Run ID: SRR13861413
Sample name:
Date: 03-04-2023 09:31:09
Number of reads: 233548
Percentage reads mapped: 5.84
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5532 | c.295dupG | frameshift_variant | 1.0 |
gyrB | 5832 | p.Ala198Gly | missense_variant | 1.0 |
gyrB | 6209 | c.970C>T | synonymous_variant | 0.17 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.17 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.21 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.21 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.14 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.14 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.14 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.14 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.14 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.14 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.14 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.14 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.15 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.15 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.29 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.22 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.33 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.33 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.33 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.25 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.25 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.25 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.22 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.2 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.22 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.22 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.22 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.22 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.22 |
gyrA | 8779 | p.Asp493Ala | missense_variant | 0.22 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.22 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.33 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.25 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.29 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.29 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.4 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.4 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.33 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.29 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.29 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.29 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.29 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.29 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.33 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.33 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.33 |
fgd1 | 491085 | c.303T>C | synonymous_variant | 0.12 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.14 |
fgd1 | 491094 | c.312C>G | synonymous_variant | 0.15 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.14 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.21 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.23 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.23 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.33 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.36 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.25 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.25 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.27 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.27 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.33 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.33 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.5 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.43 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.5 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.44 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.38 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.38 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.38 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.38 |
fgd1 | 491301 | c.519C>T | synonymous_variant | 0.38 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.25 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.25 |
fgd1 | 491343 | c.561C>G | synonymous_variant | 0.33 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.33 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.18 |
mshA | 575629 | c.282A>C | synonymous_variant | 0.18 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.18 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.18 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.18 |
mshA | 575648 | p.Val101Gln | missense_variant | 0.17 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.14 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.13 |
ccsA | 619735 | c.-156G>C | upstream_gene_variant | 1.0 |
ccsA | 620100 | c.210G>T | synonymous_variant | 1.0 |
rpoB | 759609 | c.-198C>A | upstream_gene_variant | 1.0 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.2 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.18 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.2 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.17 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.18 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.22 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.15 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.2 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.2 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.2 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.22 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.33 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.2 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.18 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.2 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.2 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.22 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.22 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.2 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.2 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.22 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.22 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.22 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.22 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.25 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.22 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.22 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.22 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.22 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.2 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.22 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.18 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.2 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.18 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.18 |
rpoB | 761094 | c.1288C>T | synonymous_variant | 0.18 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.18 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.18 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.18 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.22 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.17 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.15 |
rpoB | 761534 | c.1728G>A | synonymous_variant | 0.15 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.17 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.17 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.17 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.18 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.18 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.18 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.18 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.25 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.25 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.27 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.23 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.25 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.23 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.23 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.23 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.25 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.27 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.27 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.27 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.27 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.22 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.22 |
rpoB | 761815 | p.Ala670Glu | missense_variant | 0.2 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.25 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.22 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.22 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.22 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.22 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.22 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.22 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.22 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.22 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.22 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.22 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.2 |
rpoC | 762509 | c.-861T>A | upstream_gene_variant | 0.2 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.2 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.22 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.2 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.2 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.2 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.29 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.25 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.25 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.25 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.25 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.25 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 0.71 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.29 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.33 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.3 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.27 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.27 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.27 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.3 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.25 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.31 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.31 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.27 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.3 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.31 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.23 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.23 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.25 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.18 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.15 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.14 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.18 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.18 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.2 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.44 |
rpoC | 764720 | c.1351C>T | synonymous_variant | 0.44 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.5 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.5 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.43 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.29 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.29 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.29 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.38 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.38 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.43 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.38 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.3 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.4 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.44 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.38 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.33 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.22 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 0.25 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.17 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.17 |
rpoC | 766327 | c.2958C>G | synonymous_variant | 0.18 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.17 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.17 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.17 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.27 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.29 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.29 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.29 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.36 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.27 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.27 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.27 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.25 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.25 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.27 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.2 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.22 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.27 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.27 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.25 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.25 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.25 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.25 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.25 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.22 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.25 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.22 |
mmpL5 | 776796 | p.Val562Ala | missense_variant | 1.0 |
mmpS5 | 778642 | p.Trp88* | stop_gained | 1.0 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.17 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.17 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.18 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.18 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.27 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.27 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.2 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.22 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.22 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.22 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.22 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.22 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.2 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.2 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.2 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.25 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.25 |
fbiC | 1304469 | c.1539G>A | synonymous_variant | 0.2 |
fbiC | 1304499 | c.1569T>G | synonymous_variant | 0.18 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.18 |
fbiC | 1304520 | c.1590A>C | synonymous_variant | 0.18 |
fbiC | 1304523 | c.1593G>T | synonymous_variant | 0.17 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.18 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.17 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.17 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.17 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.17 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.15 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.15 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.15 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.23 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.23 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.15 |
fbiC | 1304670 | c.1740G>T | synonymous_variant | 0.17 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 0.18 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 0.17 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.2 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.3 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.2 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.2 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.22 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.22 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.25 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.25 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.25 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.29 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.38 |
Rv1258c | 1407009 | p.Ala111Asp | missense_variant | 1.0 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.15 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.15 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.13 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.15 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.17 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.18 |
atpE | 1461189 | c.145C>T | synonymous_variant | 0.17 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.17 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.17 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.2 |
atpE | 1461224 | c.180T>C | synonymous_variant | 0.18 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.15 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.33 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.22 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.22 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.25 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.22 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.2 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.22 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.29 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.25 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.25 |
inhA | 1674891 | p.Trp230Cys | missense_variant | 0.89 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.17 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.18 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.25 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.22 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.25 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.29 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.22 |
tlyA | 1918625 | p.Pro229Leu | missense_variant | 1.0 |
PPE35 | 2168838 | p.Pro592Leu | missense_variant | 0.5 |
Rv1979c | 2222721 | c.444G>C | synonymous_variant | 1.0 |
ahpC | 2726345 | p.Phe51Leu | missense_variant | 1.0 |
Rv2752c | 3064883 | p.Ser437Cys | missense_variant | 0.33 |
Rv2752c | 3067095 | c.-904G>C | upstream_gene_variant | 1.0 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.17 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.17 |
Rv3083 | 3448912 | p.Ile137Phe | missense_variant | 1.0 |
fprA | 3474088 | p.Thr28Ala | missense_variant | 0.22 |
fprA | 3474133 | p.Pro43Thr | missense_variant | 0.9 |
whiB7 | 3568676 | p.Ser2Ala | missense_variant | 1.0 |
alr | 3840783 | c.637_638insT | frameshift_variant | 1.0 |
rpoA | 3877482 | c.1026C>G | synonymous_variant | 0.25 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.25 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.25 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.25 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.25 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.18 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.2 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.22 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.22 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.22 |
rpoA | 3877677 | p.Ala277Ser | missense_variant | 0.25 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.25 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.25 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.25 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.22 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.29 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.29 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.29 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.29 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.22 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.22 |
clpC1 | 4038326 | p.Glu793Asp | missense_variant | 1.0 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.25 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.25 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.22 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.2 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.22 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.2 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.2 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.2 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.22 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.22 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.3 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.3 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.25 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.25 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.25 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.22 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.22 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.25 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.29 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.17 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.17 |
panD | 4044162 | c.120A>G | synonymous_variant | 0.17 |
embC | 4240578 | p.Ala239Val | missense_variant | 0.14 |
embC | 4240591 | c.729C>G | synonymous_variant | 0.15 |
embC | 4240594 | c.732C>G | synonymous_variant | 0.15 |
embC | 4240600 | c.738G>C | synonymous_variant | 0.15 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.18 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.17 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.17 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.2 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.2 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.18 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.2 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.2 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.2 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.25 |
embC | 4241026 | c.1164C>G | synonymous_variant | 1.0 |
embA | 4242250 | c.-983C>G | upstream_gene_variant | 1.0 |
embA | 4245388 | p.Ala719Gly | missense_variant | 0.25 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.4 |
embB | 4247398 | c.885G>T | synonymous_variant | 1.0 |
embB | 4249328 | p.Met939Leu | missense_variant | 1.0 |
aftB | 4267490 | c.1347G>C | synonymous_variant | 1.0 |
ethA | 4326203 | p.Ser424* | stop_gained | 1.0 |