Run ID: ERR11068570
Sample name:
Date: 06-04-2023 17:45:14
Number of reads: 2564319
Percentage reads mapped: 93.1
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.17 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620682 | c.792G>A | synonymous_variant | 0.15 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.19 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.17 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.14 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.13 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.13 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.13 |
ccsA | 620742 | c.852G>C | synonymous_variant | 0.13 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.13 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.13 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.13 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.14 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.13 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760381 | p.Thr192Met | missense_variant | 0.12 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.13 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.12 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.15 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.16 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.13 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.15 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.16 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.2 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.2 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.21 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.22 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.21 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.19 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.19 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.19 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.17 |
rpoB | 761373 | p.Val523His | missense_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.12 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.12 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.13 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.13 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.14 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.12 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.15 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.15 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.16 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.15 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.15 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.14 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.16 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.14 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.16 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.14 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.14 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.19 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.17 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.18 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.17 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.14 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.13 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.12 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.13 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.15 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.16 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.16 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.15 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.15 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.16 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.17 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.17 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.16 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.13 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.13 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.14 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.14 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.14 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.16 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.16 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.14 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.14 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.17 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.16 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.18 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.16 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.2 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.19 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.18 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.16 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.12 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.14 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.14 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.13 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.12 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.15 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.14 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.14 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.15 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.16 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.16 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.19 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.2 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.22 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.23 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.24 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.29 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.3 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.26 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.26 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.2 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.19 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.22 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.24 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.2 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.21 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.23 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.23 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.26 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.23 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.23 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.2 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.21 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.19 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.17 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.16 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.14 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.14 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.16 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.17 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.19 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.2 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.2 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.21 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.18 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.18 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.19 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.2 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.21 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.23 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.24 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.26 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.25 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.21 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.19 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.15 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.13 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.13 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.14 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.16 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.13 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.14 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.13 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.14 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.13 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.12 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.13 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.14 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.14 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.2 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.21 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.22 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.24 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.19 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.18 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.18 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.15 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.16 |
rplC | 801309 | c.501C>G | synonymous_variant | 0.14 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.14 |
rplC | 801321 | c.513C>T | synonymous_variant | 0.14 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.14 |
fbiC | 1303797 | c.867A>G | synonymous_variant | 0.13 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.14 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.15 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.16 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.16 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.16 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.15 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.17 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.12 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.14 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.14 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.14 |
atpE | 1461158 | c.114T>G | synonymous_variant | 0.14 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.14 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.15 |
atpE | 1461185 | c.141G>T | synonymous_variant | 0.13 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.14 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473637 | n.-21A>G | upstream_gene_variant | 1.0 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.15 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.16 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.18 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.19 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.21 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.19 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.19 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.18 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.15 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.16 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.15 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.2 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.2 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.23 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.21 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.21 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.22 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.24 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.23 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.22 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.2 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.18 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.15 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.13 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.14 |
rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 0.14 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.14 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.13 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.13 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.13 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.14 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.15 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.14 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154735 | p.Lys459Asn | missense_variant | 1.0 |
katG | 2154915 | c.1197A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.16 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.2 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.24 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.24 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.19 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.19 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.22 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.15 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.15 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.13 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.14 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.16 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.16 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.16 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.15 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.16 |
rpoA | 3878043 | c.465G>A | synonymous_variant | 0.15 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.15 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.15 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.16 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.15 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.15 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.16 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.15 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.12 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.14 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.13 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.13 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.13 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.13 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.14 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.18 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.18 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.19 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.18 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.2 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.19 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.18 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.19 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.16 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.13 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.13 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.14 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.15 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.16 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.15 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.18 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.13 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.13 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.13 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.14 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.16 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.18 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.17 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.17 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.17 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.18 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.19 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.14 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.15 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.16 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.18 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.28 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |