Run ID: SRR6832178
Sample name:
Date: 04-04-2023 17:16:33
Number of reads: 1584680
Percentage reads mapped: 76.13
Strain: lineage4.2.1.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.94 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.99 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.88 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
folC | 2747141 | p.Glu153Ala | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247448 | p.His312Arg | missense_variant | 0.2 | ethambutol |
embB | 4247663 | p.Tyr384Asn | missense_variant | 0.16 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5284 | c.45G>A | synonymous_variant | 0.24 |
gyrB | 5287 | c.48T>C | synonymous_variant | 0.26 |
gyrB | 5293 | c.54C>G | synonymous_variant | 0.3 |
gyrB | 5302 | c.63A>G | synonymous_variant | 0.29 |
gyrB | 5305 | c.66G>A | synonymous_variant | 0.3 |
gyrB | 5308 | c.69G>A | synonymous_variant | 0.3 |
gyrB | 5341 | c.102T>C | synonymous_variant | 0.28 |
gyrB | 5359 | c.120C>T | synonymous_variant | 0.25 |
gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 0.21 |
gyrB | 5377 | c.138T>C | synonymous_variant | 0.28 |
gyrB | 5422 | c.183T>C | synonymous_variant | 0.16 |
gyrB | 5425 | c.186A>G | synonymous_variant | 0.16 |
gyrB | 5426 | p.Thr63Ala | missense_variant | 0.15 |
gyrB | 5431 | c.192A>C | synonymous_variant | 0.16 |
gyrB | 5434 | c.195G>A | synonymous_variant | 0.16 |
gyrB | 5436 | p.Asn66Ser | missense_variant | 0.15 |
gyrB | 5440 | c.201A>G | synonymous_variant | 0.16 |
gyrB | 5470 | c.231C>G | synonymous_variant | 0.13 |
gyrB | 5767 | c.528C>T | synonymous_variant | 0.17 |
gyrB | 5771 | p.Ala178Asn | missense_variant | 0.19 |
gyrB | 5779 | c.540C>T | synonymous_variant | 0.18 |
gyrB | 5782 | c.543A>G | synonymous_variant | 0.18 |
gyrB | 5788 | c.549G>C | synonymous_variant | 0.18 |
gyrB | 5791 | c.552A>G | synonymous_variant | 0.17 |
gyrB | 5812 | c.573C>A | synonymous_variant | 0.21 |
gyrB | 5815 | c.576C>A | synonymous_variant | 0.21 |
gyrB | 5819 | c.580C>T | synonymous_variant | 0.21 |
gyrB | 5824 | c.585A>G | synonymous_variant | 0.21 |
gyrB | 5836 | c.597C>T | synonymous_variant | 0.26 |
gyrB | 5851 | c.612G>C | synonymous_variant | 0.22 |
gyrB | 5860 | c.621C>T | synonymous_variant | 0.2 |
gyrB | 6079 | c.840C>T | synonymous_variant | 0.16 |
gyrB | 6085 | c.846C>A | synonymous_variant | 0.16 |
gyrB | 6086 | p.Thr283Pro | missense_variant | 0.17 |
gyrB | 6091 | c.852G>C | synonymous_variant | 0.18 |
gyrB | 6097 | c.858G>A | synonymous_variant | 0.18 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.23 |
gyrB | 6121 | c.882C>T | synonymous_variant | 0.21 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.21 |
gyrB | 6145 | c.906C>T | synonymous_variant | 0.23 |
gyrB | 6178 | c.939C>T | synonymous_variant | 0.2 |
gyrB | 6181 | c.942C>G | synonymous_variant | 0.2 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.17 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.22 |
gyrB | 6247 | c.1008G>A | synonymous_variant | 0.21 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.21 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.22 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.16 |
gyrA | 6991 | c.-311C>T | upstream_gene_variant | 0.15 |
gyrA | 6994 | c.-308C>T | upstream_gene_variant | 0.16 |
gyrA | 6997 | c.-305G>A | upstream_gene_variant | 0.15 |
gyrA | 7000 | c.-302C>T | upstream_gene_variant | 0.14 |
gyrA | 7006 | c.-296T>G | upstream_gene_variant | 0.15 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.19 |
gyrA | 7024 | c.-278G>C | upstream_gene_variant | 0.22 |
gyrA | 7030 | c.-272C>A | upstream_gene_variant | 0.2 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.19 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 0.22 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.21 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.16 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.17 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.17 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.2 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.29 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.26 |
gyrA | 7619 | c.318C>T | synonymous_variant | 0.23 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.23 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.21 |
gyrA | 7652 | c.351C>G | synonymous_variant | 0.2 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.14 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.31 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.31 |
gyrA | 7838 | c.537C>T | synonymous_variant | 0.33 |
gyrA | 7850 | c.549C>G | synonymous_variant | 0.31 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.29 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.24 |
gyrA | 7889 | c.588G>A | synonymous_variant | 0.24 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.22 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.15 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.17 |
gyrA | 8258 | c.957G>A | synonymous_variant | 0.18 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.17 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.18 |
gyrA | 8282 | c.981G>A | synonymous_variant | 0.15 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.15 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.15 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.17 |
gyrA | 8315 | c.1014G>A | synonymous_variant | 0.17 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.15 |
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.16 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.14 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.14 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.15 |
gyrA | 8531 | c.1230G>A | synonymous_variant | 0.19 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.19 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.14 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.14 |
gyrA | 8655 | p.Ile452Val | missense_variant | 0.15 |
gyrA | 8666 | c.1365G>C | synonymous_variant | 0.15 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.16 |
gyrA | 8723 | c.1422G>A | synonymous_variant | 0.26 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.29 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.29 |
gyrA | 8752 | p.Ala484Gly | missense_variant | 0.21 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.21 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.19 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.21 |
gyrA | 8783 | c.1482G>T | synonymous_variant | 0.19 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.19 |
gyrA | 8795 | c.1494C>T | synonymous_variant | 0.2 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.21 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.21 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.22 |
gyrA | 8813 | c.1512C>T | synonymous_variant | 0.23 |
gyrA | 8825 | c.1524G>A | synonymous_variant | 0.16 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.19 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.19 |
gyrA | 8924 | c.1623C>G | synonymous_variant | 0.19 |
gyrA | 8933 | c.1632G>A | synonymous_variant | 0.19 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.2 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.2 |
gyrA | 8945 | c.1644G>T | synonymous_variant | 0.19 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.19 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.2 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.19 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.18 |
gyrA | 9003 | c.1702C>T | synonymous_variant | 0.18 |
gyrA | 9017 | c.1716C>T | synonymous_variant | 0.18 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.19 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.18 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.18 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.16 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.15 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.14 |
gyrA | 9080 | c.1779G>C | synonymous_variant | 0.14 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.14 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.14 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.17 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.18 |
gyrA | 9257 | c.1956C>T | synonymous_variant | 0.18 |
gyrA | 9284 | c.1983T>G | synonymous_variant | 0.2 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9585 | c.2284T>C | synonymous_variant | 0.16 |
gyrA | 9626 | c.2325T>C | synonymous_variant | 0.16 |
gyrA | 9629 | c.2328C>A | synonymous_variant | 0.16 |
gyrA | 9630 | p.Val777Ile | missense_variant | 0.17 |
gyrA | 9635 | c.2334T>C | synonymous_variant | 0.18 |
gyrA | 9644 | c.2343T>C | synonymous_variant | 0.2 |
gyrA | 9650 | c.2349G>C | synonymous_variant | 0.21 |
gyrA | 9656 | c.2355C>G | synonymous_variant | 0.23 |
gyrA | 9659 | c.2358C>G | synonymous_variant | 0.24 |
gyrA | 9668 | c.2367C>A | synonymous_variant | 0.21 |
gyrA | 9689 | c.2388G>C | synonymous_variant | 0.21 |
gyrA | 9704 | c.2403T>C | synonymous_variant | 0.2 |
gyrA | 9707 | c.2406G>C | synonymous_variant | 0.21 |
gyrA | 9716 | c.2415T>C | synonymous_variant | 0.2 |
fgd1 | 490809 | c.27A>G | synonymous_variant | 0.19 |
fgd1 | 490818 | c.36C>T | synonymous_variant | 0.24 |
fgd1 | 490830 | c.48A>C | synonymous_variant | 0.26 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.3 |
fgd1 | 490853 | p.Ala24Gly | missense_variant | 0.3 |
fgd1 | 490863 | c.81C>A | synonymous_variant | 0.28 |
fgd1 | 490869 | c.87C>T | synonymous_variant | 0.3 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.29 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.3 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.21 |
fgd1 | 490911 | c.129T>C | synonymous_variant | 0.18 |
fgd1 | 490921 | p.Gln47Lys | missense_variant | 0.16 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.16 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.19 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.19 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.18 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.16 |
fgd1 | 491067 | c.285C>T | synonymous_variant | 0.17 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.2 |
fgd1 | 491085 | c.303T>G | synonymous_variant | 0.2 |
fgd1 | 491496 | c.714C>T | synonymous_variant | 0.15 |
fgd1 | 491499 | c.717G>C | synonymous_variant | 0.17 |
fgd1 | 491508 | c.726A>T | synonymous_variant | 0.14 |
fgd1 | 491523 | c.741G>A | synonymous_variant | 0.18 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.17 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.18 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.19 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.19 |
fgd1 | 491553 | c.771G>A | synonymous_variant | 0.19 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.24 |
fgd1 | 491604 | c.822G>C | synonymous_variant | 0.24 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.23 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.23 |
fgd1 | 491628 | c.846G>A | synonymous_variant | 0.18 |
fgd1 | 491643 | c.861G>C | synonymous_variant | 0.18 |
fgd1 | 491646 | c.864G>C | synonymous_variant | 0.18 |
fgd1 | 491664 | c.882C>G | synonymous_variant | 0.14 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.16 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.21 |
mshA | 575732 | c.385_387delCTTinsTTG | synonymous_variant | 0.18 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.17 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.17 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.19 |
mshA | 575770 | c.423G>C | synonymous_variant | 0.19 |
mshA | 575772 | p.Val142Ala | missense_variant | 0.18 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.19 |
mshA | 576166 | c.819C>G | synonymous_variant | 0.13 |
mshA | 576193 | c.846T>C | synonymous_variant | 0.14 |
mshA | 576202 | c.855T>C | synonymous_variant | 0.16 |
mshA | 576205 | c.858G>C | synonymous_variant | 0.16 |
mshA | 576207 | p.Ala287Val | missense_variant | 0.17 |
mshA | 576215 | c.868_870delTTGinsCTC | synonymous_variant | 0.17 |
mshA | 576220 | c.873C>G | synonymous_variant | 0.17 |
mshA | 576223 | c.876G>A | synonymous_variant | 0.17 |
mshA | 576230 | p.Ile295Val | missense_variant | 0.17 |
mshA | 576233 | p.Ile296Val | missense_variant | 0.15 |
mshA | 576238 | c.891G>C | synonymous_variant | 0.17 |
mshA | 576247 | c.900A>G | synonymous_variant | 0.17 |
ccsA | 620245 | p.Leu119Met | missense_variant | 0.18 |
ccsA | 620256 | c.366C>G | synonymous_variant | 0.14 |
ccsA | 620257 | p.Ile123Val | missense_variant | 0.15 |
ccsA | 620271 | c.381C>G | synonymous_variant | 0.14 |
ccsA | 620325 | c.435G>T | synonymous_variant | 0.15 |
ccsA | 620397 | c.507C>G | synonymous_variant | 0.16 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.16 |
ccsA | 620418 | c.528G>C | synonymous_variant | 0.16 |
ccsA | 620622 | c.732G>C | synonymous_variant | 0.15 |
ccsA | 620631 | c.741T>G | synonymous_variant | 0.15 |
ccsA | 620685 | c.795G>A | synonymous_variant | 0.16 |
rpoB | 759635 | c.-172C>T | upstream_gene_variant | 0.25 |
rpoB | 759644 | c.-163T>A | upstream_gene_variant | 0.26 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.27 |
rpoB | 759661 | c.-146G>C | upstream_gene_variant | 0.27 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.14 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.14 |
rpoB | 760193 | c.387C>G | synonymous_variant | 0.17 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.18 |
rpoB | 760202 | c.396G>A | synonymous_variant | 0.18 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.21 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.25 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.25 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.19 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.15 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.16 |
rpoB | 760343 | c.537G>C | synonymous_variant | 0.15 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.24 |
rpoB | 760409 | c.603C>T | synonymous_variant | 0.22 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.21 |
rpoB | 760415 | c.609C>G | synonymous_variant | 0.2 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.21 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.2 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.19 |
rpoB | 760445 | c.639C>T | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.2 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.15 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.17 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.16 |
rpoB | 760664 | c.858G>C | synonymous_variant | 0.15 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.14 |
rpoB | 760673 | c.867G>A | synonymous_variant | 0.15 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.15 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.17 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.17 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.19 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.21 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.21 |
rpoB | 760859 | c.1053T>G | synonymous_variant | 0.19 |
rpoB | 760868 | c.1062C>G | synonymous_variant | 0.2 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.17 |
rpoB | 760920 | c.1114C>T | synonymous_variant | 0.16 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.15 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.17 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.26 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.35 |
rpoB | 761036 | c.1230G>A | synonymous_variant | 0.34 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.34 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.4 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.4 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.28 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.28 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.15 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.15 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.24 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.25 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.24 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.25 |
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 | 0.24 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.19 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.14 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.22 |
rpoB | 761346 | p.Val514Ile | missense_variant | 0.19 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.17 |
rpoB | 761355 | p.Val517Leu | missense_variant | 0.17 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.18 |
rpoB | 761366 | c.1560C>T | synonymous_variant | 0.17 |
rpoB | 761373 | p.Val523His | missense_variant | 0.18 |
rpoB | 761379 | c.1573C>T | synonymous_variant | 0.18 |
rpoB | 761384 | c.1578C>G | synonymous_variant | 0.17 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.16 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.15 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.16 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.2 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.2 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.18 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.18 |
rpoB | 761600 | c.1794T>G | synonymous_variant | 0.2 |
rpoB | 761603 | c.1797C>T | synonymous_variant | 0.21 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.2 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.19 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.21 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.19 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.19 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.2 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.18 |
rpoB | 762020 | c.2214G>A | synonymous_variant | 0.18 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.18 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.26 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.22 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.27 |
rpoB | 762071 | c.2265C>T | synonymous_variant | 0.27 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.2 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.23 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.24 |
rpoB | 762119 | c.2313C>T | synonymous_variant | 0.23 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.22 |
rpoB | 762134 | c.2328C>G | synonymous_variant | 0.22 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.19 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.21 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.14 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.15 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.17 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.2 |
rpoC | 762518 | c.-852C>G | upstream_gene_variant | 0.27 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.27 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.32 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.32 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.29 |
rpoC | 762557 | c.-813G>C | upstream_gene_variant | 0.24 |
rpoC | 762581 | c.-789T>C | upstream_gene_variant | 0.17 |
rpoC | 762582 | c.-788T>C | upstream_gene_variant | 0.17 |
rpoC | 762587 | c.-783G>A | upstream_gene_variant | 0.17 |
rpoC | 762599 | c.-771T>A | upstream_gene_variant | 0.2 |
rpoC | 762605 | c.-765T>C | upstream_gene_variant | 0.16 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.15 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.24 |
rpoC | 762860 | c.-510G>T | upstream_gene_variant | 0.23 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.19 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.17 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.16 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.15 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoC | 763076 | c.-294C>T | upstream_gene_variant | 0.21 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.24 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.16 |
rpoC | 763408 | c.39T>C | synonymous_variant | 0.2 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.19 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.19 |
rpoC | 763430 | c.61A>C | synonymous_variant | 0.22 |
rpoC | 763435 | c.66A>G | synonymous_variant | 0.23 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.26 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.31 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.35 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.38 |
rpoC | 763505 | c.136C>T | synonymous_variant | 0.35 |
rpoC | 763561 | c.192G>A | synonymous_variant | 0.28 |
rpoC | 763600 | c.231C>T | synonymous_variant | 0.32 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.32 |
rpoC | 763618 | c.249C>A | synonymous_variant | 0.28 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.3 |
rpoC | 763636 | c.267T>G | synonymous_variant | 0.29 |
rpoC | 763639 | c.270G>A | synonymous_variant | 0.25 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.23 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.24 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.14 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.14 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.14 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.3 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.27 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.25 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.24 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.25 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.2 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.17 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.19 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.24 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.31 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.29 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.27 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.26 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.21 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.17 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.17 |
rpoC | 764272 | c.903G>T | synonymous_variant | 0.17 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.17 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.18 |
rpoC | 764404 | c.1035C>A | synonymous_variant | 0.13 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.13 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.23 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764648 | c.1279C>A | synonymous_variant | 0.21 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.21 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.2 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.18 |
rpoC | 764674 | c.1305G>A | synonymous_variant | 0.18 |
rpoC | 764681 | c.1312C>T | synonymous_variant | 0.2 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.29 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.26 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.24 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764767 | c.1398G>C | synonymous_variant | 0.24 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.2 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.18 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.17 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.17 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.19 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.17 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.15 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.19 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.19 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.24 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.24 |
rpoC | 764918 | p.Val517Ile | missense_variant | 0.2 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.2 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.2 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.2 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.22 |
rpoC | 765395 | c.2026C>T | synonymous_variant | 0.31 |
rpoC | 765405 | p.Leu679Pro | missense_variant | 0.27 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.23 |
rpoC | 765430 | c.2061G>A | synonymous_variant | 0.29 |
rpoC | 765445 | c.2076G>T | synonymous_variant | 0.24 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.23 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.23 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.21 |
rpoC | 765496 | c.2127C>G | synonymous_variant | 0.16 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.17 |
rpoC | 765526 | c.2157C>G | synonymous_variant | 0.16 |
rpoC | 765541 | c.2172C>A | synonymous_variant | 0.17 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.19 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.17 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.18 |
rpoC | 765688 | c.2319G>C | synonymous_variant | 0.17 |
rpoC | 765689 | c.2320C>T | synonymous_variant | 0.17 |
rpoC | 765694 | c.2325G>C | synonymous_variant | 0.17 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.17 |
rpoC | 765724 | c.2355C>G | synonymous_variant | 0.29 |
rpoC | 765727 | c.2358T>C | synonymous_variant | 0.31 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.21 |
rpoC | 765748 | c.2379C>T | synonymous_variant | 0.18 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.18 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.17 |
rpoC | 765826 | c.2457T>A | synonymous_variant | 0.26 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.26 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.31 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.36 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.38 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.35 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.33 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.38 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.37 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.33 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.31 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.33 |
rpoC | 765997 | c.2628T>C | synonymous_variant | 0.35 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.18 |
rpoC | 766300 | c.2931C>G | synonymous_variant | 0.15 |
rpoC | 766306 | c.2937C>T | synonymous_variant | 0.15 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.17 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.16 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.14 |
rpoC | 766360 | c.2991C>T | synonymous_variant | 0.15 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.24 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.24 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.25 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.26 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.27 |
rpoC | 766519 | c.3150C>A | synonymous_variant | 0.26 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.19 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.17 |
rpoC | 766537 | c.3168G>A | synonymous_variant | 0.17 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.17 |
rpoC | 766549 | c.3180G>T | synonymous_variant | 0.15 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.17 |
rpoC | 766681 | c.3312C>T | synonymous_variant | 0.18 |
rpoC | 766684 | c.3315C>G | synonymous_variant | 0.19 |
rpoC | 766700 | c.3331C>T | synonymous_variant | 0.24 |
rpoC | 766714 | c.3345G>C | synonymous_variant | 0.22 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.21 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.26 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.29 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.27 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.2 |
rpoC | 766795 | c.3426C>T | synonymous_variant | 0.2 |
rpoC | 766801 | c.3432C>T | synonymous_variant | 0.22 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.17 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.18 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.15 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.15 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.15 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.15 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.17 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.2 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.21 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.21 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.23 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.2 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.28 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.26 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.26 |
rpoC | 767185 | c.3816G>T | synonymous_variant | 0.26 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.25 |
rpoC | 767200 | c.3831G>A | synonymous_variant | 0.24 |
rpoC | 767206 | c.3837C>A | synonymous_variant | 0.22 |
rpoC | 767209 | c.3840T>G | synonymous_variant | 0.2 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.17 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.19 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776802 | p.Met560Thr | missense_variant | 1.0 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781586 | c.27C>A | synonymous_variant | 0.14 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.14 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.18 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.17 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.16 |
rpsL | 781667 | c.108C>G | synonymous_variant | 0.16 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.2 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.2 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.2 |
rpsL | 781721 | c.162C>G | synonymous_variant | 0.21 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.22 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.19 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.18 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.18 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.19 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.19 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.16 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.23 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.17 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.2 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.2 |
rplC | 800744 | c.-65G>C | upstream_gene_variant | 0.21 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.19 |
rplC | 800783 | c.-26C>T | upstream_gene_variant | 0.15 |
rplC | 800797 | c.-12T>G | upstream_gene_variant | 0.15 |
rplC | 800817 | c.9A>C | synonymous_variant | 0.19 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.15 |
rplC | 801339 | c.531T>G | synonymous_variant | 0.15 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.15 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.15 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.15 |
fbiC | 1303494 | p.Leu188Phe | missense_variant | 0.15 |
fbiC | 1303503 | c.573G>C | synonymous_variant | 0.16 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.14 |
fbiC | 1303512 | c.582T>G | synonymous_variant | 0.16 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.17 |
fbiC | 1303551 | c.621G>C | synonymous_variant | 0.17 |
fbiC | 1303578 | c.648G>A | synonymous_variant | 0.2 |
fbiC | 1303584 | c.654C>A | synonymous_variant | 0.2 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.15 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.16 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.18 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.16 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.2 |
fbiC | 1303683 | p.Leu251Phe | missense_variant | 0.16 |
fbiC | 1303689 | c.759T>C | synonymous_variant | 0.16 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.15 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.15 |
fbiC | 1303732 | p.Ser268Thr | missense_variant | 0.15 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.16 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.16 |
fbiC | 1303768 | p.Ser280Ala | missense_variant | 0.19 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.16 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.21 |
fbiC | 1304055 | p.Asp375Glu | missense_variant | 0.22 |
fbiC | 1304058 | p.Glu376Asp | missense_variant | 0.21 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.21 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.21 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.21 |
fbiC | 1304074 | p.Ala382Ser | missense_variant | 0.2 |
fbiC | 1304079 | c.1149A>G | synonymous_variant | 0.21 |
fbiC | 1304091 | c.1161C>T | synonymous_variant | 0.21 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.21 |
fbiC | 1304112 | c.1182G>A | synonymous_variant | 0.24 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.17 |
fbiC | 1304163 | c.1233G>C | synonymous_variant | 0.28 |
fbiC | 1304164 | p.Gly412Arg | missense_variant | 0.28 |
fbiC | 1304172 | c.1242G>T | synonymous_variant | 0.29 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.29 |
fbiC | 1304178 | c.1248G>C | synonymous_variant | 0.29 |
fbiC | 1304181 | c.1251G>T | synonymous_variant | 0.29 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.29 |
fbiC | 1304200 | p.Leu424Phe | missense_variant | 0.21 |
fbiC | 1304205 | c.1275C>G | synonymous_variant | 0.19 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.2 |
fbiC | 1304556 | c.1626C>T | synonymous_variant | 0.14 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.17 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.21 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.2 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.17 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.2 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.24 |
fbiC | 1304649 | c.1719C>T | synonymous_variant | 0.22 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.19 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.19 |
fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.19 |
fbiC | 1304679 | c.1749G>A | synonymous_variant | 0.19 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.19 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.2 |
fbiC | 1304703 | c.1773C>T | synonymous_variant | 0.18 |
fbiC | 1304715 | c.1785G>T | synonymous_variant | 0.23 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 0.18 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.18 |
fbiC | 1304790 | c.1860C>A | synonymous_variant | 0.18 |
fbiC | 1304799 | c.1869G>C | synonymous_variant | 0.19 |
fbiC | 1304925 | c.1995G>C | synonymous_variant | 0.15 |
fbiC | 1304934 | c.2004C>G | synonymous_variant | 0.15 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.17 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.17 |
fbiC | 1304943 | c.2013C>T | synonymous_variant | 0.2 |
fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.21 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.23 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.14 |
fbiC | 1305126 | c.2196T>C | synonymous_variant | 0.16 |
Rv1258c | 1406553 | p.Ala263Val | missense_variant | 0.14 |
Rv1258c | 1406556 | p.Trp262Ser | missense_variant | 0.14 |
Rv1258c | 1407254 | c.87G>A | synonymous_variant | 0.14 |
embR | 1416997 | c.351C>T | synonymous_variant | 0.14 |
atpE | 1461101 | c.57T>C | synonymous_variant | 0.21 |
atpE | 1461107 | c.63C>G | synonymous_variant | 0.2 |
atpE | 1461131 | c.87T>C | synonymous_variant | 0.16 |
atpE | 1461185 | c.141G>A | synonymous_variant | 0.14 |
atpE | 1461197 | c.153A>C | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471984 | n.139T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473541 | n.-117G>A | upstream_gene_variant | 0.14 |
rrl | 1473571 | n.-87C>T | upstream_gene_variant | 0.21 |
rrl | 1473592 | n.-66_-65insA | upstream_gene_variant | 0.18 |
rrl | 1473600 | n.-58A>G | upstream_gene_variant | 0.19 |
rrl | 1473603 | n.-55C>T | upstream_gene_variant | 0.24 |
rrl | 1473607 | n.-50_-49delGG | upstream_gene_variant | 0.18 |
rrl | 1473613 | n.-45G>C | upstream_gene_variant | 0.17 |
rrl | 1473614 | n.-44C>G | upstream_gene_variant | 0.17 |
rrl | 1473618 | n.-40G>A | upstream_gene_variant | 0.17 |
rrl | 1473626 | n.-32_-31insT | upstream_gene_variant | 0.21 |
rrl | 1473648 | n.-9_-7delTTG | upstream_gene_variant | 0.17 |
rrl | 1473731 | n.74T>A | 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 | 0.29 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673493 | c.-709C>T | upstream_gene_variant | 0.14 |
inhA | 1673499 | c.-703T>C | upstream_gene_variant | 0.16 |
inhA | 1673505 | c.-697A>T | upstream_gene_variant | 0.18 |
inhA | 1673517 | c.-685G>A | upstream_gene_variant | 0.17 |
inhA | 1673535 | c.-667A>G | upstream_gene_variant | 0.19 |
inhA | 1673547 | c.-655T>C | upstream_gene_variant | 0.21 |
inhA | 1673568 | c.-634C>G | upstream_gene_variant | 0.18 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.18 |
inhA | 1673685 | c.-517C>T | upstream_gene_variant | 0.17 |
inhA | 1673724 | c.-478A>G | upstream_gene_variant | 0.14 |
inhA | 1673730 | c.-472C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673733 | p.Met98Ile | missense_variant | 0.15 |
inhA | 1673736 | c.-466G>A | upstream_gene_variant | 0.16 |
inhA | 1673745 | c.-457G>A | upstream_gene_variant | 0.15 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.14 |
fabG1 | 1673749 | p.Lys104Arg | missense_variant | 0.15 |
inhA | 1674015 | c.-187C>A | upstream_gene_variant | 0.17 |
inhA | 1674018 | c.-184G>C | upstream_gene_variant | 0.17 |
inhA | 1674024 | c.-178T>C | upstream_gene_variant | 0.2 |
inhA | 1674033 | c.-169T>C | upstream_gene_variant | 0.16 |
fabG1 | 1674037 | p.Gln200Glu | missense_variant | 0.15 |
fabG1 | 1674079 | p.Pro214Ala | missense_variant | 0.14 |
inhA | 1674472 | p.Val91Leu | missense_variant | 0.14 |
inhA | 1674477 | c.276G>C | synonymous_variant | 0.19 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.19 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.18 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.17 |
inhA | 1674501 | c.300G>A | synonymous_variant | 0.17 |
inhA | 1674503 | p.Thr101Ser | missense_variant | 0.17 |
inhA | 1674513 | c.312C>G | synonymous_variant | 0.15 |
inhA | 1674675 | c.474C>T | synonymous_variant | 0.15 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.15 |
inhA | 1674852 | c.651G>A | synonymous_variant | 0.13 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.15 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.15 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.26 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.31 |
rpsA | 1833593 | p.Ser18Thr | missense_variant | 0.31 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.32 |
rpsA | 1833610 | c.69C>A | synonymous_variant | 0.35 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.21 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 0.21 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.25 |
rpsA | 1833718 | c.177C>T | synonymous_variant | 0.3 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.34 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.36 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.23 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.23 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.18 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.2 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.15 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.18 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834024 | c.483G>A | synonymous_variant | 0.17 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.22 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.21 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.27 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.23 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.22 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.17 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.2 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.15 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.17 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.26 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.27 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.33 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.25 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.24 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.24 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.2 |
rpsA | 1834495 | c.954G>A | synonymous_variant | 0.22 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.18 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.23 |
rpsA | 1834615 | c.1074C>T | synonymous_variant | 0.22 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.23 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.23 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.22 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.24 |
tlyA | 1917948 | c.9A>G | synonymous_variant | 0.16 |
tlyA | 1917965 | p.Ala9Val | missense_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917975 | c.36C>G | synonymous_variant | 0.18 |
tlyA | 1917981 | c.42G>C | synonymous_variant | 0.19 |
tlyA | 1917987 | c.48G>C | synonymous_variant | 0.18 |
tlyA | 1917996 | c.57A>C | synonymous_variant | 0.2 |
tlyA | 1918002 | p.Gln21His | missense_variant | 0.22 |
ndh | 2101744 | p.Asp433Glu | missense_variant | 0.14 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.15 |
katG | 2155649 | p.Tyr155His | missense_variant | 0.16 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.22 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.21 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.17 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.93 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.25 |
kasA | 2517956 | c.-159G>A | upstream_gene_variant | 0.24 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.23 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.21 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.21 |
kasA | 2518031 | c.-84G>T | upstream_gene_variant | 0.17 |
kasA | 2518034 | c.-81T>C | upstream_gene_variant | 0.19 |
kasA | 2518035 | c.-80C>G | upstream_gene_variant | 0.19 |
kasA | 2518041 | c.-74T>C | upstream_gene_variant | 0.2 |
kasA | 2518046 | c.-69C>G | upstream_gene_variant | 0.18 |
kasA | 2518049 | c.-66G>C | upstream_gene_variant | 0.18 |
kasA | 2518053 | c.-62_-60delATTinsCTC | upstream_gene_variant | 0.18 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.2 |
kasA | 2518252 | c.138C>T | synonymous_variant | 0.19 |
kasA | 2518279 | c.165T>C | synonymous_variant | 0.22 |
kasA | 2518283 | p.Ala57Pro | missense_variant | 0.2 |
kasA | 2518297 | c.183C>T | synonymous_variant | 0.16 |
kasA | 2518300 | c.186T>C | synonymous_variant | 0.15 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.17 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.21 |
kasA | 2518513 | c.399C>G | synonymous_variant | 0.2 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.17 |
kasA | 2518534 | c.420G>C | synonymous_variant | 0.22 |
kasA | 2518537 | c.423C>G | synonymous_variant | 0.22 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.29 |
kasA | 2518567 | c.453G>T | synonymous_variant | 0.27 |
kasA | 2518573 | c.459G>C | synonymous_variant | 0.26 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.26 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.4 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.39 |
kasA | 2518618 | c.504G>C | synonymous_variant | 0.5 |
kasA | 2518633 | c.519G>C | synonymous_variant | 0.5 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.53 |
kasA | 2518645 | c.531G>C | synonymous_variant | 0.62 |
kasA | 2518648 | c.534C>T | synonymous_variant | 0.57 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.55 |
kasA | 2518681 | c.567C>T | synonymous_variant | 0.53 |
kasA | 2518684 | c.570C>A | synonymous_variant | 0.53 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.5 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.54 |
kasA | 2518735 | c.621C>A | synonymous_variant | 0.48 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.41 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.37 |
kasA | 2518756 | c.642G>C | synonymous_variant | 0.32 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.25 |
kasA | 2518789 | c.675G>T | synonymous_variant | 0.26 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.25 |
kasA | 2518798 | c.684G>C | synonymous_variant | 0.24 |
kasA | 2518816 | c.702C>T | synonymous_variant | 0.19 |
kasA | 2518822 | c.708C>T | synonymous_variant | 0.19 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.19 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.24 |
kasA | 2518856 | p.Ile248Leu | missense_variant | 0.25 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.31 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.43 |
kasA | 2518894 | c.780G>A | synonymous_variant | 0.5 |
kasA | 2518903 | c.789C>T | synonymous_variant | 0.47 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.5 |
kasA | 2518910 | c.796C>T | synonymous_variant | 0.5 |
kasA | 2518939 | c.825T>C | synonymous_variant | 0.32 |
kasA | 2518942 | c.828T>C | synonymous_variant | 0.33 |
kasA | 2518951 | c.837G>A | synonymous_variant | 0.26 |
kasA | 2518960 | c.846C>G | synonymous_variant | 0.26 |
kasA | 2518963 | c.849T>C | synonymous_variant | 0.18 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.13 |
kasA | 2519266 | c.1152C>T | synonymous_variant | 0.14 |
ahpC | 2726142 | c.-51G>A | upstream_gene_variant | 1.0 |
pepQ | 2860317 | c.102A>C | synonymous_variant | 0.14 |
pepQ | 2860329 | c.90G>C | synonymous_variant | 0.2 |
pepQ | 2860332 | c.87C>T | synonymous_variant | 0.19 |
pepQ | 2860345 | p.Ser25Thr | missense_variant | 0.19 |
pepQ | 2860349 | p.Ile24Val | missense_variant | 0.19 |
pepQ | 2860364 | c.55T>C | synonymous_variant | 0.14 |
pepQ | 2860370 | p.Ser17Ala | missense_variant | 0.15 |
pepQ | 2860375 | p.Ala15Gly | missense_variant | 0.14 |
pepQ | 2860377 | c.42C>T | synonymous_variant | 0.14 |
pepQ | 2860389 | c.30G>C | synonymous_variant | 0.18 |
pepQ | 2860392 | p.Lys9Asn | missense_variant | 0.18 |
pepQ | 2860397 | p.Asp8His | missense_variant | 0.18 |
Rv2752c | 3064590 | c.1602C>T | synonymous_variant | 0.23 |
Rv2752c | 3064596 | c.1596G>C | synonymous_variant | 0.22 |
Rv2752c | 3064599 | c.1593A>G | synonymous_variant | 0.22 |
Rv2752c | 3064602 | c.1590T>G | synonymous_variant | 0.21 |
Rv2752c | 3064612 | p.Ile527Thr | missense_variant | 0.18 |
Rv2752c | 3064614 | c.1578G>C | synonymous_variant | 0.18 |
Rv2752c | 3064635 | c.1557G>C | synonymous_variant | 0.19 |
Rv2752c | 3064640 | c.1552T>C | synonymous_variant | 0.17 |
Rv2752c | 3064653 | c.1539A>G | synonymous_variant | 0.17 |
Rv2752c | 3064656 | c.1536G>A | synonymous_variant | 0.17 |
Rv2752c | 3064659 | c.1533G>C | synonymous_variant | 0.17 |
Rv2752c | 3065556 | c.636G>A | synonymous_variant | 0.24 |
Rv2752c | 3065580 | c.612G>C | synonymous_variant | 0.24 |
Rv2752c | 3065583 | c.609G>C | synonymous_variant | 0.22 |
Rv2752c | 3065594 | c.598C>T | synonymous_variant | 0.23 |
Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 0.23 |
Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 0.26 |
Rv2752c | 3065625 | c.567G>C | synonymous_variant | 0.22 |
Rv2752c | 3065634 | c.558G>C | synonymous_variant | 0.17 |
Rv2752c | 3065637 | c.555A>G | synonymous_variant | 0.14 |
Rv2752c | 3065640 | c.552T>C | synonymous_variant | 0.14 |
Rv2752c | 3065889 | c.303G>C | synonymous_variant | 0.15 |
Rv2752c | 3065892 | c.300C>T | synonymous_variant | 0.14 |
Rv2752c | 3065901 | c.291A>T | synonymous_variant | 0.17 |
Rv2752c | 3065916 | c.276T>C | synonymous_variant | 0.18 |
Rv2752c | 3065919 | c.273G>C | synonymous_variant | 0.19 |
Rv2752c | 3065925 | c.267G>C | synonymous_variant | 0.21 |
Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 0.25 |
Rv2752c | 3065952 | c.240C>G | synonymous_variant | 0.22 |
Rv2752c | 3065958 | c.234G>A | synonymous_variant | 0.81 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.15 |
thyX | 3067331 | c.615C>T | synonymous_variant | 0.17 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.27 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.27 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.27 |
thyX | 3067394 | c.552G>T | synonymous_variant | 0.27 |
thyX | 3067406 | c.540A>G | synonymous_variant | 0.32 |
thyX | 3067427 | c.519G>C | synonymous_variant | 0.29 |
thyX | 3067430 | c.516C>T | synonymous_variant | 0.29 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.23 |
thyX | 3067445 | c.501C>A | synonymous_variant | 0.25 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.2 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.2 |
thyX | 3067463 | p.Ile161Val | missense_variant | 0.15 |
thyX | 3067466 | c.480G>C | synonymous_variant | 0.18 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.29 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.18 |
thyA | 3074123 | p.Asp117Asn | missense_variant | 0.14 |
thyA | 3074151 | c.321G>A | synonymous_variant | 0.17 |
thyA | 3074157 | c.315C>G | synonymous_variant | 0.17 |
thyA | 3074160 | c.312A>T | synonymous_variant | 0.17 |
thyA | 3074172 | c.300G>C | synonymous_variant | 0.16 |
thyA | 3074283 | c.189G>A | synonymous_variant | 0.15 |
thyA | 3074286 | c.186T>C | synonymous_variant | 0.14 |
thyA | 3074297 | c.175C>T | synonymous_variant | 0.17 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448753 | p.Tyr84His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474138 | c.132T>G | synonymous_variant | 0.14 |
fprA | 3474147 | c.141G>A | synonymous_variant | 0.14 |
fprA | 3474150 | c.144G>T | synonymous_variant | 0.15 |
fprA | 3474162 | c.156G>C | synonymous_variant | 0.16 |
fprA | 3474168 | c.162G>C | synonymous_variant | 0.17 |
fprA | 3474174 | c.168T>C | synonymous_variant | 0.14 |
fprA | 3474997 | p.Gly331Arg | missense_variant | 0.14 |
fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 0.17 |
fbiB | 3641948 | c.414G>A | synonymous_variant | 0.14 |
fbiB | 3641951 | c.417G>C | synonymous_variant | 0.14 |
alr | 3840473 | c.948C>T | synonymous_variant | 0.14 |
alr | 3840513 | p.Arg303His | missense_variant | 0.14 |
alr | 3840515 | c.906A>G | synonymous_variant | 0.15 |
alr | 3840527 | c.894A>C | synonymous_variant | 0.16 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.21 |
rpoA | 3877567 | p.Ser314Thr | missense_variant | 0.26 |
rpoA | 3877569 | c.939G>C | synonymous_variant | 0.28 |
rpoA | 3877575 | c.933C>T | synonymous_variant | 0.26 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.28 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.29 |
rpoA | 3877602 | c.906C>T | synonymous_variant | 0.29 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.22 |
rpoA | 3877620 | c.888G>A | synonymous_variant | 0.21 |
rpoA | 3877647 | c.861C>A | synonymous_variant | 0.19 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.15 |
rpoA | 3877659 | c.849G>A | synonymous_variant | 0.17 |
rpoA | 3877830 | c.678C>T | synonymous_variant | 0.18 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.21 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.22 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.28 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.29 |
rpoA | 3877886 | c.622C>T | synonymous_variant | 0.24 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.26 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.26 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.27 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.29 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.25 |
rpoA | 3877929 | c.579C>T | synonymous_variant | 0.26 |
rpoA | 3877950 | c.558C>T | synonymous_variant | 0.21 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.21 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.24 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.23 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.23 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.22 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.21 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.2 |
rpoA | 3878043 | c.465G>T | synonymous_variant | 0.22 |
rpoA | 3878058 | c.450G>C | synonymous_variant | 0.26 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.24 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.26 |
rpoA | 3878085 | c.423G>A | synonymous_variant | 0.25 |
rpoA | 3878097 | c.411G>A | synonymous_variant | 0.26 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.27 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.27 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.28 |
rpoA | 3878126 | c.382C>T | synonymous_variant | 0.28 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.3 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.33 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.34 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.34 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.31 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.27 |
rpoA | 3878211 | c.297G>A | synonymous_variant | 0.27 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.22 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.24 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.21 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.2 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.15 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.18 |
rpoA | 3878376 | c.132G>A | synonymous_variant | 0.15 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.14 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 0.14 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.17 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.18 |
rpoA | 3878483 | c.25C>T | synonymous_variant | 0.18 |
rpoA | 3878490 | c.18C>T | synonymous_variant | 0.19 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.24 |
rpoA | 3878512 | c.-6_-5insGAA | upstream_gene_variant | 0.3 |
rpoA | 3878548 | c.-41C>A | upstream_gene_variant | 0.29 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.25 |
rpoA | 3878680 | c.-173C>T | upstream_gene_variant | 0.38 |
rpoA | 3878698 | c.-191A>C | upstream_gene_variant | 0.3 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.19 |
ddn | 3987092 | p.Glu83Asp | missense_variant | 1.0 |
clpC1 | 4038238 | p.Thr823Ala | missense_variant | 0.14 |
clpC1 | 4038239 | c.2466T>C | synonymous_variant | 0.15 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.35 |
clpC1 | 4038272 | c.2433T>C | synonymous_variant | 0.35 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.27 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.32 |
clpC1 | 4038308 | c.2397G>C | synonymous_variant | 0.31 |
clpC1 | 4038314 | c.2391T>G | synonymous_variant | 0.33 |
clpC1 | 4038335 | c.2370C>T | synonymous_variant | 0.31 |
clpC1 | 4038344 | c.2361G>A | synonymous_variant | 0.26 |
clpC1 | 4038350 | c.2355C>G | synonymous_variant | 0.19 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.19 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.19 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.17 |
clpC1 | 4038383 | c.2322G>A | synonymous_variant | 0.31 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.34 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.34 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.31 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.27 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.28 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.26 |
clpC1 | 4038436 | p.Ala757Ser | missense_variant | 0.3 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.32 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.33 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.28 |
clpC1 | 4038508 | c.2197C>T | synonymous_variant | 0.2 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.18 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.23 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.25 |
clpC1 | 4038800 | c.1905C>T | synonymous_variant | 0.29 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.31 |
clpC1 | 4038838 | c.1867C>T | synonymous_variant | 0.2 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.2 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.19 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.19 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.23 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.25 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.22 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.26 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.26 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.29 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.23 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.23 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.29 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.26 |
clpC1 | 4038995 | c.1710G>A | synonymous_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.33 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.35 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.35 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.38 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.39 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.38 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.41 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.36 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.3 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.29 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.28 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.27 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.28 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.3 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.27 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.25 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.18 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.18 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.15 |
clpC1 | 4039295 | c.1410A>G | synonymous_variant | 0.16 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.16 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.17 |
clpC1 | 4039337 | c.1368A>C | synonymous_variant | 0.23 |
clpC1 | 4039352 | c.1353C>T | synonymous_variant | 0.22 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.21 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.23 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.23 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.25 |
clpC1 | 4039442 | c.1261_1263delCTAinsTTG | synonymous_variant | 0.16 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.16 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.18 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.18 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.22 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.23 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.19 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.19 |
clpC1 | 4039493 | c.1212C>T | synonymous_variant | 0.19 |
clpC1 | 4039514 | c.1191C>T | synonymous_variant | 0.19 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.15 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.17 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.15 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.15 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.18 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.2 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.2 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.19 |
clpC1 | 4039868 | c.837C>T | synonymous_variant | 0.2 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.15 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.14 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.17 |
clpC1 | 4040531 | c.174T>G | synonymous_variant | 0.16 |
embC | 4240484 | p.Ala208Thr | missense_variant | 0.15 |
embC | 4240489 | c.627A>G | synonymous_variant | 0.15 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.14 |
embC | 4240512 | p.Ser217Thr | missense_variant | 0.15 |
embC | 4240516 | c.654G>C | synonymous_variant | 0.14 |
embC | 4240519 | c.657T>C | synonymous_variant | 0.14 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.14 |
embC | 4240741 | c.879C>T | synonymous_variant | 0.19 |
embC | 4240777 | c.915G>A | synonymous_variant | 0.22 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.2 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.19 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.16 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.16 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.19 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.28 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.28 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.19 |
embC | 4241153 | p.Ile431Leu | missense_variant | 0.25 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.22 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.22 |
embC | 4241167 | c.1305C>G | synonymous_variant | 0.23 |
embC | 4241185 | c.1323G>C | synonymous_variant | 0.22 |
embC | 4241197 | c.1335G>C | synonymous_variant | 0.16 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.17 |
embA | 4244159 | c.927G>T | synonymous_variant | 0.12 |
embA | 4244669 | c.1437G>C | synonymous_variant | 0.15 |
embA | 4244675 | c.1443A>G | synonymous_variant | 0.15 |
embA | 4244681 | c.1449A>G | synonymous_variant | 0.15 |
embA | 4244684 | c.1452C>G | synonymous_variant | 0.16 |
embA | 4244702 | c.1470C>G | synonymous_variant | 0.17 |
embA | 4244705 | c.1473G>C | synonymous_variant | 0.16 |
embA | 4244708 | c.1476C>G | synonymous_variant | 0.15 |
embA | 4244714 | c.1482C>G | synonymous_variant | 0.15 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.17 |
embA | 4245186 | p.Thr652Ala | missense_variant | 0.17 |
embB | 4245623 | c.-891G>A | upstream_gene_variant | 0.14 |
embB | 4245662 | c.-852G>C | upstream_gene_variant | 0.21 |
embB | 4245674 | c.-840A>T | upstream_gene_variant | 0.22 |
embB | 4245677 | c.-837G>C | upstream_gene_variant | 0.22 |
embB | 4245683 | c.-831C>T | upstream_gene_variant | 0.22 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.27 |
embB | 4245714 | c.-800C>T | upstream_gene_variant | 0.28 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.28 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.28 |
embB | 4245734 | c.-780G>C | upstream_gene_variant | 0.21 |
embB | 4245737 | c.-777A>T | upstream_gene_variant | 0.2 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.24 |
embA | 4245772 | p.Asn847Thr | missense_variant | 0.2 |
embB | 4246028 | c.-486G>C | upstream_gene_variant | 0.13 |
embB | 4246070 | c.-444G>C | upstream_gene_variant | 0.17 |
embB | 4246109 | c.-405C>G | upstream_gene_variant | 0.15 |
embB | 4246115 | c.-399T>C | upstream_gene_variant | 0.14 |
embB | 4246172 | c.-342C>T | upstream_gene_variant | 0.25 |
embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.21 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.22 |
embB | 4246211 | c.-303T>C | upstream_gene_variant | 0.22 |
embB | 4246217 | c.-297G>A | upstream_gene_variant | 0.24 |
embB | 4246220 | c.-294T>C | upstream_gene_variant | 0.25 |
embB | 4246223 | c.-291C>T | upstream_gene_variant | 0.24 |
embA | 4246227 | p.Ile999Val | missense_variant | 0.23 |
embB | 4246235 | c.-279G>A | upstream_gene_variant | 0.23 |
embB | 4246244 | c.-270G>A | upstream_gene_variant | 0.2 |
embA | 4246254 | p.Leu1008Met | missense_variant | 0.15 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.14 |
embB | 4247137 | c.624C>G | synonymous_variant | 0.21 |
embB | 4247140 | c.627G>C | synonymous_variant | 0.19 |
embB | 4247150 | p.Arg213Thr | missense_variant | 0.18 |
embB | 4247155 | c.642G>A | synonymous_variant | 0.18 |
embB | 4247355 | p.Ala281Gly | missense_variant | 0.14 |
embB | 4247365 | c.852A>C | synonymous_variant | 0.15 |
embB | 4247370 | p.Gly286Ala | missense_variant | 0.14 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.16 |
embB | 4247398 | c.885G>C | synonymous_variant | 0.17 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.17 |
embB | 4247404 | c.891G>C | synonymous_variant | 0.17 |
embB | 4247407 | c.894G>C | synonymous_variant | 0.18 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.21 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.23 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.26 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.28 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.27 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.18 |
embB | 4247555 | p.Leu348Ile | missense_variant | 0.18 |
embB | 4247566 | c.1053C>G | synonymous_variant | 0.16 |
embB | 4247579 | p.Ala356Phe | missense_variant | 0.17 |
embB | 4247657 | p.Pro382Ala | missense_variant | 0.16 |
embB | 4247684 | c.1171T>C | synonymous_variant | 0.15 |
embB | 4247785 | c.1272G>C | synonymous_variant | 0.17 |
embB | 4247800 | c.1287A>C | synonymous_variant | 0.18 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.14 |
embB | 4247915 | p.Arg468Ser | missense_variant | 0.14 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.17 |
embB | 4247948 | p.Val479Leu | missense_variant | 0.18 |
embB | 4247975 | p.Val488Ile | missense_variant | 0.17 |
embB | 4247989 | c.1476G>C | synonymous_variant | 0.17 |
embB | 4248042 | p.Ala510Gly | missense_variant | 0.23 |
embB | 4248052 | c.1539G>T | synonymous_variant | 0.22 |
embB | 4248055 | c.1542G>C | synonymous_variant | 0.23 |
embB | 4248058 | c.1545C>T | synonymous_variant | 0.19 |
embB | 4248061 | c.1548G>A | synonymous_variant | 0.17 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.15 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.17 |
embB | 4248094 | c.1581C>T | synonymous_variant | 0.17 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.2 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.19 |
embB | 4248334 | c.1821C>G | synonymous_variant | 0.19 |
embB | 4248349 | c.1836G>A | synonymous_variant | 0.19 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.14 |
embB | 4248379 | c.1866G>A | synonymous_variant | 0.15 |
embB | 4248424 | c.1911G>A | synonymous_variant | 0.17 |
embB | 4248430 | c.1917T>C | synonymous_variant | 0.16 |
embB | 4248448 | c.1935C>T | synonymous_variant | 0.2 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.2 |
embB | 4248472 | c.1959T>C | synonymous_variant | 0.19 |
embB | 4248496 | c.1983G>C | synonymous_variant | 0.17 |
embB | 4248504 | p.Asp664Ala | missense_variant | 0.15 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.15 |
embB | 4249429 | c.2916C>G | synonymous_variant | 0.16 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.16 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.16 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.15 |
embB | 4249453 | c.2940G>C | synonymous_variant | 0.16 |
embB | 4249568 | p.Ser1019Asn | missense_variant | 0.19 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.18 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.19 |
embB | 4249609 | c.3096T>C | synonymous_variant | 0.14 |
embB | 4249618 | c.3105C>G | synonymous_variant | 0.14 |
embB | 4249624 | c.3111C>T | synonymous_variant | 0.14 |
embB | 4249640 | c.3127T>C | synonymous_variant | 0.17 |
embB | 4249648 | c.3135G>C | synonymous_variant | 0.17 |
embB | 4249675 | c.3162C>G | synonymous_variant | 0.17 |
embB | 4249693 | c.3180T>C | synonymous_variant | 0.18 |
embB | 4249699 | c.3186T>A | synonymous_variant | 0.2 |
embB | 4249702 | c.3189C>A | synonymous_variant | 0.2 |
embB | 4249703 | c.3190C>T | synonymous_variant | 0.2 |
embB | 4249711 | c.3198G>A | synonymous_variant | 0.18 |
aftB | 4267592 | c.1245C>G | synonymous_variant | 0.21 |
aftB | 4267622 | p.Ser405Thr | missense_variant | 0.22 |
aftB | 4267634 | p.Arg401His | missense_variant | 0.21 |
aftB | 4267637 | c.1200C>G | synonymous_variant | 0.21 |
aftB | 4267649 | c.1188T>C | synonymous_variant | 0.24 |
aftB | 4267667 | c.1170A>G | synonymous_variant | 0.21 |
aftB | 4267670 | c.1167G>A | synonymous_variant | 0.17 |
aftB | 4267891 | p.Val316Ile | missense_variant | 0.25 |
aftB | 4267892 | p.Ile315Met | missense_variant | 0.25 |
aftB | 4267898 | c.939T>C | synonymous_variant | 0.18 |
aftB | 4267907 | c.930C>G | synonymous_variant | 0.18 |
aftB | 4267912 | p.Pro309Ala | missense_variant | 0.18 |
aftB | 4267916 | c.921T>C | synonymous_variant | 0.15 |
aftB | 4268994 | c.-158T>C | upstream_gene_variant | 0.16 |
aftB | 4269000 | c.-164G>A | upstream_gene_variant | 0.14 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.14 |
aftB | 4269045 | c.-209G>C | upstream_gene_variant | 0.14 |
aftB | 4269150 | c.-314G>C | upstream_gene_variant | 0.22 |
aftB | 4269162 | c.-328_-326delTTGinsCTC | upstream_gene_variant | 0.24 |
aftB | 4269177 | c.-341G>A | upstream_gene_variant | 0.29 |
aftB | 4269180 | c.-344G>T | upstream_gene_variant | 0.38 |
aftB | 4269195 | c.-359C>T | upstream_gene_variant | 0.42 |
aftB | 4269216 | c.-380C>T | upstream_gene_variant | 0.39 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.38 |
aftB | 4269225 | c.-389C>T | upstream_gene_variant | 0.35 |
aftB | 4269231 | c.-395C>T | upstream_gene_variant | 0.37 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.39 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.45 |
aftB | 4269248 | c.-412C>T | upstream_gene_variant | 0.38 |
aftB | 4269261 | c.-425G>A | upstream_gene_variant | 0.33 |
aftB | 4269285 | c.-449T>G | upstream_gene_variant | 0.19 |
ethA | 4326510 | p.Ala322Pro | missense_variant | 0.17 |
ethA | 4326520 | p.Glu318Asp | missense_variant | 0.2 |
ethA | 4326523 | c.951T>C | synonymous_variant | 0.19 |
ethA | 4326535 | c.939G>C | synonymous_variant | 0.22 |
ethR | 4326556 | c.-993A>G | upstream_gene_variant | 0.17 |
ethA | 4326563 | p.Ala304Gly | missense_variant | 0.15 |
ethR | 4326565 | c.-984C>A | upstream_gene_variant | 0.15 |
ethA | 4327065 | p.Cys137Arg | missense_variant | 0.97 |
ethR | 4327306 | c.-243G>A | upstream_gene_variant | 0.17 |
ethR | 4327318 | c.-231T>G | upstream_gene_variant | 0.21 |
ethR | 4327327 | c.-222A>G | upstream_gene_variant | 0.21 |
ethR | 4327330 | c.-219G>A | upstream_gene_variant | 0.21 |
ethR | 4327335 | c.-214A>G | upstream_gene_variant | 0.21 |
ethR | 4327336 | c.-213A>G | upstream_gene_variant | 0.21 |
ethA | 4327356 | p.Ser40Ala | missense_variant | 0.2 |
ethA | 4327357 | p.Glu39Ser | missense_variant | 0.21 |
ethR | 4327390 | c.-159C>G | upstream_gene_variant | 0.27 |
ethR | 4327396 | c.-153A>G | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |