Run ID: ERR4819280
Sample name:
Date: 01-04-2023 16:01:25
Number of reads: 243141
Percentage reads mapped: 72.31
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.4 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.4 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.4 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 0.4 |
gyrB | 6754 | c.1516delA | frameshift_variant | 0.33 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.33 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.33 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.5 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.4 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.33 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.33 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.4 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.4 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.4 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.2 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.33 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.33 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.4 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.4 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.4 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.5 |
gyrA | 7697 | c.396C>A | synonymous_variant | 0.67 |
gyrA | 8666 | c.1365G>C | synonymous_variant | 0.4 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.67 |
gyrA | 8694 | c.1393C>T | synonymous_variant | 0.67 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
gyrA | 8723 | c.1422G>A | synonymous_variant | 1.0 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.67 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.67 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.67 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.4 |
gyrA | 8807 | c.1506C>T | synonymous_variant | 0.4 |
gyrA | 8810 | c.1509A>G | synonymous_variant | 0.4 |
gyrA | 8816 | c.1515C>G | synonymous_variant | 0.5 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.5 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.6 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.5 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.4 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.5 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.5 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.5 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.4 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.5 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.67 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.5 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.5 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.5 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.5 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.5 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.5 |
gyrA | 9293 | c.1992G>C | synonymous_variant | 0.5 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490800 | c.18A>C | synonymous_variant | 0.5 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.5 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.5 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.5 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.6 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 1.0 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 1.0 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 1.0 |
fgd1 | 491535 | c.753G>C | synonymous_variant | 0.33 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.25 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.29 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.33 |
fgd1 | 491553 | c.771G>A | synonymous_variant | 0.29 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.2 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.22 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.22 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.22 |
mshA | 575809 | c.462C>T | synonymous_variant | 0.6 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.75 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.75 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.75 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.6 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.6 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.6 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.5 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.4 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.4 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.29 |
ccsA | 620184 | c.294C>A | synonymous_variant | 0.25 |
ccsA | 620225 | p.Glu112Gly | missense_variant | 0.25 |
ccsA | 620424 | c.534G>C | synonymous_variant | 0.18 |
rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
rpoB | 760757 | c.951T>C | synonymous_variant | 1.0 |
rpoB | 760759 | p.Val318Ala | missense_variant | 1.0 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.5 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.5 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.5 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.33 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.33 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.67 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.67 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.67 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.67 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.67 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.67 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.75 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.75 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.75 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.6 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 1.0 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 1.0 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.67 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.67 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.67 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.75 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.75 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.67 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.67 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.33 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.5 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.5 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.5 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.5 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.67 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.67 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.43 |
rpoB | 762197 | c.2391C>T | synonymous_variant | 0.33 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.5 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.5 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.5 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.5 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.5 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.4 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.4 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.5 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.67 |
rpoC | 762926 | c.-444C>T | upstream_gene_variant | 0.67 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.67 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.88 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.88 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.57 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.75 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.75 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.6 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.6 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.67 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.6 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.67 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.8 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.6 |
rpoC | 764172 | p.Phe268Tyr | missense_variant | 0.4 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.29 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.25 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.25 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.33 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.5 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.6 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.6 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.43 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.5 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.5 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.6 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.6 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.6 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.5 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.5 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.8 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.57 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.57 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.57 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.5 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.44 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.29 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.29 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.15 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.18 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.22 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.33 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.33 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.42 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.33 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.4 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.3 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.22 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.33 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.43 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.33 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.33 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777085 | p.Asn466Asp | missense_variant | 0.22 |
mmpL5 | 777095 | c.1386T>C | synonymous_variant | 0.22 |
mmpL5 | 777101 | c.1380C>G | synonymous_variant | 0.18 |
mmpL5 | 777110 | c.1371T>G | synonymous_variant | 0.17 |
mmpL5 | 777115 | p.Met456Leu | missense_variant | 0.18 |
mmpL5 | 777116 | c.1365C>T | synonymous_variant | 0.18 |
mmpL5 | 777133 | p.Val450Ile | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781608 | p.Ser17Gly | missense_variant | 0.25 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.67 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.75 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.67 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.33 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.33 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.75 |
rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.15 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.15 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.15 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.2 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.22 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.22 |
rplC | 801195 | c.387G>C | synonymous_variant | 0.33 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.33 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.4 |
rplC | 801249 | c.441T>C | synonymous_variant | 0.4 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.5 |
rplC | 801264 | c.456C>T | synonymous_variant | 0.5 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.5 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.5 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.5 |
rplC | 801279 | c.471G>C | synonymous_variant | 0.5 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.5 |
rplC | 801285 | c.477G>C | synonymous_variant | 0.29 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.25 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.29 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.29 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.4 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.33 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.33 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.33 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.33 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.33 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.22 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.25 |
fbiC | 1303641 | c.711C>T | synonymous_variant | 0.25 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.6 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.67 |
fbiC | 1303797 | c.867A>G | synonymous_variant | 0.4 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.5 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.6 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.5 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.5 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.5 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.5 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
fbiC | 1304711 | p.Ala594Glu | missense_variant | 1.0 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
fbiC | 1304739 | c.1809C>T | synonymous_variant | 1.0 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.6 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.6 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.5 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.5 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.5 |
fbiC | 1305372 | c.2442G>A | synonymous_variant | 0.4 |
fbiC | 1305384 | c.2454G>C | synonymous_variant | 0.5 |
fbiC | 1305396 | c.2466C>G | synonymous_variant | 0.5 |
fbiC | 1305405 | c.2475A>G | synonymous_variant | 0.4 |
fbiC | 1305417 | c.2487C>G | synonymous_variant | 0.5 |
Rv1258c | 1407538 | c.-199delC | upstream_gene_variant | 0.2 |
embR | 1417513 | c.-166A>T | upstream_gene_variant | 0.2 |
atpE | 1461206 | p.Phe54Leu | missense_variant | 0.29 |
rrs | 1471749 | n.-97C>T | upstream_gene_variant | 0.67 |
fabG1 | 1673327 | c.-113A>G | upstream_gene_variant | 0.29 |
inhA | 1674896 | p.Met232Thr | missense_variant | 0.25 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.5 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.5 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.6 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.75 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.71 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.71 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.43 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.5 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.33 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.38 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.29 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.33 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.33 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.2 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918389 | c.450G>C | synonymous_variant | 0.21 |
tlyA | 1918392 | c.453A>C | synonymous_variant | 0.21 |
tlyA | 1918422 | c.483T>C | synonymous_variant | 0.27 |
tlyA | 1918425 | c.486C>A | synonymous_variant | 0.27 |
tlyA | 1918434 | c.495C>G | synonymous_variant | 0.2 |
tlyA | 1918442 | p.Val168Ala | missense_variant | 0.2 |
ndh | 2102218 | c.825C>A | synonymous_variant | 1.0 |
ndh | 2102227 | c.816C>T | synonymous_variant | 1.0 |
ndh | 2102230 | c.813G>C | synonymous_variant | 1.0 |
ndh | 2102233 | c.810G>A | synonymous_variant | 1.0 |
PPE35 | 2169624 | p.Gly330Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288758 | p.Gly162Ser | missense_variant | 0.4 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
folC | 2746468 | c.1131G>C | synonymous_variant | 0.25 |
folC | 2747745 | c.-147A>C | upstream_gene_variant | 0.29 |
folC | 2747751 | c.-154_-153delGCinsCG | upstream_gene_variant | 0.25 |
folC | 2747759 | c.-161T>C | upstream_gene_variant | 0.22 |
folC | 2747760 | c.-162G>T | upstream_gene_variant | 0.22 |
folC | 2747772 | c.-174C>G | upstream_gene_variant | 0.29 |
folC | 2747790 | c.-192G>C | upstream_gene_variant | 0.29 |
ribD | 2987140 | p.Val101Ala | missense_variant | 0.29 |
ribD | 2987165 | c.327A>C | synonymous_variant | 0.29 |
ribD | 2987168 | c.330C>G | synonymous_variant | 0.29 |
ribD | 2987177 | c.339A>G | synonymous_variant | 0.29 |
Rv2752c | 3065028 | p.Val388Ile | missense_variant | 0.4 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.29 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.29 |
Rv2752c | 3065052 | c.1140G>A | synonymous_variant | 0.29 |
Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.29 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.25 |
Rv2752c | 3065073 | c.1119C>G | synonymous_variant | 0.25 |
Rv2752c | 3065079 | c.1113T>C | synonymous_variant | 0.25 |
Rv2752c | 3065082 | c.1110G>C | synonymous_variant | 0.25 |
Rv2752c | 3065087 | c.1105A>C | synonymous_variant | 0.22 |
Rv2752c | 3065088 | c.1104A>G | synonymous_variant | 0.22 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.29 |
Rv2752c | 3065115 | c.1077C>A | synonymous_variant | 0.29 |
Rv2752c | 3065183 | p.Ser337Ala | missense_variant | 0.33 |
Rv2752c | 3065186 | c.1006T>C | synonymous_variant | 0.29 |
Rv2752c | 3065223 | c.969T>C | synonymous_variant | 0.38 |
Rv2752c | 3065229 | c.963G>C | synonymous_variant | 0.33 |
Rv2752c | 3065232 | c.960T>C | synonymous_variant | 0.4 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.5 |
Rv2752c | 3065262 | c.930G>A | synonymous_variant | 0.45 |
Rv2752c | 3065268 | c.924A>G | synonymous_variant | 0.4 |
Rv2752c | 3065288 | c.904T>C | synonymous_variant | 0.25 |
Rv2752c | 3065292 | c.900T>C | synonymous_variant | 0.29 |
Rv2752c | 3065295 | p.Gln299Arg | missense_variant | 0.29 |
Rv2752c | 3065298 | p.Asp298Glu | missense_variant | 0.33 |
Rv2752c | 3065306 | p.Ala296Pro | missense_variant | 0.33 |
Rv2752c | 3065311 | p.Thr294Met | missense_variant | 0.33 |
Rv2752c | 3065313 | c.879A>G | synonymous_variant | 0.33 |
Rv2752c | 3065323 | p.Ala290Gly | missense_variant | 0.33 |
Rv2752c | 3065675 | p.Phe173Leu | missense_variant | 0.29 |
Rv2752c | 3066102 | c.90C>T | synonymous_variant | 0.22 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.25 |
Rv2752c | 3066150 | c.42C>A | synonymous_variant | 0.29 |
Rv2752c | 3066153 | p.Ser13Thr | missense_variant | 0.29 |
Rv2752c | 3066158 | p.Thr12Ala | missense_variant | 0.33 |
Rv2752c | 3066161 | c.31C>T | synonymous_variant | 0.33 |
Rv2752c | 3066162 | c.30C>G | synonymous_variant | 0.33 |
Rv2752c | 3066165 | c.27T>C | synonymous_variant | 0.33 |
Rv2752c | 3066176 | p.Pro6Ala | missense_variant | 0.33 |
Rv2752c | 3066177 | c.15T>C | synonymous_variant | 0.33 |
Rv2752c | 3066270 | c.-79G>A | upstream_gene_variant | 0.2 |
Rv2752c | 3066276 | c.-85G>A | upstream_gene_variant | 0.22 |
Rv2752c | 3066287 | c.-96G>C | upstream_gene_variant | 0.2 |
Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 0.17 |
Rv2752c | 3066291 | c.-100G>A | upstream_gene_variant | 0.17 |
Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 0.2 |
Rv2752c | 3066315 | c.-124C>T | upstream_gene_variant | 0.22 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.22 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.29 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.29 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.29 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.25 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.25 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.25 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.33 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.22 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.22 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.22 |
thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.33 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.33 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.33 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.29 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.29 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.29 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.29 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.29 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.25 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.25 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.33 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.83 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.8 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.75 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.6 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.6 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.6 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.6 |
thyX | 3067935 | p.Thr4Ile | missense_variant | 0.33 |
thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 1.0 |
thyA | 3073917 | c.555C>G | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087272 | c.453A>C | synonymous_variant | 0.5 |
ald | 3087278 | p.Gln153His | missense_variant | 0.57 |
ald | 3087281 | c.462G>C | synonymous_variant | 0.67 |
ald | 3087284 | c.465C>G | synonymous_variant | 0.57 |
ald | 3087290 | c.471T>C | synonymous_variant | 0.57 |
ald | 3087305 | c.486G>C | synonymous_variant | 0.57 |
ald | 3087311 | c.492C>G | synonymous_variant | 0.57 |
ald | 3087318 | p.Glu167Lys | missense_variant | 0.57 |
ald | 3087344 | c.525C>G | synonymous_variant | 0.67 |
ald | 3087347 | c.528C>G | synonymous_variant | 0.57 |
ald | 3087356 | c.537C>G | synonymous_variant | 0.57 |
ald | 3087704 | c.885T>C | synonymous_variant | 0.33 |
ald | 3087716 | c.897G>C | synonymous_variant | 0.4 |
ald | 3087726 | p.Ala303Ser | missense_variant | 0.4 |
ald | 3087729 | p.Ser304Ala | missense_variant | 0.4 |
ald | 3087737 | c.918G>C | synonymous_variant | 0.5 |
ald | 3087749 | c.930C>G | synonymous_variant | 0.4 |
ald | 3087750 | p.Tyr311Val | missense_variant | 0.4 |
ald | 3087761 | c.942C>G | synonymous_variant | 0.29 |
ald | 3087770 | c.951G>C | synonymous_variant | 0.29 |
Rv3083 | 3448759 | p.Ala86Thr | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612988 | c.128delT | frameshift_variant | 0.25 |
Rv3236c | 3613073 | p.Leu15Ser | missense_variant | 0.25 |
fbiA | 3640347 | c.-196A>G | upstream_gene_variant | 0.2 |
fbiA | 3640349 | c.-194A>G | upstream_gene_variant | 0.2 |
fbiA | 3640350 | c.-193C>T | upstream_gene_variant | 0.2 |
fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 0.25 |
fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 0.4 |
fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 0.4 |
fbiA | 3640871 | p.Ala110Gly | missense_variant | 0.4 |
fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 0.5 |
fbiB | 3640899 | c.-636G>C | upstream_gene_variant | 0.4 |
fbiA | 3640900 | p.Gln120Asn | missense_variant | 0.4 |
fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 0.4 |
fbiA | 3640930 | p.Glu130Lys | missense_variant | 0.22 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
alr | 3840995 | p.Leu142Phe | missense_variant | 0.29 |
alr | 3841059 | p.Gly121Ala | missense_variant | 0.25 |
alr | 3841304 | p.Met39Ile | missense_variant | 0.22 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.33 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.6 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.6 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.75 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.67 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.4 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.33 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.4 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.43 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.43 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.43 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.5 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.43 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.43 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.38 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.25 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.2 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.67 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.67 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.67 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.67 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 1.0 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 1.0 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 1.0 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 1.0 |
clpC1 | 4038212 | c.2493T>C | synonymous_variant | 0.4 |
clpC1 | 4038239 | c.2466T>C | synonymous_variant | 0.4 |
clpC1 | 4038255 | p.Val817Lys | missense_variant | 0.5 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 1.0 |
clpC1 | 4038272 | p.Gly811Ser | missense_variant | 1.0 |
clpC1 | 4038275 | c.2430A>G | synonymous_variant | 1.0 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.75 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.75 |
clpC1 | 4038308 | c.2397G>T | synonymous_variant | 0.5 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.4 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.29 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.5 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.5 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.5 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.3 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.58 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.78 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.7 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.7 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.67 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.75 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.67 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.67 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.67 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.67 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.67 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.67 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.5 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.6 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.67 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.86 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.5 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.5 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.5 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.5 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.5 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.6 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.6 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.6 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.6 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.5 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.5 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.29 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.29 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.33 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.75 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.75 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.75 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.75 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.75 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.75 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.67 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.67 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.8 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.8 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.5 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.5 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.57 |
embC | 4240867 | c.1005T>C | synonymous_variant | 0.18 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.18 |
embC | 4240873 | c.1011C>G | synonymous_variant | 0.18 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.2 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.18 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.17 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embC | 4240898 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.18 |
embC | 4240903 | c.1041C>G | synonymous_variant | 0.18 |
embC | 4240911 | p.Ala350Val | missense_variant | 0.2 |
embC | 4240921 | c.1059C>G | synonymous_variant | 0.25 |
embC | 4240924 | c.1062C>G | synonymous_variant | 0.2 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.18 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.43 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.43 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.44 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.57 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.5 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.5 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.5 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.5 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.4 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.4 |
embC | 4241521 | c.1659T>C | synonymous_variant | 0.33 |
embC | 4241530 | c.1668C>A | synonymous_variant | 0.33 |
embC | 4241536 | c.1674A>G | synonymous_variant | 0.21 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242764 | p.Val968Leu | missense_variant | 0.15 |
embC | 4242779 | p.Asn973Asp | missense_variant | 0.15 |
embC | 4242791 | p.Ala977Ser | missense_variant | 0.15 |
embA | 4242796 | c.-437G>C | upstream_gene_variant | 0.15 |
embA | 4242799 | c.-434T>C | upstream_gene_variant | 0.15 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.85 |
embA | 4245009 | p.Ala593Ser | missense_variant | 0.2 |
embA | 4245053 | c.1821G>C | synonymous_variant | 0.25 |
embA | 4245060 | c.1828T>C | synonymous_variant | 0.4 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.67 |
embA | 4245089 | c.1857G>C | synonymous_variant | 1.0 |
embA | 4245092 | c.1860C>G | synonymous_variant | 1.0 |
embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.67 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.67 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.67 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.67 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.67 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.4 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.4 |
embA | 4245323 | p.Met697Ile | missense_variant | 0.5 |
embA | 4245885 | p.Asp885Thr | missense_variant | 0.75 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.75 |
embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.6 |
embA | 4245927 | p.Thr899Ala | missense_variant | 0.33 |
embA | 4245930 | p.Gly900Arg | missense_variant | 0.5 |
embA | 4246264 | p.His1011Arg | missense_variant | 0.33 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.33 |
embA | 4246305 | p.Ser1025Glu | missense_variant | 0.4 |
embA | 4246308 | p.Thr1026Ala | missense_variant | 0.4 |
embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.4 |
embB | 4246319 | c.-195G>C | upstream_gene_variant | 0.4 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.67 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.5 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.67 |
embB | 4248373 | c.1860C>G | synonymous_variant | 0.33 |
embB | 4248386 | c.1873C>A | synonymous_variant | 0.33 |
embB | 4248407 | p.Leu632Val | missense_variant | 0.22 |
embB | 4248410 | p.Phe633Leu | missense_variant | 0.22 |
embB | 4248419 | p.Leu636Met | missense_variant | 0.33 |
embB | 4248425 | c.1912T>C | synonymous_variant | 0.33 |
embB | 4248430 | c.1917T>C | synonymous_variant | 0.33 |
embB | 4248432 | p.Trp640Phe | missense_variant | 0.33 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.43 |
embB | 4249095 | p.Ala861Val | missense_variant | 0.5 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4267503 | p.Thr445Asn | missense_variant | 0.33 |
aftB | 4267518 | p.Thr440Lys | missense_variant | 0.29 |
aftB | 4268112 | p.Ala242Asp | missense_variant | 0.33 |
aftB | 4268144 | c.693T>C | synonymous_variant | 0.29 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.75 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.75 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.75 |
aftB | 4269242 | c.-406C>T | upstream_gene_variant | 0.75 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.75 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.75 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 1.0 |
ubiA | 4269475 | p.Leu120Gln | missense_variant | 0.2 |
ubiA | 4269906 | c.-73G>C | upstream_gene_variant | 0.25 |
ethA | 4328449 | c.-976C>G | upstream_gene_variant | 0.25 |
ethA | 4328463 | c.-990G>C | upstream_gene_variant | 0.2 |
ethA | 4328467 | c.-994G>T | upstream_gene_variant | 0.2 |
ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 0.17 |
whiB6 | 4338498 | p.Glu8Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407905 | p.Phe100Ile | missense_variant | 0.5 |