Run ID: ERR553132
Sample name:
Date: 15-08-2022 11:00:22
Number of reads: 1572604
Percentage reads mapped: 87.67
Strain: lineage4.1.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
La1.2.BCG | M.bovis | BCG | None | 0.05 |
lineage4.1 | Euro-American | T;X;H | None | 0.96 |
lineage4.1.2 | Euro-American | T;H | None | 0.97 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 0.83 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.83 | streptomycin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.15 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247580 | p.Ala356Val | missense_variant | 0.14 | ethambutol |
embB | 4247588 | p.Leu359Ile | missense_variant | 0.15 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.18 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.19 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.19 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.19 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.19 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.19 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.19 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.17 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.18 |
gyrA | 7090 | c.-212C>T | upstream_gene_variant | 0.16 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.15 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.16 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.95 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.96 |
rpoB | 760106 | c.300G>A | synonymous_variant | 0.92 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.92 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.16 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.15 |
rpoB | 760381 | p.Thr192Met | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.17 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.16 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.16 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.15 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.17 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.17 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.17 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.19 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.17 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.18 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.18 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.17 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.16 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.16 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.2 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.21 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.21 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.22 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.21 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.21 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.23 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.23 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.25 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.24 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.23 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.21 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.19 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.19 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.15 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.16 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.15 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.15 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.16 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.16 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.16 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.2 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.19 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.19 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.23 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.22 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.22 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.22 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.23 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.23 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.16 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.15 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.16 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.99 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.15 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.15 |
rpoC | 765329 | p.Ser654Gly | missense_variant | 0.15 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.16 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.16 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.18 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.2 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.23 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.22 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.2 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.21 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.21 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.22 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.24 |
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 | 0.18 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.19 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.18 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.17 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.17 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.17 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.16 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.16 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.15 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.13 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.14 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.14 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.15 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.14 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.15 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.15 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.15 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.15 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.15 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.13 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.24 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.25 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.24 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.23 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.21 |
rpoC | 766900 | c.3531T>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 | 0.21 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.2 |
rpoC | 766987 | c.3618G>C | synonymous_variant | 0.18 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.18 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.18 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.18 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.2 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.16 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.16 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.17 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.17 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.16 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.16 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.16 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.19 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.2 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.19 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.19 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.19 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.19 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473938 | n.281G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473939 | n.282C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473981 | n.324G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.23 |
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 | 0.25 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474091 | n.434C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474964 | n.1307T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.23 |
inhA | 1673685 | c.-517C>T | upstream_gene_variant | 0.16 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.16 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.15 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.14 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.14 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.14 |
rpsA | 1834333 | c.792C>T | synonymous_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.15 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.15 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.16 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.15 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.17 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.15 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.15 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.14 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.14 |
thyX | 3067531 | p.Ala139Thr | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.15 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.16 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.17 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.2 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.2 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.21 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.22 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.2 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.2 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.17 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.17 |
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 | 0.17 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.18 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.17 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.16 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.16 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.18 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.19 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.21 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.23 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.23 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.22 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.22 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.18 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.19 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.19 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.19 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.19 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.18 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.18 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.19 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.19 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.2 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.16 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.15 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.14 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.15 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.15 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.15 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.14 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.15 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.15 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.16 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.16 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.16 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.16 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.15 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.16 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.16 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.16 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.16 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.17 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.19 |
rpoA | 3878463 | c.45C>A | synonymous_variant | 0.14 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.14 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.14 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.16 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.16 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.16 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.16 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.16 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.17 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.18 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.17 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.17 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.16 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.15 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.16 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.16 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.16 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.19 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.18 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.18 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.18 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.18 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.19 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.19 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.21 |
clpC1 | 4038893 | c.1812C>T | synonymous_variant | 0.22 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.24 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.23 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.21 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.21 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.2 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.21 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.19 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.19 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.19 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.19 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.18 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.16 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.16 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.15 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.15 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.14 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.16 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.16 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.17 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.15 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.15 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.17 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.17 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.17 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.17 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.17 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.17 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.17 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.18 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.18 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.18 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.18 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.17 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.16 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.17 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.16 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.17 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.15 |
clpC1 | 4040215 | p.Ser164Thr | missense_variant | 0.14 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.15 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.19 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.18 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.17 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.17 |
clpC1 | 4040276 | c.427_429delTCCinsAGT | synonymous_variant | 0.17 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.17 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.17 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.15 |
embC | 4240660 | c.798C>G | synonymous_variant | 0.15 |
embC | 4240669 | c.807G>C | synonymous_variant | 0.15 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.15 |
embC | 4240693 | c.831T>G | synonymous_variant | 0.15 |
embC | 4240699 | c.837C>G | synonymous_variant | 0.15 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.16 |
embC | 4241551 | c.1689A>G | synonymous_variant | 0.15 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.18 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.17 |
embC | 4241578 | c.1716G>C | synonymous_variant | 0.17 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.2 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.2 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.17 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.18 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.18 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.18 |
embC | 4241635 | c.1773G>C | synonymous_variant | 0.16 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.16 |
embC | 4241648 | c.1786_1788delTTGinsCTC | synonymous_variant | 0.16 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.16 |
embC | 4241665 | c.1803G>C | synonymous_variant | 0.17 |
embC | 4241671 | c.1809T>C | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.95 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.97 |
embB | 4247566 | c.1053C>A | synonymous_variant | 0.14 |
embB | 4247587 | c.1074G>A | synonymous_variant | 0.15 |
embB | 4247603 | c.1090C>T | synonymous_variant | 0.17 |
embB | 4247611 | c.1098G>T | synonymous_variant | 0.17 |
embB | 4247614 | c.1101T>C | synonymous_variant | 0.17 |
embB | 4247629 | c.1116C>G | synonymous_variant | 0.14 |
embB | 4247632 | c.1119C>G | synonymous_variant | 0.14 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.15 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.15 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.15 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.15 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.15 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.15 |
embB | 4248172 | c.1659G>C | synonymous_variant | 0.15 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.14 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.14 |
embB | 4249606 | c.3093C>A | synonymous_variant | 0.14 |
embB | 4249624 | c.3111C>G | synonymous_variant | 0.14 |
embB | 4249657 | c.3144C>G | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |