Run ID: SRR8692879
Sample name:
Date: 13-08-2023 19:42:48
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.4 | linezolid |
katG | 2154391 | p.Ala574Glu | missense_variant | 0.13 | isoniazid |
katG | 2155181 | p.Asp311Tyr | missense_variant | 0.18 | isoniazid |
pncA | 2289162 | p.Leu27Pro | missense_variant | 0.18 | pyrazinamide |
embB | 4247231 | p.Asp240His | missense_variant | 0.22 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5926 | c.687G>T | synonymous_variant | 0.22 |
gyrB | 6912 | p.Asn558Ile | missense_variant | 0.17 |
gyrB | 7265 | c.2026T>C | stop_lost&splice_region_variant | 0.12 |
gyrA | 7397 | c.96G>A | synonymous_variant | 0.2 |
gyrA | 7571 | c.270G>T | synonymous_variant | 0.17 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.11 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.12 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.13 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.15 |
gyrA | 7874 | c.573G>T | synonymous_variant | 0.25 |
gyrA | 8550 | p.Ala417Ser | missense_variant | 0.2 |
gyrA | 8602 | p.Ala434Val | missense_variant | 0.14 |
gyrA | 9286 | p.Ala662Glu | missense_variant | 0.14 |
gyrA | 9375 | p.Pro692Thr | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.36 |
mshA | 575690 | p.Gly115Arg | missense_variant | 0.4 |
mshA | 576200 | p.Arg285Ser | missense_variant | 0.22 |
mshA | 576247 | c.900A>G | synonymous_variant | 0.4 |
mshA | 576391 | c.1044G>T | synonymous_variant | 0.4 |
mshA | 576789 | c.1442G>T | stop_lost&splice_region_variant | 0.2 |
rpoB | 759989 | c.183G>T | synonymous_variant | 0.15 |
rpoB | 760643 | p.Glu279Asp | missense_variant | 0.22 |
rpoB | 760694 | p.Lys296Asn | missense_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.11 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.12 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.14 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.14 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.14 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.2 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.2 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.14 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.14 |
rpoB | 761408 | c.1602G>T | synonymous_variant | 0.18 |
rpoB | 761918 | p.Asp704Glu | missense_variant | 0.14 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.22 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.2 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.17 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.14 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.14 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.15 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.15 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.19 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.18 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.17 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.22 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.24 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.27 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.27 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.25 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.25 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.14 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.13 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.13 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.12 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.12 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.17 |
rpoB | 763106 | p.Ile1100Met | missense_variant | 0.14 |
rpoC | 763375 | c.6C>A | synonymous_variant | 0.17 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.28 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.29 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.31 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.29 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.26 |
rpoC | 763443 | p.Tyr25Phe | missense_variant | 0.28 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.3 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.3 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.33 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.3 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.19 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.17 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.17 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.12 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.13 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.14 |
rpoC | 764322 | p.Pro318Gln | missense_variant | 0.14 |
rpoC | 764329 | c.960C>A | synonymous_variant | 0.15 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.18 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.25 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.2 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.2 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.27 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.3 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.38 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.44 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.57 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.67 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.67 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.57 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.4 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.36 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.36 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.36 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.33 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.33 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.2 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.19 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.13 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.2 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.18 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.11 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.16 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.14 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.15 |
rpoC | 764665 | c.1296C>A | synonymous_variant | 0.15 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.16 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.17 |
rpoC | 764881 | c.1512G>T | synonymous_variant | 0.33 |
rpoC | 765119 | p.Gly584Trp | missense_variant | 0.17 |
rpoC | 765728 | p.Gln787Lys | missense_variant | 0.18 |
rpoC | 765800 | p.Phe811Leu | missense_variant | 0.12 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.12 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.12 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.12 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.12 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.12 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.17 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.17 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.15 |
rpoC | 766036 | c.2667C>T | synonymous_variant | 0.2 |
rpoC | 766993 | p.Met1208Ile | missense_variant | 0.15 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.33 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.33 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.33 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.43 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.38 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.43 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.5 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.5 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.5 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.5 |
rpoC | 767186 | p.Gln1273Asn | missense_variant | 0.5 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.43 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.43 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.5 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.4 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.21 |
mmpL5 | 775684 | p.Leu933Ile | missense_variant | 0.18 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.11 |
mmpL5 | 775862 | c.2619G>C | synonymous_variant | 0.11 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.15 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.16 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.17 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.14 |
mmpL5 | 776798 | c.1683G>T | synonymous_variant | 0.25 |
mmpL5 | 776876 | p.Gln535His | missense_variant | 0.15 |
mmpL5 | 776900 | p.Asn527Lys | missense_variant | 0.15 |
mmpL5 | 777417 | p.Pro355Gln | missense_variant | 0.14 |
mmpL5 | 777434 | c.1047C>A | synonymous_variant | 0.13 |
mmpL5 | 777533 | c.948C>A | synonymous_variant | 0.18 |
mmpR5 | 778019 | c.-971C>T | upstream_gene_variant | 0.13 |
mmpL5 | 778248 | p.Ile78Thr | missense_variant | 0.13 |
mmpR5 | 779332 | p.Gln115Lys | missense_variant | 0.25 |
mmpS5 | 779662 | c.-757G>T | upstream_gene_variant | 0.14 |
rplC | 800757 | c.-52G>T | upstream_gene_variant | 0.33 |
rplC | 800873 | p.Arg22Lys | missense_variant | 0.13 |
rplC | 801409 | p.Arg201Ser | missense_variant | 0.14 |
fbiC | 1304036 | p.Arg369Leu | missense_variant | 0.18 |
fbiC | 1304058 | p.Glu376Asp | missense_variant | 0.15 |
fbiC | 1304243 | p.Pro438His | missense_variant | 0.29 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.13 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.14 |
fbiC | 1304727 | c.1797A>C | synonymous_variant | 0.14 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.12 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.12 |
fbiC | 1304751 | c.1821C>G | synonymous_variant | 0.13 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.12 |
fbiC | 1304769 | c.1839C>G | synonymous_variant | 0.11 |
fbiC | 1304978 | p.Gly683Val | missense_variant | 0.4 |
fbiC | 1305208 | p.Gly760Cys | missense_variant | 0.29 |
Rv1258c | 1406414 | c.927G>T | synonymous_variant | 0.14 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.67 |
Rv1258c | 1406727 | p.Pro205Leu | missense_variant | 0.18 |
Rv1258c | 1407342 | c.-2T>C | upstream_gene_variant | 0.22 |
atpE | 1461279 | p.Pro79Thr | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472502 | n.657G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473292 | n.1447G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473601 | n.-57C>A | upstream_gene_variant | 0.15 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474452 | n.795C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474524 | n.867C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474775 | n.1118G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474810 | n.1153G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475235 | n.1578C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475255 | n.1598C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475562 | n.1905C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475640 | n.1983G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475860 | n.2203C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476189 | n.2532C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476476 | n.2819G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.2 |
inhA | 1673454 | c.-748C>A | upstream_gene_variant | 0.25 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.17 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.18 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.18 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.18 |
inhA | 1674804 | c.603G>C | synonymous_variant | 0.18 |
inhA | 1674810 | c.609C>G | synonymous_variant | 0.17 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.13 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.13 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.12 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.12 |
rpsA | 1834167 | p.Gly209Val | missense_variant | 0.17 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.12 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.12 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.15 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.15 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.12 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.12 |
rpsA | 1834849 | c.1308C>T | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.22 |
tlyA | 1918660 | p.Leu241Met | missense_variant | 0.22 |
ndh | 2102281 | c.762C>A | synonymous_variant | 0.2 |
ndh | 2102563 | c.480G>T | synonymous_variant | 0.14 |
ndh | 2102611 | c.432G>C | synonymous_variant | 0.12 |
katG | 2154946 | p.Ile389Thr | missense_variant | 0.17 |
katG | 2156050 | p.Pro21His | missense_variant | 0.18 |
katG | 2156139 | c.-28G>T | upstream_gene_variant | 0.14 |
katG | 2156162 | c.-51G>T | upstream_gene_variant | 0.15 |
katG | 2156276 | c.-165C>A | upstream_gene_variant | 0.15 |
PPE35 | 2167939 | p.Ala892Thr | missense_variant | 0.22 |
PPE35 | 2167941 | p.Ser891Thr | missense_variant | 0.22 |
PPE35 | 2168876 | p.Phe579Leu | missense_variant | 0.2 |
PPE35 | 2168977 | p.Ala546Ser | missense_variant | 0.17 |
Rv1979c | 2222184 | p.Trp327Cys | missense_variant | 0.18 |
Rv1979c | 2222450 | p.Ala239Ser | missense_variant | 0.13 |
Rv1979c | 2222697 | p.Asn156Lys | missense_variant | 0.18 |
Rv1979c | 2222772 | p.Glu131Asp | missense_variant | 0.13 |
Rv1979c | 2222862 | c.303C>A | synonymous_variant | 0.18 |
Rv1979c | 2222899 | p.Arg89Gln | missense_variant | 0.22 |
Rv1979c | 2223078 | c.87C>A | synonymous_variant | 0.29 |
pncA | 2288854 | p.Val130Leu | missense_variant | 0.33 |
pncA | 2289527 | c.-286C>G | upstream_gene_variant | 0.14 |
pncA | 2290038 | c.-797G>T | upstream_gene_variant | 0.17 |
eis | 2714192 | p.Gln381Lys | missense_variant | 0.17 |
eis | 2714375 | p.Val320Phe | missense_variant | 0.17 |
eis | 2714653 | p.Arg227Leu | missense_variant | 0.17 |
eis | 2714660 | p.Leu225Val | missense_variant | 0.17 |
eis | 2714775 | c.558G>T | synonymous_variant | 0.17 |
eis | 2714785 | p.Arg183Leu | missense_variant | 0.18 |
eis | 2715187 | p.Arg49His | missense_variant | 0.13 |
ahpC | 2725968 | c.-225C>A | upstream_gene_variant | 0.17 |
folC | 2746276 | p.Asp441Glu | missense_variant | 0.5 |
folC | 2746879 | p.Lys240Asn | missense_variant | 0.18 |
folC | 2747628 | c.-30G>T | upstream_gene_variant | 0.14 |
ribD | 2986849 | p.Ser4Tyr | missense_variant | 0.13 |
ribD | 2987283 | p.Ala149Ser | missense_variant | 0.22 |
ribD | 2987614 | c.776G>A | splice_region_variant&stop_retained_variant | 0.15 |
Rv2752c | 3065202 | c.990T>C | synonymous_variant | 0.11 |
Rv2752c | 3065205 | c.987T>C | synonymous_variant | 0.11 |
Rv2752c | 3065223 | c.969T>C | synonymous_variant | 0.11 |
Rv2752c | 3065232 | c.960T>C | synonymous_variant | 0.12 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.11 |
Rv2752c | 3067126 | c.-935C>A | upstream_gene_variant | 0.13 |
thyX | 3067824 | p.Arg41Leu | missense_variant | 0.25 |
thyA | 3074282 | p.Arg64Ser | missense_variant | 0.13 |
thyA | 3074298 | p.Glu58Asp | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.2 |
ald | 3087874 | p.Ser352Tyr | missense_variant | 0.18 |
ald | 3087908 | p.Phe363Leu | missense_variant | 0.2 |
fbiD | 3339102 | c.-16C>A | upstream_gene_variant | 0.29 |
fbiD | 3339511 | p.Ala132Ser | missense_variant | 0.22 |
Rv3083 | 3448357 | c.-147C>A | upstream_gene_variant | 0.21 |
Rv3083 | 3449010 | p.Trp169Cys | missense_variant | 0.15 |
fprA | 3474099 | p.Asp31Glu | missense_variant | 0.15 |
fprA | 3474253 | p.Val83Phe | missense_variant | 0.18 |
fprA | 3474275 | p.Pro90His | missense_variant | 0.17 |
fprA | 3474278 | p.Gly91Val | missense_variant | 0.17 |
fprA | 3474301 | p.Ala99Ser | missense_variant | 0.18 |
fprA | 3475039 | p.Gly345Cys | missense_variant | 0.22 |
fprA | 3475342 | p.Ser446Gly | missense_variant | 0.29 |
whiB7 | 3568419 | c.261C>A | synonymous_variant | 0.17 |
Rv3236c | 3612721 | c.396G>T | synonymous_variant | 0.29 |
Rv3236c | 3612863 | p.Ser85Ile | missense_variant | 0.14 |
Rv3236c | 3613153 | c.-37G>T | upstream_gene_variant | 0.18 |
fbiA | 3640405 | c.-138G>T | upstream_gene_variant | 0.15 |
fbiA | 3640419 | c.-124G>T | upstream_gene_variant | 0.13 |
fbiB | 3641960 | c.426C>T | synonymous_variant | 0.2 |
fbiB | 3641967 | p.Ala145Ser | missense_variant | 0.18 |
alr | 3840479 | p.Tyr314* | stop_gained | 0.13 |
alr | 3841073 | c.348C>T | synonymous_variant | 0.17 |
alr | 3841098 | p.Pro108Leu | missense_variant | 0.18 |
alr | 3841161 | p.Ala87Asp | missense_variant | 0.22 |
alr | 3841458 | c.-38G>T | upstream_gene_variant | 0.15 |
alr | 3841525 | c.-105G>T | upstream_gene_variant | 0.15 |
alr | 3841612 | c.-192A>C | upstream_gene_variant | 0.17 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.15 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.15 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.15 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.15 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.15 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.21 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.25 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.21 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.21 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.23 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.23 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.25 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.21 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.2 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.13 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 0.19 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.14 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.15 |
rpoA | 3877964 | c.544C>A | synonymous_variant | 0.17 |
rpoA | 3878010 | c.498C>A | synonymous_variant | 0.18 |
rpoA | 3878360 | p.Ala50Ser | missense_variant | 0.22 |
rpoA | 3878572 | c.-65G>T | upstream_gene_variant | 0.33 |
clpC1 | 4038607 | p.Glu700* | stop_gained | 0.22 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.33 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.25 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.25 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.2 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.2 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.2 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.22 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.2 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.2 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.33 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.33 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.33 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.33 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.4 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.33 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.25 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.23 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.17 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.2 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.25 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.25 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.22 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.22 |
clpC1 | 4038852 | p.Pro618Gln | missense_variant | 0.25 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.18 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.18 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.15 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.15 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.15 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.15 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.23 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.18 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.25 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.25 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.21 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.25 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.25 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.2 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.22 |
clpC1 | 4039517 | c.1188C>A | synonymous_variant | 0.15 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.12 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.12 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.12 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.12 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.13 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.14 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.14 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.16 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.11 |
clpC1 | 4040253 | p.Ala151Asp | missense_variant | 0.18 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.12 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.11 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.13 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.14 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.13 |
clpC1 | 4040671 | p.Val12Phe | missense_variant | 0.17 |
panD | 4043966 | p.Val106Leu | missense_variant | 0.2 |
panD | 4044230 | p.Ala18Ser | missense_variant | 0.18 |
panD | 4044377 | c.-96G>T | upstream_gene_variant | 0.22 |
embC | 4239900 | p.Arg13Leu | missense_variant | 0.14 |
embC | 4239906 | p.Pro15Gln | missense_variant | 0.14 |
embC | 4240007 | p.Leu49Met | missense_variant | 0.22 |
embC | 4240238 | p.Ala126Ser | missense_variant | 0.17 |
embC | 4240247 | p.Asp129Tyr | missense_variant | 0.15 |
embC | 4240289 | p.Pro143Thr | missense_variant | 0.18 |
embC | 4240625 | p.Asp255Asn | missense_variant | 0.2 |
embC | 4241235 | p.Thr458Asn | missense_variant | 0.25 |
embC | 4242094 | p.Leu744Phe | missense_variant | 0.2 |
embC | 4242239 | p.Asp793Tyr | missense_variant | 0.18 |
embC | 4242413 | p.Leu851Met | missense_variant | 0.15 |
embC | 4243079 | p.Ala1073Thr | missense_variant | 0.25 |
embA | 4244479 | p.Thr416Lys | missense_variant | 0.15 |
embA | 4244533 | p.Thr434Asn | missense_variant | 0.13 |
embA | 4244598 | p.Leu456Met | missense_variant | 0.17 |
embA | 4245500 | p.Gln756His | missense_variant | 0.29 |
embA | 4245525 | p.Gly765Cys | missense_variant | 0.4 |
embB | 4246753 | c.240C>T | synonymous_variant | 0.25 |
embB | 4246990 | c.477C>A | synonymous_variant | 0.18 |
embB | 4247013 | p.Pro167Gln | missense_variant | 0.18 |
embB | 4247226 | p.Arg238His | missense_variant | 0.25 |
embB | 4247362 | c.849G>C | synonymous_variant | 0.29 |
embB | 4247788 | p.Tyr425* | stop_gained | 0.25 |
embB | 4247815 | c.1302C>A | synonymous_variant | 0.25 |
embB | 4248130 | c.1617G>T | synonymous_variant | 0.2 |
embB | 4249124 | p.Gly871Trp | missense_variant | 0.2 |
embB | 4249241 | c.2728C>T | synonymous_variant | 0.5 |
embB | 4249766 | p.Arg1085Cys | missense_variant | 0.14 |
aftB | 4267168 | p.Gln557Lys | missense_variant | 0.17 |
aftB | 4267974 | p.Ser288* | stop_gained | 0.17 |
aftB | 4268604 | p.Arg78Leu | missense_variant | 0.2 |
aftB | 4268630 | c.207G>T | synonymous_variant | 0.2 |
aftB | 4269072 | c.-236G>C | upstream_gene_variant | 0.12 |
aftB | 4269084 | c.-248G>C | upstream_gene_variant | 0.12 |
aftB | 4269087 | c.-251G>C | upstream_gene_variant | 0.11 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.11 |
aftB | 4269141 | c.-307_-305delTTGinsCTC | upstream_gene_variant | 0.12 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.12 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.13 |
aftB | 4269165 | c.-329G>T | upstream_gene_variant | 0.17 |
aftB | 4269171 | c.-335C>G | upstream_gene_variant | 0.17 |
aftB | 4269177 | c.-341G>C | upstream_gene_variant | 0.25 |
ubiA | 4269186 | p.Thr216Ser | missense_variant | 0.25 |
ubiA | 4269199 | p.Ser212Asn | missense_variant | 0.27 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.21 |
aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.15 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.17 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.17 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.18 |
ubiA | 4269238 | p.Ala199Val | missense_variant | 0.18 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.18 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.18 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.22 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.17 |
aftB | 4269264 | c.-428C>T | upstream_gene_variant | 0.17 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 0.17 |
aftB | 4269291 | c.-455A>G | upstream_gene_variant | 0.15 |
ubiA | 4269297 | p.Ile179Met | missense_variant | 0.14 |
ethR | 4326880 | c.-669G>T | upstream_gene_variant | 0.25 |
ethA | 4327320 | p.Gly52* | stop_gained | 0.13 |
ethA | 4328208 | c.-735G>T | upstream_gene_variant | 0.17 |
ethA | 4328470 | c.-997G>T | upstream_gene_variant | 0.27 |
whiB6 | 4338172 | c.350G>T | stop_lost&splice_region_variant | 0.2 |
whiB6 | 4338184 | p.Ala113Val | missense_variant | 0.2 |
whiB6 | 4338193 | p.Arg110Leu | missense_variant | 0.22 |
whiB6 | 4338200 | p.Asp108Tyr | missense_variant | 0.2 |
whiB6 | 4338259 | p.Arg88Leu | missense_variant | 0.18 |
gid | 4407625 | p.Ala193Glu | missense_variant | 0.2 |
gid | 4407634 | p.Thr190Lys | missense_variant | 0.2 |