonymous_variant | 0.67 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.67 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.63 |
rpoC | 766718 | p.Asp1117Asn | missense_variant | 0.69 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.75 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.75 |
rpoC | 766742 | p.Gln1125Met | missense_variant | 0.82 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.82 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.82 |
rpoC | 766754 | p.Glu1129Gln | missense_variant | 0.82 |
rpoC | 766763 | p.Ile1132Val | missense_variant | 0.82 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.82 |
rpoC | 766775 | p.Arg1136Asn | missense_variant | 0.82 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.68 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.74 |
rpoC | 766835 | p.Val1156Thr | missense_variant | 0.58 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.58 |
rpoC | 766846 | c.3477C>G | synonymous_variant | 0.54 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 0.54 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.54 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.54 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.5 |
rpoC | 766877 | p.Ser1170His | missense_variant | 0.5 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.5 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.5 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.5 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.5 |
rpoC | 766903 | c.3534C>T | synonymous_variant | 0.5 |
rpoC | 766910 | p.Ile1181Val | missense_variant | 0.5 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.5 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.5 |
rpoC | 766921 | c.3552G>C | synonymous_variant | 0.5 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.5 |
rpoC | 766935 | p.Glu1189Ala | missense_variant | 0.5 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.55 |
rpoC | 766944 | p.Arg1192Gln | missense_variant | 0.55 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.55 |
rpoC | 766951 | c.3582G>C | synonymous_variant | 0.64 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.69 |
rpoC | 766969 | c.3600C>G | synonymous_variant | 0.77 |
rpoC | 766972 | c.3603G>A | synonymous_variant | 0.77 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.79 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.83 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.82 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.84 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.84 |
rpoC | 767023 | p.Asp1218Glu | missense_variant | 0.88 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.88 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.77 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.77 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.77 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.76 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.76 |
rpoC | 767087 | p.Cys1240Ser | missense_variant | 0.76 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.72 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.71 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.71 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.67 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.64 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.64 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.76 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.73 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.5 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.5 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.5 |
rpoC | 767203 | c.3834C>G | synonymous_variant | 0.4 |
rpoC | 767206 | c.3837C>T | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777323 | c.1158C>A | synonymous_variant | 0.67 |
mmpL5 | 777907 | p.Leu192Val | missense_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.25 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.25 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.36 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.36 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.47 |
rpsL | 781664 | c.105C>G | synonymous_variant | 0.47 |
rpsL | 781670 | c.111G>C | synonymous_variant | 0.62 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.68 |
rpsL | 781685 | c.126G>T | synonymous_variant | 0.68 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.65 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.65 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.65 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.65 |
rpsL | 781725 | p.Lys56Arg | missense_variant | 0.65 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.65 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.65 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.65 |
rpsL | 781737 | p.Gln60Ser | missense_variant | 0.65 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.68 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.65 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.65 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.6 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.61 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.5 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.5 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.48 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.48 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.48 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.48 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.39 |
rpsL | 781859 | c.300T>G | synonymous_variant | 0.39 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.39 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.39 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.39 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.41 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.38 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.27 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.2 |
rplC | 800610 | c.-199_-197delCTAinsTTG | upstream_gene_variant | 0.41 |
rplC | 800615 | c.-194G>C | upstream_gene_variant | 0.41 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.41 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.37 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 0.29 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.33 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.29 |
rplC | 800667 | c.-142T>A | upstream_gene_variant | 0.18 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.18 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.21 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.21 |
Rv1258c | 1406103 | p.Arg413Leu | missense_variant | 0.5 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 0.88 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471930 | n.85G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471931 | n.86G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472067 | n.222G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472445 | n.601dupT | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472463 | n.618G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472497 | n.652G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472841 | n.996G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472960 | n.1115G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472986 | n.1141C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1473694 | n.37C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473719 | n.62G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473732 | n.75G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473750 | n.93C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473811 | n.154C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473812 | n.155G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473815 | n.158T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473835 | n.179delA | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1473934 | n.277G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473935 | n.278C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473946 | n.289A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473968 | n.311C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474303 | n.646A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474306 | n.649A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474307 | n.650G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474310 | n.655dupG | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474356 | n.699T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474447 | n.790G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474448 | n.791T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474450 | n.793T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475059 | n.1404_1405delCA | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475064 | n.1407G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475067 | n.1410_1411insG | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475080 | n.1423G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475081 | n.1424C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475201 | n.1544G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475212 | n.1555A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475221 | n.1564C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475222 | n.1565G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475246 | n.1589C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475251 | n.1596_1599delTCCC | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475264 | n.1607G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475266 | n.1609T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475267 | n.1610G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475268 | n.1611T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475271 | n.1615_1618delGTTC | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475294 | n.1637T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475295 | n.1638C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475307 | n.1650T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475443 | n.1786G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475444 | n.1787G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475607 | n.1950A>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475609 | n.1952C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475614 | n.1957A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475627 | n.1970G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475628 | n.1971G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475633 | n.1976G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475636 | n.1979A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475769 | n.2113_2114insCG | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476029 | n.2373_2377delACCTC | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.89 |
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 | 0.92 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.56 |
rpsA | 1833586 | c.45C>T | synonymous_variant | 0.46 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.46 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.46 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.46 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.67 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.67 |
rpsA | 1833623 | p.Lys28Ser | missense_variant | 0.67 |
rpsA | 1833658 | c.117C>G | synonymous_variant | 0.63 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 0.68 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.67 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.67 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.7 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.7 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.71 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.71 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.71 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.68 |
rpsA | 1833739 | c.198C>T | synonymous_variant | 0.69 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.72 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 0.69 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.69 |
rpsA | 1833782 | p.Ser81Asn | missense_variant | 0.69 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.69 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.7 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.74 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.74 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.74 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.74 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.74 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.74 |
rpsA | 1833862 | c.321G>A | synonymous_variant | 0.73 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.76 |
rpsA | 1833877 | c.336C>T | synonymous_variant | 0.77 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.85 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.87 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.83 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.82 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.8 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.77 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.77 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.75 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.75 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.75 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.69 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.68 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.7 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.68 |
rpsA | 1834066 | c.525G>A | synonymous_variant | 0.57 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.54 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.56 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.56 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.56 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.6 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.58 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.62 |
rpsA | 1834157 | c.616_618delTTGinsCTC | synonymous_variant | 0.62 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.62 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.62 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 0.62 |
rpsA | 1834172 | c.631_632insGG | frameshift_variant | 0.62 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.68 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.74 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.7 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.65 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.67 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.6 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.58 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.6 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.64 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.64 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.65 |
rpsA | 1834282 | c.741C>T | synonymous_variant | 0.67 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.8 |
rpsA | 1834298 | p.Gln253Ala | missense_variant | 0.8 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.8 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.8 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.74 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.71 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.71 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.71 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.71 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.71 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.71 |
rpsA | 1834372 | c.831G>A | synonymous_variant | 0.71 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.67 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.68 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.7 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.67 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.7 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.65 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.67 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.68 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.68 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.68 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.64 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.7 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.7 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.69 |
rpsA | 1834522 | c.981C>T | synonymous_variant | 0.73 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.76 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.76 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.77 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.79 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.72 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.7 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.7 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.69 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.69 |
rpsA | 1834627 | c.1086C>T | synonymous_variant | 0.69 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.69 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.69 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.75 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.65 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.62 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.61 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 0.6 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.54 |
rpsA | 1834756 | c.1215G>A | synonymous_variant | 0.52 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.52 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.54 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.45 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.45 |
rpsA | 1834779 | p.Glu413Ala | missense_variant | 0.45 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.47 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.47 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.62 |
rpsA | 1834813 | c.1272G>C | synonymous_variant | 0.58 |
rpsA | 1834831 | c.1290G>T | synonymous_variant | 0.75 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169151 | p.Pro488Ser | missense_variant | 0.29 |
PPE35 | 2169874 | p.Ile247Phe | missense_variant | 0.2 |
PPE35 | 2170477 | p.Gly46Ser | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289170 | c.72C>T | synonymous_variant | 0.22 |
kasA | 2517953 | c.-162C>T | upstream_gene_variant | 0.41 |
kasA | 2517959 | c.-156C>T | upstream_gene_variant | 0.41 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.31 |
kasA | 2517968 | c.-147T>A | upstream_gene_variant | 0.27 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.27 |
kasA | 2517983 | c.-132T>C | upstream_gene_variant | 0.25 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2714780 | p.Gln185Lys | missense_variant | 0.25 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726579 | c.387T>G | synonymous_variant | 0.29 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.29 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.29 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.33 |
ahpC | 2726648 | c.456T>A | synonymous_variant | 0.33 |
ahpC | 2726654 | c.462G>C | synonymous_variant | 0.33 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.33 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.33 |
ahpC | 2726684 | c.492G>C | synonymous_variant | 0.22 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.22 |
folC | 2747223 | p.Glu126Lys | missense_variant | 0.67 |
ribD | 2986827 | c.-12G>T | upstream_gene_variant | 0.22 |
Rv2752c | 3065074 | c.1117delT | frameshift_variant | 0.2 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.5 |
thyA | 3073926 | c.546G>A | synonymous_variant | 0.5 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.5 |
thyA | 3073933 | c.538_539delAGinsTC | synonymous_variant | 0.5 |
thyA | 3073953 | c.519T>G | synonymous_variant | 0.5 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.5 |
thyA | 3073971 | c.501C>T | synonymous_variant | 0.5 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.5 |
thyA | 3073980 | c.492C>T | synonymous_variant | 0.5 |
thyA | 3073992 | c.478_480delAGCinsTCG | synonymous_variant | 0.5 |
thyA | 3073995 | c.477G>C | synonymous_variant | 0.5 |
thyA | 3073999 | p.Arg158Lys | missense_variant | 0.6 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.5 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.38 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.38 |
thyA | 3074046 | c.426G>A | synonymous_variant | 0.5 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.38 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.38 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.38 |
thyA | 3074070 | c.402C>T | synonymous_variant | 0.38 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087854 | c.1035G>A | synonymous_variant | 0.5 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474170 | p.Pro55Arg | missense_variant | 0.29 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474764 | p.Arg253Leu | missense_variant | 0.29 |
fprA | 3474930 | c.924C>T | synonymous_variant | 0.25 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiA | 3640506 | c.-37G>A | upstream_gene_variant | 0.33 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640672 | p.Val44Ile | missense_variant | 0.22 |
fbiB | 3640695 | c.-840C>G | upstream_gene_variant | 0.22 |
fbiA | 3640701 | p.Ile53Met | missense_variant | 0.22 |
fbiB | 3640707 | c.-828G>T | upstream_gene_variant | 0.22 |
fbiA | 3640708 | p.Leu56Val | missense_variant | 0.22 |
fbiA | 3640714 | p.Val58Ile | missense_variant | 0.22 |
fbiB | 3640722 | c.-813G>C | upstream_gene_variant | 0.22 |
fbiB | 3640728 | c.-807G>C | upstream_gene_variant | 0.22 |
fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 0.2 |
fbiA | 3640936 | p.Leu132Val | missense_variant | 0.25 |
fbiB | 3641772 | p.Asp80Asn | missense_variant | 0.25 |
rpoA | 3877569 | p.Pro313Ala | missense_variant | 0.17 |
rpoA | 3877587 | c.921A>C | synonymous_variant | 0.27 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.3 |
rpoA | 3877599 | p.Gln303Ala | missense_variant | 0.3 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.42 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.42 |
rpoA | 3877623 | c.885C>T | synonymous_variant | 0.5 |
rpoA | 3877629 | c.879C>G | synonymous_variant | 0.5 |
rpoA | 3877638 | c.870T>G | synonymous_variant | 0.62 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.67 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.77 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.77 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.77 |
rpoA | 3877674 | c.834C>G | synonymous_variant | 0.77 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.77 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.77 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.77 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.71 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.75 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.89 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.89 |
rpoA | 3877743 | p.Asp255Glu | missense_variant | 0.89 |
rpoA | 3877746 | c.762G>C | synonymous_variant | 0.89 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.9 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.9 |
rpoA | 3877765 | p.Ala248Ser | missense_variant | 0.84 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.84 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.84 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.84 |
rpoA | 3877803 | c.705G>T | synonymous_variant | 0.81 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.76 |
rpoA | 3877827 | c.681C>G | synonymous_variant | 0.76 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.86 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 0.83 |
rpoA | 3877845 | c.663G>C | synonymous_variant | 0.89 |
rpoA | 3877848 | c.660C>G | synonymous_variant | 0.89 |
rpoA | 3877854 | c.652_654delTTGinsCTC | synonymous_variant | 0.89 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.89 |
rpoA | 3877863 | c.645G>C | synonymous_variant | 0.89 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.89 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 1.0 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 1.0 |
rpoA | 3877898 | p.Pro204Ala | missense_variant | 1.0 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 1.0 |
rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
rpoA | 3877936 | p.Lys191Arg | missense_variant | 1.0 |
rpoA | 3877938 | c.570C>T | synonymous_variant | 1.0 |
rpoA | 3877959 | c.549C>G | synonymous_variant | 1.0 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.87 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.87 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.86 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.86 |
rpoA | 3878010 | c.498C>G | synonymous_variant | 0.85 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.85 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.73 |
rpoA | 3878025 | c.483C>G | synonymous_variant | 0.73 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.73 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.73 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.73 |
rpoA | 3878046 | c.462T>G | synonymous_variant | 0.75 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.75 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.75 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.78 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.81 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.82 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.83 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.83 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.83 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.79 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.83 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.84 |
rpoA | 3878142 | p.Gly122Asp | missense_variant | 0.83 |
rpoA | 3878185 | p.Gly108Ala | missense_variant | 0.81 |
rpoA | 3878188 | p.Ala107Gly | missense_variant | 0.82 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.82 |
rpoA | 3878196 | p.Glu104Thr | missense_variant | 0.82 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.82 |
rpoA | 3878214 | c.294C>T | synonymous_variant | 0.89 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.89 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.86 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.86 |
rpoA | 3878251 | c.256_257delTCinsAG | synonymous_variant | 0.86 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.86 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.89 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.88 |
rpoA | 3878276 | c.232C>T | synonymous_variant | 0.83 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.82 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.78 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.78 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.73 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.71 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.71 |
rpoA | 3878328 | c.180G>C | synonymous_variant | 0.67 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.63 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.59 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.5 |
rpoA | 3878357 | p.Val51Ile | missense_variant | 0.42 |
rpoA | 3878361 | c.147G>T | synonymous_variant | 0.42 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.36 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.36 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.36 |
rpoA | 3878376 | c.130_132delTCGinsAGC | synonymous_variant | 0.36 |
rpoA | 3878379 | c.129G>C | synonymous_variant | 0.36 |
rpoA | 3878388 | c.120C>T | synonymous_variant | 0.38 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.38 |
rpoA | 3878406 | c.102G>C | synonymous_variant | 0.45 |
rpoA | 3878421 | c.87A>C | synonymous_variant | 0.33 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.33 |
rpoA | 3878430 | c.78G>C | synonymous_variant | 0.25 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.29 |
rpoA | 3878450 | p.Gln20Lys | missense_variant | 0.29 |
rpoA | 3878544 | c.-37C>T | upstream_gene_variant | 1.0 |
ddn | 3986645 | c.-199G>A | upstream_gene_variant | 0.4 |
ddn | 3986656 | c.-188C>G | upstream_gene_variant | 0.4 |
ddn | 3986659 | c.-185_-184insCTC | upstream_gene_variant | 0.4 |
ddn | 3986672 | c.-172G>C | upstream_gene_variant | 0.4 |
ddn | 3986676 | c.-168_-166delATCinsGTG | upstream_gene_variant | 0.4 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.4 |
ddn | 3986703 | c.-141T>G | upstream_gene_variant | 0.4 |
ddn | 3987124 | p.Ala94Gly | missense_variant | 0.18 |
clpC1 | 4038377 | c.2328C>G | synonymous_variant | 0.33 |
clpC1 | 4038383 | c.2322G>T | synonymous_variant | 0.33 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.4 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.33 |
clpC1 | 4038395 | c.2310C>G | synonymous_variant | 0.33 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.33 |
clpC1 | 4038401 | c.2302_2304delTTGinsCTC | synonymous_variant | 0.4 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.5 |
clpC1 | 4038428 | c.2277G>C | synonymous_variant | 0.5 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.5 |
clpC1 | 4038444 | p.Ala754Arg | missense_variant | 0.5 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.5 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.5 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.38 |
clpC1 | 4038458 | c.2247G>C | synonymous_variant | 0.38 |
clpC1 | 4038461 | c.2244G>A | synonymous_variant | 0.38 |
clpC1 | 4038474 | p.Ser744Asn | missense_variant | 0.38 |
clpC1 | 4038479 | c.2226C>G | synonymous_variant | 0.38 |
clpC1 | 4038484 | c.2219_2220delGC | frameshift_variant | 0.29 |
clpC1 | 4038494 | c.2211G>T | synonymous_variant | 0.38 |
clpC1 | 4038498 | p.Ser736Asn | missense_variant | 0.44 |
clpC1 | 4038512 | c.2193C>T | synonymous_variant | 0.55 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.62 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.69 |
clpC1 | 4038536 | c.2169C>G | synonymous_variant | 0.72 |
clpC1 | 4038541 | c.2164C>T | synonymous_variant | 0.74 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.74 |
clpC1 | 4038559 | p.Ile716Val | missense_variant | 0.74 |
clpC1 | 4038584 | c.2121G>C | synonymous_variant | 0.72 |
clpC1 | 4038587 | c.2118C>T | synonymous_variant | 0.72 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.65 |
clpC1 | 4038604 | c.2101C>T | synonymous_variant | 0.64 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.64 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 0.67 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.67 |
clpC1 | 4038638 | c.2066dupA | frameshift_variant | 0.67 |
clpC1 | 4038648 | p.Gly686Asp | missense_variant | 0.67 |
clpC1 | 4038651 | p.Gly685Asp | missense_variant | 0.67 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.7 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.7 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.71 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.77 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.77 |
clpC1 | 4038698 | c.2007C>T | synonymous_variant | 0.77 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.77 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.77 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.77 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.77 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.8 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.89 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.88 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.88 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.87 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.86 |
clpC1 | 4038776 | c.1929G>A | synonymous_variant | 0.86 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.86 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.88 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.92 |
clpC1 | 4038810 | p.Gln632Ser | missense_variant | 0.82 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.8 |
clpC1 | 4038857 | c.1848C>T | synonymous_variant | 0.84 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.83 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.83 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.84 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.85 |
clpC1 | 4038905 | c.1800A>T | synonymous_variant | 0.85 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.84 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.84 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.84 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.85 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.85 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.85 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.85 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.85 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.86 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.86 |
clpC1 | 4038977 | c.1728G>A | synonymous_variant | 0.86 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.85 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.85 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.84 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.86 |
clpC1 | 4039019 | c.1686G>C | synonymous_variant | 0.8 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.79 |
clpC1 | 4039031 | c.1674T>A | synonymous_variant | 0.76 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.76 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.76 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.78 |
clpC1 | 4039088 | c.1617G>C | synonymous_variant | 0.78 |
clpC1 | 4039091 | c.1614G>A | synonymous_variant | 0.76 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.65 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.63 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.65 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.67 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.62 |
clpC1 | 4039136 | c.1569C>T | synonymous_variant | 0.58 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.54 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.54 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.5 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.5 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.5 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.5 |
clpC1 | 4039184 | c.1521G>A | synonymous_variant | 0.5 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.5 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.6 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.56 |
clpC1 | 4039244 | c.1461G>C | synonymous_variant | 0.56 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.67 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.67 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.67 |
clpC1 | 4039286 | p.Leu473Met | missense_variant | 0.67 |
clpC1 | 4039293 | c.1411_1412insTG | frameshift_variant | 0.67 |
clpC1 | 4039296 | c.1407_1408delTT | frameshift_variant | 0.67 |
clpC1 | 4039304 | c.1401G>A | synonymous_variant | 0.67 |
clpC1 | 4039313 | c.1392C>T | synonymous_variant | 0.67 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.67 |
clpC1 | 4039327 | p.Gln460Glu | missense_variant | 0.67 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.67 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.67 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.67 |
clpC1 | 4039340 | c.1365G>A | synonymous_variant | 0.67 |
clpC1 | 4039347 | p.Arg453Lys | missense_variant | 0.67 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.79 |
clpC1 | 4039355 | c.1350G>C | synonymous_variant | 0.79 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.8 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.92 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 1.0 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
clpC1 | 4039407 | p.Arg433Lys | missense_variant | 1.0 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
clpC1 | 4039412 | c.1293T>C | synonymous_variant | 1.0 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
clpC1 | 4039418 | c.1287C>T | synonymous_variant | 1.0 |
clpC1 | 4039424 | p.Lys427Arg | missense_variant | 1.0 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.91 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.93 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.88 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.87 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.8 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.8 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.67 |
clpC1 | 4039571 | c.1134G>C | synonymous_variant | 0.67 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.67 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.67 |
clpC1 | 4039583 | c.1122C>T | synonymous_variant | 0.8 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.8 |
clpC1 | 4039601 | p.Ala368Ser | missense_variant | 0.72 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.81 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.81 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.75 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.68 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.69 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.69 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.65 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.62 |
clpC1 | 4039694 | c.1011G>T | synonymous_variant | 0.62 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.63 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.68 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.68 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.7 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.76 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.74 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.76 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.76 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.77 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.77 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.77 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.74 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.74 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.74 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.74 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.71 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.76 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.74 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.71 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.75 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.78 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.76 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.76 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.76 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.76 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.74 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.81 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.8 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.8 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.78 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.72 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.81 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.73 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.68 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.68 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.68 |
clpC1 | 4040138 | c.567G>C | synonymous_variant | 0.2 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.4 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.25 |
clpC1 | 4040156 | p.Met183Gly | missense_variant | 0.25 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.29 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.29 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.29 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.29 |
clpC1 | 4040177 | c.528C>G | synonymous_variant | 0.29 |
clpC1 | 4040288 | c.417C>T | synonymous_variant | 0.22 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.22 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.22 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.22 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.22 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.22 |
clpC1 | 4040318 | c.387C>T | synonymous_variant | 0.22 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.22 |
clpC1 | 4040336 | c.369G>C | synonymous_variant | 0.22 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.3 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.27 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.27 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.25 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.2 |
clpC1 | 4040378 | c.325_327delTTGinsCTC | synonymous_variant | 0.2 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.2 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.21 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.21 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.21 |
clpC1 | 4040417 | c.286_288delCTGinsTTA | synonymous_variant | 0.21 |
clpC1 | 4040420 | c.285G>C | synonymous_variant | 0.21 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.21 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.21 |
clpC1 | 4040432 | c.271_273delAGCinsTCG | synonymous_variant | 0.21 |
clpC1 | 4040437 | c.268C>T | synonymous_variant | 0.21 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.31 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.31 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.31 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.31 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.36 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.36 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.4 |
clpC1 | 4040495 | c.210C>G | synonymous_variant | 0.36 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.67 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.33 |
clpC1 | 4040528 | c.177G>T | synonymous_variant | 0.33 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.33 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.33 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.2 |
clpC1 | 4040552 | c.153G>A | synonymous_variant | 0.2 |
clpC1 | 4040555 | c.150G>A | synonymous_variant | 0.2 |
clpC1 | 4040561 | p.Ser48Ala | missense_variant | 0.2 |
clpC1 | 4040573 | c.132T>G | synonymous_variant | 0.2 |
embC | 4240433 | p.Tyr191His | missense_variant | 0.29 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242067 | c.2205G>A | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244464 | p.Ala411Val | missense_variant | 0.25 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247260 | c.747C>T | synonymous_variant | 0.4 |
embB | 4247331 | p.Trp273Leu | missense_variant | 0.4 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267749 | p.Phe363Ser | missense_variant | 0.5 |
aftB | 4268125 | p.Ser238Gly | missense_variant | 0.4 |
aftB | 4268452 | c.384delG | frameshift_variant | 0.22 |
ubiA | 4269203 | p.Glu211Gln | missense_variant | 0.25 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.22 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.22 |
aftB | 4269231 | c.-395C>G | upstream_gene_variant | 0.22 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.22 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.2 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.2 |
aftB | 4269246 | c.-410G>C | upstream_gene_variant | 0.2 |
aftB | 4269264 | c.-428C>T | upstream_gene_variant | 0.2 |
aftB | 4269270 | c.-434G>A | upstream_gene_variant | 0.2 |
aftB | 4269291 | c.-455A>C | upstream_gene_variant | 0.25 |
ubiA | 4269297 | p.Ile179Val | missense_variant | 0.25 |
aftB | 4269305 | c.-469T>C | upstream_gene_variant | 0.25 |
aftB | 4269306 | c.-470T>C | upstream_gene_variant | 0.25 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4326437 | p.Leu346Pro | missense_variant | 0.22 |
ethA | 4327346 | p.Gly43Ala | missense_variant | 0.2 |
ethA | 4327451 | p.Val8Gly | missense_variant | 0.22 |
ethR | 4327741 | p.Phe65Ile | missense_variant | 0.33 |
whiB6 | 4338361 | p.Arg54Gln | 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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |