Run ID: ERR4820335
Sample name:
Date: 01-04-2023 16:37:28
Number of reads: 1995326
Percentage reads mapped: 80.5
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 | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.78 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.25 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.25 |
gyrA | 6376 | c.-926G>A | upstream_gene_variant | 0.18 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.16 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.16 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.15 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.16 |
gyrB | 7124 | p.Ser629Thr | missense_variant | 0.14 |
gyrA | 7129 | c.-173T>C | upstream_gene_variant | 0.14 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.14 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.24 |
gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.19 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.17 |
gyrA | 7186 | c.-116C>G | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.14 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.14 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.13 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.2 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.14 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.15 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.16 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.23 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.23 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.22 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.22 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.21 |
gyrA | 7562 | c.261C>T | synonymous_variant | 0.14 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.16 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.17 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.19 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.21 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.21 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.21 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.14 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.14 |
gyrA | 8780 | p.Asp493Glu | missense_variant | 0.12 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.2 |
gyrA | 8807 | c.1506C>T | synonymous_variant | 0.18 |
gyrA | 8810 | c.1509A>G | synonymous_variant | 0.2 |
gyrA | 8816 | c.1515C>G | synonymous_variant | 0.2 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.2 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.21 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.24 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.26 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.22 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.23 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.23 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.24 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.23 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.24 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.19 |
gyrA | 8946 | c.1645T>C | synonymous_variant | 0.14 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.16 |
gyrA | 9104 | c.1803C>G | synonymous_variant | 0.14 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.15 |
gyrA | 9122 | c.1821C>A | synonymous_variant | 0.14 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.16 |
gyrA | 9153 | p.Thr618Glu | missense_variant | 0.14 |
gyrA | 9158 | c.1857C>T | synonymous_variant | 0.16 |
gyrA | 9161 | c.1860C>G | synonymous_variant | 0.14 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 0.13 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.91 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.12 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.96 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.13 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.2 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.21 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.21 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.2 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.16 |
mshA | 575917 | p.Asp190Glu | missense_variant | 0.17 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.16 |
mshA | 575924 | p.Gly193Ser | missense_variant | 0.16 |
ccsA | 619699 | c.-192G>C | upstream_gene_variant | 0.13 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.14 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.86 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.14 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.14 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.14 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.13 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.14 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.17 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.17 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.13 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.13 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.17 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.17 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.18 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.15 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.17 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.13 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.15 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.17 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.17 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.16 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.14 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.13 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.14 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.24 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.31 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.24 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.23 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.18 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.17 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.15 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.15 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.19 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.16 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.2 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.25 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.23 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.26 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.2 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.27 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.17 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.18 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.13 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.13 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.16 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.17 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.18 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.18 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.21 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.13 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.15 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.14 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.13 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.14 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.14 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.15 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.15 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.36 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.37 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.35 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.23 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.19 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.19 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.14 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.14 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.14 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.14 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.14 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.14 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.19 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.15 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.14 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.18 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.16 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.12 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.17 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.19 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.21 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.15 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.13 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.12 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.14 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.28 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.42 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.21 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.26 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.19 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.17 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.18 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.15 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.13 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.14 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.17 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.18 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.12 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.12 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.13 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.15 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.13 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.14 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.14 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.97 |
rpoC | 765292 | c.1923G>C | synonymous_variant | 0.12 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.13 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.14 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.13 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.13 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.22 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.21 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.24 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.13 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.15 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.13 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.15 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.15 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.15 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.21 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.14 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.12 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.19 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.18 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.19 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.15 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.16 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.16 |
rpoC | 766030 | c.2661C>G | synonymous_variant | 0.15 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.16 |
rpoC | 766083 | p.Ala905Glu | missense_variant | 0.12 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.15 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.12 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.16 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.16 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.14 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.15 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.16 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.13 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.18 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.17 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.19 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.21 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.15 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.16 |
rpoC | 767009 | p.Ser1214Thr | missense_variant | 0.12 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.14 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.14 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.16 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.15 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.15 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.15 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.13 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.14 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.2 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.15 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.15 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.16 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.13 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.13 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.14 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.13 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.15 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.13 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.12 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.19 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.2 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.26 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.33 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.32 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.55 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.24 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.21 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.22 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.22 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.2 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.2 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.13 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.14 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.15 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474254 | n.597C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474774 | n.1117A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 0.14 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.15 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.15 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.17 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.16 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.16 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.2 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.17 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.17 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.17 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.2 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.18 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.16 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.17 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.13 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.14 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.15 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.13 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.2 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.18 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.17 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.17 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.15 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.14 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.14 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.14 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.14 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.17 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.15 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.14 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.16 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.15 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.18 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.19 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.18 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.27 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.26 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.18 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.17 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.17 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.16 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.13 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.15 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.15 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.24 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.24 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.23 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.21 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.2 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.21 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.16 |
Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 0.17 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.13 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.14 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.13 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.13 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.13 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.12 |
thyX | 3067691 | p.Ile85Met | missense_variant | 0.14 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.13 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.16 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.14 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.13 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.2 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.23 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.22 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.23 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.21 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.22 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.18 |
thyX | 3067935 | p.Thr4Ile | missense_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.15 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.15 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.14 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.13 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.16 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640612 | p.Gly24Ser | missense_variant | 1.0 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.15 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.14 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.14 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.16 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.14 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.16 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.15 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.12 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.13 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.14 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.14 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.14 |
ddn | 3987001 | p.Gly53Asp | missense_variant | 1.0 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.13 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.13 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.14 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.15 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.16 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.14 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.16 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.14 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.15 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.21 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.17 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.18 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 0.15 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.15 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.15 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.12 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.16 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.16 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.15 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.13 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.13 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.13 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.13 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.13 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.15 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.15 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.85 |
embA | 4242820 | c.-413G>C | upstream_gene_variant | 0.15 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.15 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.16 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.15 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.16 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.13 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.14 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.17 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.16 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.16 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.16 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.15 |
embB | 4248373 | c.1860C>G | synonymous_variant | 0.14 |
embB | 4248386 | c.1873C>A | synonymous_variant | 0.15 |
embB | 4248407 | p.Leu632Val | missense_variant | 0.13 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.19 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |