Run ID: ERR4831724
Sample name:
Date: 01-04-2023 21:05:02
Number of reads: 677725
Percentage reads mapped: 95.26
Strain: lineage2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
embB | 4247429 | p.Met306Val | missense_variant | 0.67 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5111 | c.-129C>A | upstream_gene_variant | 0.14 |
gyrB | 5855 | p.Ile206Leu | missense_variant | 0.11 |
gyrA | 6517 | c.-785G>A | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7707 | p.Pro136Ala | missense_variant | 0.12 |
gyrA | 7856 | p.Met185Ile | missense_variant | 0.15 |
gyrA | 8602 | p.Ala434Val | missense_variant | 0.17 |
gyrA | 8731 | p.Gly477Val | missense_variant | 0.25 |
gyrA | 8871 | p.Gly524Arg | missense_variant | 0.1 |
gyrA | 9264 | p.Asp655Tyr | missense_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9380 | p.Met693Ile | missense_variant | 0.17 |
gyrA | 9395 | c.2094G>T | synonymous_variant | 0.18 |
gyrA | 9563 | p.Met754Ile | missense_variant | 0.13 |
fgd1 | 490647 | c.-136C>A | upstream_gene_variant | 0.29 |
fgd1 | 490856 | p.Val25Ala | missense_variant | 0.29 |
fgd1 | 491661 | c.879C>A | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619759 | c.-132C>A | upstream_gene_variant | 0.33 |
ccsA | 620368 | p.Ala160Thr | missense_variant | 0.18 |
ccsA | 620605 | p.Val239Ile | missense_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620805 | c.915C>T | synonymous_variant | 0.15 |
rpoB | 759850 | p.Pro15Leu | missense_variant | 0.4 |
rpoB | 760823 | c.1017G>C | synonymous_variant | 0.25 |
rpoB | 760833 | p.His343Tyr | missense_variant | 0.17 |
rpoB | 761129 | c.1323G>T | synonymous_variant | 0.12 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.22 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.33 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.22 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.29 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.33 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.33 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.25 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.38 |
rpoB | 761243 | c.1437G>A | synonymous_variant | 0.25 |
rpoB | 761345 | c.1539G>A | synonymous_variant | 0.12 |
rpoB | 761620 | p.Met605Thr | missense_variant | 0.29 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.4 |
rpoB | 762500 | p.Met898Ile | missense_variant | 0.22 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.14 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763897 | p.Lys176Asn | missense_variant | 0.2 |
rpoC | 763972 | c.603C>T | synonymous_variant | 0.25 |
rpoC | 764143 | c.774G>C | synonymous_variant | 0.17 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 0.17 |
rpoC | 764150 | p.Ile261Val | missense_variant | 0.14 |
rpoC | 764165 | p.Glu266Gln | missense_variant | 0.14 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.25 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.29 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.36 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.36 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.24 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.24 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.15 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.17 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.17 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.17 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.22 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.12 |
rpoC | 765370 | c.2001G>C | synonymous_variant | 0.29 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.22 |
rpoC | 765382 | c.2013G>T | synonymous_variant | 0.22 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.18 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.2 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.2 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.17 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.12 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.11 |
rpoC | 765654 | p.Arg762His | missense_variant | 0.18 |
rpoC | 765682 | c.2313C>T | synonymous_variant | 0.15 |
rpoC | 765702 | p.Trp778Leu | missense_variant | 0.15 |
rpoC | 766775 | p.Arg1136Cys | missense_variant | 0.22 |
rpoC | 766817 | p.His1150Tyr | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776177 | c.2304G>A | synonymous_variant | 0.25 |
mmpL5 | 776755 | p.Asp576Asn | missense_variant | 0.14 |
mmpL5 | 777676 | p.Leu269Met | missense_variant | 0.17 |
mmpL5 | 777746 | c.735G>T | synonymous_variant | 0.5 |
mmpR5 | 778208 | c.-782C>T | upstream_gene_variant | 0.33 |
mmpL5 | 778269 | p.Ser71Leu | missense_variant | 0.25 |
mmpL5 | 778396 | p.Arg29Gly | missense_variant | 0.17 |
mmpL5 | 779467 | c.-987G>T | upstream_gene_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781661 | c.102C>T | synonymous_variant | 0.17 |
rplC | 800777 | c.-32C>T | upstream_gene_variant | 0.12 |
fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.25 |
fbiC | 1303710 | p.Leu260Phe | missense_variant | 0.33 |
fbiC | 1304799 | c.1869G>T | synonymous_variant | 0.22 |
fbiC | 1304946 | c.2016G>A | synonymous_variant | 0.17 |
fbiC | 1305168 | c.2238C>T | synonymous_variant | 0.22 |
Rv1258c | 1406293 | p.Gly350Trp | missense_variant | 0.15 |
Rv1258c | 1406356 | p.Gln329* | stop_gained | 0.2 |
Rv1258c | 1406732 | c.609G>T | synonymous_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.8 |
Rv1258c | 1407488 | c.-148C>A | upstream_gene_variant | 0.22 |
Rv1258c | 1407515 | c.-175G>T | upstream_gene_variant | 0.2 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.1 |
embR | 1416591 | p.Arg253Trp | missense_variant | 0.2 |
embR | 1416643 | c.705G>A | synonymous_variant | 0.22 |
embR | 1416739 | c.609C>T | synonymous_variant | 0.2 |
embR | 1416824 | p.Thr175Ile | missense_variant | 0.11 |
embR | 1417127 | p.Ser74Tyr | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472534 | n.689G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473860 | n.203C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474031 | n.374T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474084 | n.431delA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474591 | n.934G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475950 | n.2293C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1674108 | p.Phe223Leu | missense_variant | 0.25 |
fabG1 | 1674176 | p.Gly246Ala | missense_variant | 0.11 |
inhA | 1674281 | p.Arg27Pro | missense_variant | 0.14 |
rpsA | 1833463 | c.-79C>T | upstream_gene_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834258 | p.Glu239Asp | missense_variant | 0.17 |
rpsA | 1834291 | p.Glu250Asp | missense_variant | 0.13 |
rpsA | 1834322 | p.Glu261* | stop_gained | 0.13 |
rpsA | 1834367 | p.Leu276Phe | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918074 | c.135C>T | synonymous_variant | 0.33 |
ndh | 2101711 | c.1332G>A | synonymous_variant | 0.15 |
ndh | 2101889 | p.Val385Ala | missense_variant | 0.25 |
ndh | 2101965 | p.Glu360Lys | missense_variant | 0.17 |
ndh | 2102857 | p.Ile62Met | missense_variant | 0.12 |
katG | 2153994 | c.2118G>A | synonymous_variant | 0.18 |
katG | 2154491 | p.Ala541Ser | missense_variant | 0.14 |
katG | 2154673 | p.Ala480Glu | missense_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154929 | p.Arg395Ser | missense_variant | 0.13 |
katG | 2155168 | p.Ser315Ala | missense_variant | 0.12 |
katG | 2155877 | p.Asp79Tyr | missense_variant | 0.2 |
katG | 2156268 | c.-157G>A | upstream_gene_variant | 0.17 |
katG | 2156362 | c.-251C>T | upstream_gene_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168075 | c.2538G>A | synonymous_variant | 0.22 |
PPE35 | 2168224 | p.Pro797Ser | missense_variant | 0.14 |
PPE35 | 2170331 | c.282G>A | synonymous_variant | 0.13 |
PPE35 | 2170453 | p.Gly54Ser | missense_variant | 0.33 |
Rv1979c | 2222820 | c.345G>T | synonymous_variant | 0.12 |
Rv1979c | 2223271 | c.-107G>A | upstream_gene_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288806 | p.Ala146Ser | missense_variant | 0.12 |
pncA | 2289446 | c.-205G>A | upstream_gene_variant | 0.14 |
pncA | 2289909 | c.-668G>A | upstream_gene_variant | 0.14 |
pncA | 2289977 | c.-736C>A | upstream_gene_variant | 0.12 |
pncA | 2289992 | c.-751G>C | upstream_gene_variant | 0.12 |
eis | 2714224 | p.Ala370Val | missense_variant | 0.15 |
eis | 2714344 | p.Ala330Val | missense_variant | 0.17 |
eis | 2714357 | p.Gly326Ser | missense_variant | 0.12 |
eis | 2714420 | p.Leu305Ile | missense_variant | 0.25 |
eis | 2714636 | p.Leu233Ile | missense_variant | 0.13 |
eis | 2715330 | c.3G>A | synonymous_variant | 0.17 |
eis | 2715519 | c.-187G>C | upstream_gene_variant | 0.2 |
folC | 2746411 | c.1188G>A | synonymous_variant | 0.2 |
folC | 2746469 | p.Gly377Val | missense_variant | 0.22 |
folC | 2746593 | p.Pro336Ser | missense_variant | 0.17 |
folC | 2746893 | p.Arg236Cys | missense_variant | 0.25 |
folC | 2747287 | c.312G>A | synonymous_variant | 0.22 |
folC | 2747395 | c.204T>C | synonymous_variant | 0.33 |
pepQ | 2859479 | p.Gly314Ser | missense_variant | 0.33 |
pepQ | 2860072 | p.Gly116Asp | missense_variant | 0.18 |
pepQ | 2860130 | p.Phe97Ile | missense_variant | 0.13 |
pepQ | 2860226 | p.Ala65Ser | missense_variant | 0.33 |
pepQ | 2860524 | c.-106A>T | upstream_gene_variant | 0.13 |
ribD | 2987144 | p.Gln102His | missense_variant | 0.4 |
ribD | 2987256 | p.Pro140Ser | missense_variant | 0.18 |
Rv2752c | 3064708 | p.Arg495Pro | missense_variant | 0.2 |
Rv2752c | 3065129 | c.1063C>T | synonymous_variant | 1.0 |
Rv2752c | 3065192 | p.Ile334Val | missense_variant | 0.13 |
Rv2752c | 3065537 | p.Gly219Ser | missense_variant | 0.17 |
Rv2752c | 3065573 | p.Glu207Gln | missense_variant | 0.17 |
Rv2752c | 3066361 | c.-170G>C | upstream_gene_variant | 0.25 |
Rv2752c | 3067037 | c.-846G>T | upstream_gene_variant | 0.5 |
thyX | 3067640 | c.306G>A | synonymous_variant | 0.14 |
thyX | 3067852 | p.Gly32Arg | missense_variant | 0.29 |
thyX | 3068074 | c.-129C>G | upstream_gene_variant | 0.17 |
thyA | 3073704 | c.768G>T | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086821 | c.6_7dupCG | frameshift_variant | 0.17 |
ald | 3086880 | p.Ala21Ser | missense_variant | 0.12 |
ald | 3087066 | p.Gly83Cys | missense_variant | 0.25 |
ald | 3087322 | p.Pro168Leu | missense_variant | 0.5 |
ald | 3087377 | c.558C>T | synonymous_variant | 0.25 |
ald | 3087782 | c.963G>A | synonymous_variant | 0.13 |
ald | 3087812 | c.993G>A | synonymous_variant | 0.18 |
ald | 3087930 | p.Ala371Thr | missense_variant | 0.25 |
fbiD | 3339250 | p.Asp45Tyr | missense_variant | 0.15 |
Rv3083 | 3449144 | p.Pro214Gln | missense_variant | 0.17 |
Rv3083 | 3449278 | p.Arg259Trp | missense_variant | 0.4 |
fprA | 3473932 | c.-75G>A | upstream_gene_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474467 | p.Gly154Asp | missense_variant | 0.12 |
fprA | 3474810 | c.804G>T | synonymous_variant | 0.17 |
fprA | 3475166 | p.Gly387Asp | missense_variant | 0.15 |
whiB7 | 3568500 | c.180T>C | synonymous_variant | 0.2 |
whiB7 | 3568782 | c.-103G>T | upstream_gene_variant | 0.13 |
Rv3236c | 3612037 | p.Phe360Leu | missense_variant | 0.78 |
Rv3236c | 3612379 | c.738G>C | synonymous_variant | 0.25 |
Rv3236c | 3612398 | p.Ala240Val | missense_variant | 0.5 |
Rv3236c | 3612784 | p.Leu111Phe | missense_variant | 0.33 |
Rv3236c | 3612809 | p.Pro103Leu | missense_variant | 0.29 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613046 | p.Val24Glu | missense_variant | 0.25 |
fbiA | 3640488 | c.-55G>T | upstream_gene_variant | 0.2 |
fbiA | 3640800 | p.Trp86Cys | missense_variant | 0.25 |
fbiB | 3641838 | p.Val102Ile | missense_variant | 0.12 |
fbiB | 3642678 | p.Gln382Lys | missense_variant | 0.33 |
alr | 3840941 | c.480C>T | synonymous_variant | 0.18 |
alr | 3841241 | p.Gln60His | missense_variant | 0.13 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.14 |
rpoA | 3877502 | p.Tyr336His | missense_variant | 0.2 |
rpoA | 3877542 | c.966C>A | synonymous_variant | 0.25 |
rpoA | 3877545 | c.963G>T | synonymous_variant | 0.25 |
rpoA | 3877554 | c.954G>A | synonymous_variant | 0.22 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 0.29 |
rpoA | 3877563 | c.945C>T | synonymous_variant | 0.29 |
rpoA | 3877569 | p.Pro313Thr | missense_variant | 0.29 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.22 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.36 |
rpoA | 3877614 | c.894G>A | synonymous_variant | 0.17 |
rpoA | 3877620 | c.888G>A | synonymous_variant | 0.17 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.2 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.29 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.29 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.33 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.33 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.33 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.29 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.15 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 0.15 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.15 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.17 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.12 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.13 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.14 |
rpoA | 3877755 | c.753C>T | synonymous_variant | 0.13 |
rpoA | 3877758 | c.750G>C | synonymous_variant | 0.13 |
rpoA | 3877764 | c.744C>A | synonymous_variant | 0.17 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.18 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.15 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.15 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.15 |
rpoA | 3877797 | c.711G>A | synonymous_variant | 0.18 |
rpoA | 3877815 | c.693C>T | synonymous_variant | 0.2 |
rpoA | 3877867 | p.Thr214Lys | missense_variant | 0.12 |
rpoA | 3878267 | p.Lys81Glu | missense_variant | 0.15 |
ddn | 3986687 | c.-157C>A | upstream_gene_variant | 0.17 |
clpC1 | 4038383 | c.2322G>T | synonymous_variant | 0.17 |
clpC1 | 4038498 | p.Ser736Ile | missense_variant | 1.0 |
clpC1 | 4038602 | c.2103G>T | synonymous_variant | 0.15 |
clpC1 | 4038754 | p.Gln651* | stop_gained | 0.15 |
clpC1 | 4039242 | p.Leu488Arg | missense_variant | 0.18 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.14 |
clpC1 | 4040495 | c.210C>T | synonymous_variant | 0.12 |
clpC1 | 4040705 | c.-1G>A | upstream_gene_variant | 0.14 |
panD | 4043882 | p.Pro134Ser | missense_variant | 0.22 |
panD | 4044443 | c.-162G>T | upstream_gene_variant | 0.18 |
embC | 4239665 | c.-198G>A | upstream_gene_variant | 0.18 |
embC | 4239696 | c.-167C>T | upstream_gene_variant | 0.17 |
embC | 4239852 | c.-11G>T | upstream_gene_variant | 0.25 |
embC | 4240139 | p.Gly93Arg | missense_variant | 0.17 |
embC | 4240217 | p.Arg119Cys | missense_variant | 0.14 |
embC | 4240265 | p.Arg135Cys | missense_variant | 0.15 |
embC | 4240342 | c.480C>T | synonymous_variant | 0.14 |
embC | 4240569 | p.Leu236Arg | missense_variant | 0.33 |
embC | 4240756 | c.894G>C | synonymous_variant | 0.12 |
embC | 4240771 | c.909G>C | synonymous_variant | 0.14 |
embC | 4240772 | p.Ser304Ala | missense_variant | 0.14 |
embC | 4240778 | p.His306Gly | missense_variant | 0.14 |
embC | 4240781 | p.Ala307Ser | missense_variant | 0.15 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.13 |
embC | 4240871 | p.Val337Phe | missense_variant | 0.13 |
embC | 4241524 | c.1662G>A | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242836 | p.Pro992Thr | missense_variant | 0.2 |
embA | 4243348 | p.Thr39Ile | missense_variant | 1.0 |
embA | 4243471 | p.Ala80Val | missense_variant | 1.0 |
embA | 4244018 | p.Leu262Phe | missense_variant | 0.15 |
embA | 4244479 | p.Thr416Met | missense_variant | 0.4 |
embA | 4244781 | p.Arg517Cys | missense_variant | 0.13 |
embA | 4245071 | c.1839G>C | synonymous_variant | 0.11 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.18 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.17 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.19 |
embA | 4245094 | p.Ile621Thr | missense_variant | 0.19 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.19 |
embA | 4245125 | c.1893G>C | synonymous_variant | 0.23 |
embA | 4245179 | p.Met649Ile | missense_variant | 0.13 |
embA | 4245242 | p.Tyr670* | stop_gained | 0.15 |
embA | 4245444 | p.Asp738Asn | missense_variant | 0.5 |
embA | 4245661 | p.Ala810Val | missense_variant | 0.22 |
embB | 4245812 | c.-702G>T | upstream_gene_variant | 0.22 |
embA | 4246085 | p.Glu951Asp | missense_variant | 0.17 |
embA | 4246513 | p.Pro1094Leu | missense_variant | 0.29 |
embB | 4246774 | c.261G>A | synonymous_variant | 0.2 |
embB | 4246870 | p.Ser119Arg | missense_variant | 0.22 |
embB | 4246875 | p.Gln121Arg | missense_variant | 0.22 |
embB | 4247689 | c.1176G>A | synonymous_variant | 0.29 |
embB | 4249616 | p.Gly1035Ser | missense_variant | 0.13 |
embB | 4249688 | p.Arg1059Ser | missense_variant | 0.14 |
aftB | 4267380 | p.Val486Glu | missense_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268280 | p.Arg186Gln | missense_variant | 0.15 |
ubiA | 4269647 | p.Ser63Arg | missense_variant | 0.25 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 0.92 |
ethR | 4326898 | c.-651C>T | upstream_gene_variant | 0.25 |
ethA | 4327179 | p.Arg99Gly | missense_variant | 0.12 |
ethA | 4328157 | c.-684C>T | upstream_gene_variant | 0.18 |
whiB6 | 4338194 | p.Arg110Trp | missense_variant | 0.25 |
whiB6 | 4338427 | p.Gly32Val | missense_variant | 0.17 |
whiB6 | 4338582 | c.-61G>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407851 | p.Arg118Cys | missense_variant | 0.14 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408049 | p.Cys52Arg | missense_variant | 0.11 |
gid | 4408436 | c.-234C>T | upstream_gene_variant | 0.17 |