Run ID: ERR9786515
Sample name:
Date: 02-04-2023 12:29:38
Number of reads: 704965
Percentage reads mapped: 82.34
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.98 |
lineage4.1 | Euro-American | T;X;H | None | 0.64 |
lineage4.1.2 | Euro-American | T;H | None | 0.65 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.69 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247580 | p.Ala356Val | missense_variant | 0.15 | ethambutol |
embB | 4247588 | p.Leu359Ile | missense_variant | 0.15 | ethambutol |
embB | 4247708 | p.Asn399Asp | missense_variant | 0.16 | ethambutol |
ethA | 4326016 | c.1457delC | frameshift_variant | 0.65 | ethionamide |
gid | 4408100 | c.102delG | frameshift_variant | 0.84 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6238 | c.999G>A | synonymous_variant | 0.16 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.17 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.18 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.18 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.18 |
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.18 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.19 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.18 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.18 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.19 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.18 |
gyrA | 6728 | c.-574C>T | upstream_gene_variant | 0.16 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.15 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.16 |
gyrA | 6881 | c.-421_-419delTTGinsCTC | upstream_gene_variant | 0.16 |
gyrA | 6889 | c.-413G>C | upstream_gene_variant | 0.16 |
gyrA | 6898 | c.-404G>C | upstream_gene_variant | 0.18 |
gyrA | 6901 | c.-401G>C | upstream_gene_variant | 0.18 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.18 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.18 |
gyrA | 6916 | c.-386G>C | upstream_gene_variant | 0.18 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.18 |
gyrA | 6925 | c.-377T>C | upstream_gene_variant | 0.2 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.21 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.21 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.22 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.2 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.21 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.21 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.23 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.22 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.25 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.24 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.27 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.19 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.19 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.19 |
gyrA | 7090 | c.-212C>T | upstream_gene_variant | 0.14 |
gyrA | 7114 | c.-188C>A | upstream_gene_variant | 0.15 |
gyrA | 7123 | c.-179C>A | upstream_gene_variant | 0.16 |
gyrB | 7124 | p.Ser629Thr | missense_variant | 0.16 |
gyrA | 7129 | c.-173T>C | upstream_gene_variant | 0.17 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.17 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.17 |
gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.16 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.17 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.16 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.15 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.16 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.16 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.16 |
gyrA | 7562 | c.261C>T | synonymous_variant | 0.18 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.66 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.16 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.16 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.16 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.16 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.17 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.16 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.17 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.16 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.16 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.16 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.17 |
gyrA | 8543 | c.1242C>G | synonymous_variant | 0.21 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.17 |
gyrA | 8553 | c.1252C>A | synonymous_variant | 0.19 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.18 |
gyrA | 8579 | p.Asp426Glu | missense_variant | 0.17 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.15 |
gyrA | 8627 | c.1326C>A | synonymous_variant | 0.14 |
gyrA | 8807 | c.1506C>T | synonymous_variant | 0.14 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.17 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.16 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.16 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.23 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.23 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.24 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.23 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.22 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.21 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.2 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.2 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.2 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.22 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.18 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.18 |
gyrA | 8987 | c.1686C>A | synonymous_variant | 0.2 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.2 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.17 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.17 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.15 |
gyrA | 9153 | p.Thr618Glu | missense_variant | 0.17 |
gyrA | 9158 | c.1857C>T | synonymous_variant | 0.17 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.19 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.19 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.17 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.62 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.17 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.17 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.17 |
fgd1 | 490887 | c.105G>A | synonymous_variant | 0.19 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.21 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.22 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.24 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.24 |
fgd1 | 490917 | c.135C>G | synonymous_variant | 0.24 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.24 |
fgd1 | 490929 | c.147C>G | synonymous_variant | 0.24 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.24 |
fgd1 | 490935 | c.153C>G | synonymous_variant | 0.24 |
fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.24 |
fgd1 | 490962 | c.180T>G | synonymous_variant | 0.19 |
fgd1 | 490974 | c.192T>C | synonymous_variant | 0.21 |
fgd1 | 490977 | c.195C>G | synonymous_variant | 0.21 |
fgd1 | 490980 | p.Asn66Lys | missense_variant | 0.21 |
fgd1 | 490984 | p.Leu68Ile | missense_variant | 0.21 |
fgd1 | 490987 | p.Leu69Thr | missense_variant | 0.22 |
fgd1 | 490998 | c.216T>C | synonymous_variant | 0.27 |
fgd1 | 491001 | c.219G>C | synonymous_variant | 0.27 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.29 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.3 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.48 |
fgd1 | 491049 | c.267T>C | synonymous_variant | 0.48 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.45 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.39 |
fgd1 | 491082 | c.300T>C | synonymous_variant | 0.41 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.41 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.39 |
fgd1 | 491094 | c.312C>G | synonymous_variant | 0.39 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.38 |
fgd1 | 491100 | c.318C>T | synonymous_variant | 0.38 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.36 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.36 |
fgd1 | 491130 | c.348C>G | synonymous_variant | 0.33 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.3 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.33 |
fgd1 | 491173 | c.391C>A | synonymous_variant | 0.3 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.32 |
fgd1 | 491184 | c.402A>G | synonymous_variant | 0.3 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.25 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.24 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.25 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.25 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.24 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.24 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.25 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.2 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.21 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.96 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.44 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.15 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.15 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.15 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.15 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.15 |
mshA | 575752 | c.405G>C | synonymous_variant | 0.16 |
mshA | 575755 | c.408G>A | synonymous_variant | 0.16 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.17 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.17 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.17 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.16 |
mshA | 575809 | c.462C>T | synonymous_variant | 0.2 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.21 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.19 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.19 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.19 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.19 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.19 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.23 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.23 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.18 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.17 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.55 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.17 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.21 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.21 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.21 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.16 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.16 |
rpoB | 760381 | p.Thr192Met | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.2 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.2 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.21 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.21 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.16 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.19 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.16 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.16 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.19 |
rpoB | 760949 | c.1143C>T | synonymous_variant | 0.18 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.18 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.18 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.18 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.22 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.23 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.21 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.24 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.26 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.25 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.34 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.32 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.32 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.32 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.39 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.38 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.38 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.33 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.29 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.27 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.28 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.29 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.32 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.27 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.26 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.22 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.22 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.21 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.22 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.25 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.21 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.18 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.18 |
rpoB | 761373 | p.Val523His | missense_variant | 0.17 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.18 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.18 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.16 |
rpoB | 761438 | c.1632G>C | synonymous_variant | 0.16 |
rpoB | 761439 | p.Asp545Asn | missense_variant | 0.16 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.16 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.16 |
rpoB | 761452 | p.Val549Asp | missense_variant | 0.15 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.16 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.2 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.2 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.22 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.22 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.17 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.16 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.24 |
rpoB | 761639 | c.1833G>A | synonymous_variant | 0.24 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.23 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.27 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.25 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.2 |
rpoB | 761720 | c.1914C>G | synonymous_variant | 0.17 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.17 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.18 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.17 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.17 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.19 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.2 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.19 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.19 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.15 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.16 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.15 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.23 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.26 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.26 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.24 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.22 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.27 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.21 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.15 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.23 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.23 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.26 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.29 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.3 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.3 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.32 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.31 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.28 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.3 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.31 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.34 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.33 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.32 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.34 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.32 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.25 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.21 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.21 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.21 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.23 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.18 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.17 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.25 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.26 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.26 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.24 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.24 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.23 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.22 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.22 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.22 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.16 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.18 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.24 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.24 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.25 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.25 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.25 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.27 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.25 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.22 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.22 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.22 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.23 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.23 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.22 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.23 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.22 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.17 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.21 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.23 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.2 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.2 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.22 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.22 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.17 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.17 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.21 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.22 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.21 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.19 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.2 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.29 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.24 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.23 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.2 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.2 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.2 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.22 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.21 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.21 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.21 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.22 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.22 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.22 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.21 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.64 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.16 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.21 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.2 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.23 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.22 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.21 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.21 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.21 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.19 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.19 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.19 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.26 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.2 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.16 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.18 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.17 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.17 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.17 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.21 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.19 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.19 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.24 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.24 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.19 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.19 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.18 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.32 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.27 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.27 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.26 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.25 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.23 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.23 |
rpoC | 766030 | c.2661C>G | synonymous_variant | 0.22 |
rpoC | 766036 | c.2667C>T | synonymous_variant | 0.21 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.21 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.18 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.16 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.21 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.2 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.19 |
rpoC | 766168 | c.2799C>T | synonymous_variant | 0.19 |
rpoC | 766174 | p.Asn935Lys | missense_variant | 0.19 |
rpoC | 766178 | p.Ile937Val | missense_variant | 0.19 |
rpoC | 766185 | p.Glu939Ala | missense_variant | 0.19 |
rpoC | 766189 | c.2820T>C | synonymous_variant | 0.21 |
rpoC | 766192 | c.2823T>C | synonymous_variant | 0.21 |
rpoC | 766193 | p.Gln942Glu | missense_variant | 0.21 |
rpoC | 766204 | c.2835C>T | synonymous_variant | 0.23 |
rpoC | 766207 | c.2838T>C | synonymous_variant | 0.23 |
rpoC | 766216 | c.2847T>C | synonymous_variant | 0.23 |
rpoC | 766219 | p.Asp950Glu | missense_variant | 0.23 |
rpoC | 766222 | c.2853T>C | synonymous_variant | 0.23 |
rpoC | 766226 | c.2857T>C | synonymous_variant | 0.23 |
rpoC | 766231 | c.2862T>G | synonymous_variant | 0.23 |
rpoC | 766234 | c.2865T>C | synonymous_variant | 0.25 |
rpoC | 766237 | c.2868T>C | synonymous_variant | 0.23 |
rpoC | 766240 | c.2871T>C | synonymous_variant | 0.23 |
rpoC | 766243 | c.2874C>G | synonymous_variant | 0.21 |
rpoC | 766258 | c.2889T>C | synonymous_variant | 0.26 |
rpoC | 766273 | c.2904T>C | synonymous_variant | 0.22 |
rpoC | 766274 | p.Ala969Thr | missense_variant | 0.22 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 0.23 |
rpoC | 766288 | c.2919C>G | synonymous_variant | 0.19 |
rpoC | 766303 | c.2934C>T | synonymous_variant | 0.15 |
rpoC | 766327 | c.2958C>A | synonymous_variant | 0.17 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.17 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.17 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.21 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.22 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.21 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.21 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.17 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.17 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.17 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.17 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.19 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.21 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.21 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.21 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.17 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.21 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.23 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.23 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.23 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.22 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.22 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.19 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.19 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.17 |
rpoC | 767033 | p.Ser1222Thr | missense_variant | 0.14 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.17 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.21 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.17 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.21 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.17 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.17 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.16 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776656 | p.Gly609Arg | missense_variant | 0.42 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.18 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.17 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.2 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.2 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.21 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.22 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.22 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.26 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.25 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.23 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.22 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.22 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.19 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.23 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.23 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.24 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.22 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.24 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.22 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.22 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.23 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.23 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.21 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.26 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.28 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.3 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.2 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.23 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.23 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.22 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.19 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.2 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.2 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.17 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.16 |
rplC | 800875 | p.Val23Ile | missense_variant | 0.16 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.18 |
rplC | 800892 | c.84G>C | synonymous_variant | 0.17 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.18 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.22 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.22 |
rplC | 801423 | c.615G>C | synonymous_variant | 0.18 |
rplC | 801426 | c.618C>G | synonymous_variant | 0.18 |
rplC | 801427 | p.Met207Val | missense_variant | 0.2 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.19 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.2 |
fbiC | 1303654 | c.724C>T | synonymous_variant | 0.16 |
fbiC | 1303659 | c.729T>C | synonymous_variant | 0.16 |
fbiC | 1303661 | p.Val244Ala | missense_variant | 0.16 |
fbiC | 1303663 | c.733C>T | synonymous_variant | 0.16 |
fbiC | 1303671 | c.741C>T | synonymous_variant | 0.15 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.17 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.19 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.22 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 0.25 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.25 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.23 |
fbiC | 1303731 | c.801A>C | synonymous_variant | 0.22 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 0.22 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.22 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.2 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.2 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.17 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.21 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 0.21 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.21 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.17 |
fbiC | 1303797 | c.867A>G | synonymous_variant | 0.18 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.19 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.19 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.19 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.19 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.22 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.23 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.18 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472045 | n.200T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474963 | n.1306G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476048 | n.2391G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476108 | n.2451T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.16 |
inhA | 1674114 | c.-88T>A | upstream_gene_variant | 0.18 |
inhA | 1674123 | c.-79T>C | upstream_gene_variant | 0.2 |
inhA | 1674126 | c.-76G>C | upstream_gene_variant | 0.21 |
inhA | 1674132 | c.-70T>C | upstream_gene_variant | 0.18 |
fabG1 | 1674136 | p.Ser233Ala | missense_variant | 0.19 |
inhA | 1674141 | c.-61T>C | upstream_gene_variant | 0.18 |
inhA | 1674352 | p.Thr51Ala | missense_variant | 0.14 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.15 |
inhA | 1674375 | c.174C>G | synonymous_variant | 0.15 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.17 |
inhA | 1674387 | c.186A>G | synonymous_variant | 0.17 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.2 |
inhA | 1674428 | p.Gly76Asp | missense_variant | 0.18 |
inhA | 1674438 | c.237C>G | synonymous_variant | 0.18 |
inhA | 1674440 | p.Glu80Ala | missense_variant | 0.18 |
inhA | 1674443 | p.Ala81Glu | missense_variant | 0.18 |
inhA | 1674450 | c.249G>C | synonymous_variant | 0.17 |
inhA | 1674452 | p.Ala84Asp | missense_variant | 0.17 |
inhA | 1674471 | c.270G>C | synonymous_variant | 0.33 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.36 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.36 |
inhA | 1674504 | c.303C>G | synonymous_variant | 0.5 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.44 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.38 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.33 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.3 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.27 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.33 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.33 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.36 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.4 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.4 |
inhA | 1674601 | p.Leu134Thr | missense_variant | 0.38 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.25 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.29 |
inhA | 1674672 | c.471C>G | synonymous_variant | 0.25 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.29 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.25 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.16 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.18 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.23 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.21 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.22 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.24 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.23 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.23 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.25 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.25 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.25 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.24 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.15 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.17 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.18 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.19 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.19 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.21 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.19 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.19 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.17 |
rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 0.18 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.21 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.2 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.23 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.22 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.24 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.25 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.25 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.3 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.29 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.25 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.2 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.23 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.23 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.21 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.22 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.22 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.25 |
rpsA | 1834684 | c.1143C>T | synonymous_variant | 0.27 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.26 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.31 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.31 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.31 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.33 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.27 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.29 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.29 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.28 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.25 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918389 | c.450G>C | synonymous_variant | 0.17 |
tlyA | 1918392 | c.453A>C | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.68 |
kasA | 2518146 | p.Phe11Tyr | missense_variant | 0.16 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.17 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.17 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.14 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.19 |
kasA | 2518693 | c.579C>G | synonymous_variant | 0.18 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.17 |
kasA | 2518699 | c.585C>T | synonymous_variant | 0.17 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.17 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.18 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.2 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.2 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.24 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.23 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.23 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.18 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.17 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 0.91 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.16 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.19 |
Rv2752c | 3065007 | c.1185G>C | synonymous_variant | 0.23 |
Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 0.21 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.25 |
Rv2752c | 3065028 | p.Val388Ile | missense_variant | 0.21 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.26 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.29 |
Rv2752c | 3065052 | c.1140G>A | synonymous_variant | 0.29 |
Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.3 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.24 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.25 |
Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 0.25 |
Rv2752c | 3065082 | c.1110G>C | synonymous_variant | 0.25 |
Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 0.25 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.24 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.21 |
Rv2752c | 3065451 | c.741G>A | synonymous_variant | 0.14 |
Rv2752c | 3065463 | c.729T>C | synonymous_variant | 0.16 |
Rv2752c | 3065520 | c.672G>C | synonymous_variant | 0.16 |
Rv2752c | 3065535 | c.657C>T | synonymous_variant | 0.15 |
Rv2752c | 3065544 | c.648C>T | synonymous_variant | 0.16 |
Rv2752c | 3065553 | c.639A>G | synonymous_variant | 0.16 |
Rv2752c | 3065562 | c.630T>C | synonymous_variant | 0.16 |
Rv2752c | 3065569 | p.Ile208His | missense_variant | 0.16 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.16 |
Rv2752c | 3065586 | c.606C>T | synonymous_variant | 0.16 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.16 |
Rv2752c | 3065598 | c.594G>T | synonymous_variant | 0.16 |
Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 0.15 |
Rv2752c | 3066315 | c.-124C>T | upstream_gene_variant | 0.15 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.17 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.17 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.24 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.24 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.25 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.26 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.26 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.26 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.23 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.21 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.21 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.19 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.2 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.2 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.24 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.24 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.21 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.21 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.21 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.26 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.26 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.25 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.26 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.26 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.28 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.28 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.28 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.29 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.26 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.22 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.22 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.19 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.14 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.15 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.17 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.16 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.17 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.17 |
thyA | 3074055 | p.Glu139Pro | missense_variant | 0.16 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.17 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.19 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.15 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.15 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.16 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.17 |
thyA | 3074440 | p.Val11Ala | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.58 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.63 |
fprA | 3474222 | c.216G>A | synonymous_variant | 0.16 |
fprA | 3474225 | c.219C>T | synonymous_variant | 0.16 |
fprA | 3474231 | c.225C>G | synonymous_variant | 0.16 |
fprA | 3474237 | c.231C>T | synonymous_variant | 0.16 |
fprA | 3474249 | c.243T>C | synonymous_variant | 0.17 |
fprA | 3474252 | c.246G>C | synonymous_variant | 0.17 |
fprA | 3474253 | p.Val83Ser | missense_variant | 0.17 |
fprA | 3474270 | c.264C>G | synonymous_variant | 0.15 |
fprA | 3474273 | c.267G>A | synonymous_variant | 0.15 |
fprA | 3474277 | p.Gly91Ser | missense_variant | 0.15 |
alr | 3840764 | c.657G>C | synonymous_variant | 0.3 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.18 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.19 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.23 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.23 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.23 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.23 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.24 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.17 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.17 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.21 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.18 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.19 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.17 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.21 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.21 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.21 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.18 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.18 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.2 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.19 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.2 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.2 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.19 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.19 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.19 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.19 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.16 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.29 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.32 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.3 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.3 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.23 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.23 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.27 |
rpoA | 3878043 | c.465G>A | synonymous_variant | 0.27 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.26 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.26 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.26 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.25 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.25 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.28 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.27 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.24 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.23 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.22 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.21 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.21 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.21 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.21 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.24 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.24 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.28 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.28 |
rpoA | 3878181 | c.327C>T | synonymous_variant | 0.28 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.26 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.26 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.28 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.29 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.3 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.33 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.33 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.37 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.36 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.38 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.37 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.38 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.38 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.38 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.35 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.35 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.38 |
rpoA | 3878340 | c.168C>T | synonymous_variant | 0.43 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.44 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.54 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.52 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.52 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.52 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.55 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.55 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.53 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.41 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.33 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.36 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.31 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.25 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.25 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.2 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.2 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.21 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.2 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.2 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.2 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.19 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.17 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.17 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.17 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.17 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.18 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.19 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.2 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.18 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.16 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.17 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.17 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.17 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.17 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.15 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.17 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.17 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.16 |
embC | 4240141 | c.279A>G | synonymous_variant | 0.17 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.16 |
embC | 4240867 | c.1005T>C | synonymous_variant | 0.17 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.16 |
embC | 4240873 | c.1011C>G | synonymous_variant | 0.16 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.16 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.16 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.15 |
embC | 4240898 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.15 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.15 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.18 |
embC | 4241032 | c.1170G>C | synonymous_variant | 0.16 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.19 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.21 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.24 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.26 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.26 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.26 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.25 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.26 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.25 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.24 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.22 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.22 |
embC | 4241218 | c.1356G>C | synonymous_variant | 0.18 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.15 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.14 |
embC | 4241521 | c.1659T>C | synonymous_variant | 0.16 |
embC | 4241530 | c.1668C>A | synonymous_variant | 0.16 |
embC | 4241539 | c.1677T>C | synonymous_variant | 0.17 |
embC | 4241551 | c.1689A>G | synonymous_variant | 0.17 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.17 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.18 |
embC | 4241578 | c.1716G>C | synonymous_variant | 0.18 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.18 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.18 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.18 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.2 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.2 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.19 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.15 |
embC | 4241650 | p.Leu596Phe | missense_variant | 0.15 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.55 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.2 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.2 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.2 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.21 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.2 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.21 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.24 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.25 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.25 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.31 |
embA | 4245248 | c.2016G>C | synonymous_variant | 0.17 |
embA | 4245257 | c.2025A>G | synonymous_variant | 0.17 |
embA | 4245263 | c.2031A>G | synonymous_variant | 0.18 |
embA | 4245282 | p.Ile684Val | missense_variant | 0.15 |
embA | 4245885 | p.Asp885Asn | missense_variant | 0.14 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.14 |
embA | 4245942 | p.Arg904Ser | missense_variant | 0.17 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.16 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.17 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.16 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.16 |
embB | 4247566 | c.1053C>A | synonymous_variant | 0.15 |
embB | 4247587 | c.1074G>A | synonymous_variant | 0.15 |
embB | 4247603 | c.1090C>T | synonymous_variant | 0.2 |
embB | 4247611 | c.1098G>T | synonymous_variant | 0.17 |
embB | 4247614 | c.1101T>C | synonymous_variant | 0.17 |
embB | 4247692 | c.1179C>G | synonymous_variant | 0.14 |
embB | 4247716 | c.1203C>T | synonymous_variant | 0.18 |
embB | 4247722 | c.1209G>C | synonymous_variant | 0.15 |
embB | 4247797 | c.1284C>G | synonymous_variant | 0.21 |
embB | 4247800 | c.1287A>T | synonymous_variant | 0.21 |
embB | 4247803 | c.1290G>C | synonymous_variant | 0.21 |
embB | 4247815 | c.1302C>G | synonymous_variant | 0.22 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.22 |
embB | 4247830 | c.1317A>C | synonymous_variant | 0.19 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.19 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.19 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.18 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.17 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.15 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.17 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.17 |
embB | 4249435 | c.2922G>A | synonymous_variant | 0.18 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.18 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.25 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.29 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.22 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.29 |
aftB | 4268336 | c.501C>T | synonymous_variant | 0.15 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.18 |
aftB | 4269206 | c.-370C>T | upstream_gene_variant | 0.17 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.19 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.19 |
aftB | 4269242 | c.-406C>T | upstream_gene_variant | 0.21 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.23 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.23 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.24 |
ubiA | 4269285 | p.Gly183Ala | missense_variant | 0.19 |
aftB | 4269291 | c.-455A>G | upstream_gene_variant | 0.19 |
aftB | 4269300 | c.-464G>C | upstream_gene_variant | 0.19 |
ubiA | 4269312 | p.Lys174Gln | missense_variant | 0.2 |
aftB | 4269315 | c.-479C>A | upstream_gene_variant | 0.2 |
ubiA | 4269329 | p.Lys169Glu | missense_variant | 0.21 |
aftB | 4269342 | c.-506G>C | upstream_gene_variant | 0.23 |
aftB | 4269363 | c.-527T>C | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407650 | p.Asp185Asn | missense_variant | 0.48 |