Run ID: ERR4817998
Sample name:
Date: 01-04-2023 15:18:42
Number of reads: 3041318
Percentage reads mapped: 74.14
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.48 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6157 | c.918C>T | synonymous_variant | 0.24 |
gyrB | 6184 | c.945C>G | synonymous_variant | 0.17 |
gyrB | 6196 | c.957C>A | synonymous_variant | 0.17 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.19 |
gyrB | 6211 | c.972G>C | synonymous_variant | 0.18 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.18 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.18 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.12 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.12 |
gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.12 |
gyrB | 6590 | p.Arg451Ser | missense_variant | 0.13 |
gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.13 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.18 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.19 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.19 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.13 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.12 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.13 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.17 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.16 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.15 |
gyrA | 6703 | c.-599G>T | upstream_gene_variant | 0.16 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.15 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.15 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.16 |
gyrA | 6715 | c.-587C>T | upstream_gene_variant | 0.17 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.15 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.15 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.2 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.16 |
gyrA | 6764 | c.-538C>T | upstream_gene_variant | 0.15 |
gyrA | 6772 | c.-530C>G | upstream_gene_variant | 0.15 |
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 0.15 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.15 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.14 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.15 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.16 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.11 |
gyrA | 7120 | c.-182T>C | upstream_gene_variant | 0.16 |
gyrA | 7129 | c.-173T>G | upstream_gene_variant | 0.16 |
gyrA | 7136 | c.-166T>C | upstream_gene_variant | 0.21 |
gyrA | 7144 | c.-158A>G | upstream_gene_variant | 0.26 |
gyrA | 7150 | c.-152G>A | upstream_gene_variant | 0.28 |
gyrA | 7153 | c.-149G>C | upstream_gene_variant | 0.29 |
gyrA | 7159 | c.-143C>T | upstream_gene_variant | 0.3 |
gyrA | 7162 | c.-140C>G | upstream_gene_variant | 0.29 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.32 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.27 |
gyrA | 7186 | c.-116C>G | upstream_gene_variant | 0.21 |
gyrA | 7189 | c.-113C>T | upstream_gene_variant | 0.19 |
gyrB | 7210 | p.Asp657Glu | missense_variant | 0.15 |
gyrA | 7216 | c.-86G>C | upstream_gene_variant | 0.16 |
gyrA | 7225 | c.-77T>C | upstream_gene_variant | 0.15 |
gyrA | 7355 | c.54T>A | synonymous_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.14 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.15 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.15 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.16 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.14 |
gyrA | 7421 | c.120G>T | synonymous_variant | 0.14 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.16 |
gyrA | 7430 | c.129G>A | synonymous_variant | 0.16 |
gyrA | 7439 | c.138C>T | synonymous_variant | 0.16 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.16 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.14 |
gyrA | 7466 | c.165G>C | synonymous_variant | 0.12 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.11 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.12 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.18 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.18 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.22 |
gyrA | 7496 | c.195C>G | synonymous_variant | 0.21 |
gyrA | 7499 | c.198G>C | synonymous_variant | 0.22 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.2 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.19 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.2 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.23 |
gyrA | 7559 | c.258G>A | synonymous_variant | 0.24 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.25 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7587 | c.286C>T | synonymous_variant | 0.15 |
gyrA | 7595 | c.294C>T | synonymous_variant | 0.14 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.14 |
gyrA | 7847 | c.546G>C | synonymous_variant | 0.15 |
gyrA | 7853 | c.552C>T | synonymous_variant | 0.15 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.16 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.15 |
gyrA | 7868 | p.Ile189Met | missense_variant | 0.15 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.16 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.15 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.14 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.14 |
gyrA | 8354 | c.1053G>C | synonymous_variant | 0.13 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.15 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.16 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.2 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.18 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.17 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.2 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.16 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.18 |
gyrA | 8993 | c.1692C>T | synonymous_variant | 0.16 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.18 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.19 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.18 |
gyrA | 9023 | c.1722A>T | synonymous_variant | 0.16 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.13 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.21 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.21 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.2 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.14 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.13 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.12 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.16 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.18 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.17 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.17 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.18 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.19 |
rpoB | 760418 | c.612G>A | synonymous_variant | 0.2 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.27 |
rpoB | 760433 | c.627C>T | synonymous_variant | 0.31 |
rpoB | 760454 | c.648C>G | synonymous_variant | 0.26 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.24 |
rpoB | 760469 | c.663C>T | synonymous_variant | 0.21 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.22 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.19 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.2 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 760487 | c.681G>C | synonymous_variant | 0.17 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.17 |
rpoB | 760508 | c.702G>A | synonymous_variant | 0.18 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.16 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.13 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.17 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.18 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.12 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.12 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.11 |
rpoB | 760869 | p.Val355Leu | missense_variant | 0.12 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.14 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.14 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.14 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.12 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.14 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.12 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.18 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.21 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.2 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.16 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.16 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.16 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.16 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.2 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.12 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.11 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.11 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.11 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.12 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.12 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.12 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.19 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.18 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.17 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.17 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.14 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.15 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.16 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.16 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.13 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.14 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.12 |
rpoB | 761760 | p.Ile652Val | missense_variant | 0.12 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.14 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.11 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.25 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.23 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.2 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.22 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.21 |
rpoB | 762299 | c.2493G>C | synonymous_variant | 0.21 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.91 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.13 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.13 |
rpoC | 762515 | c.-855C>T | upstream_gene_variant | 0.14 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.18 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.19 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.21 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.19 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.18 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.2 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.2 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.17 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.19 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.16 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.24 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.26 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.23 |
rpoC | 763076 | c.-294C>A | upstream_gene_variant | 0.23 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.28 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.28 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.23 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.2 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.2 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.16 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.14 |
rpoC | 763157 | c.-213G>T | upstream_gene_variant | 0.13 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.33 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.32 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.34 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.16 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.13 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.17 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.17 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.16 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.16 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.16 |
rpoC | 763714 | c.345G>A | synonymous_variant | 0.15 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.15 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.14 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.15 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.16 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.19 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.22 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.22 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.22 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.21 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.22 |
rpoC | 764392 | c.1023C>T | synonymous_variant | 0.23 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.22 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.19 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.15 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.15 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.15 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.13 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.12 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.17 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.17 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.15 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.21 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.24 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.25 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.25 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.24 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.2 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.2 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.19 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.19 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.22 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.24 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.28 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.25 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.23 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.25 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.25 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.26 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.25 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.24 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.24 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.24 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.22 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.18 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.13 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.16 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.14 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.13 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.13 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.14 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.14 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.14 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.14 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.12 |
rpoC | 765394 | c.2025G>A | synonymous_variant | 0.15 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.14 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.14 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.15 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.16 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.18 |
rpoC | 765449 | p.Ala694Ser | missense_variant | 0.17 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.17 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.15 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.12 |
rpoC | 765480 | p.Tyr704Phe | missense_variant | 0.12 |
rpoC | 765496 | c.2127C>T | synonymous_variant | 0.13 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.13 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.12 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.12 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.11 |
rpoC | 766624 | c.3255G>C | synonymous_variant | 0.11 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.11 |
rpoC | 766975 | c.3606C>T | synonymous_variant | 0.12 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.23 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.24 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.23 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.18 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.18 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.13 |
rpoC | 767100 | p.Lys1244Arg | missense_variant | 0.13 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.14 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.15 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.15 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.14 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.16 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.17 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.15 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.13 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.14 |
rpsL | 781877 | c.318T>A | synonymous_variant | 0.14 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.12 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.15 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 0.15 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.14 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.14 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.12 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.12 |
Rv1258c | 1407274 | p.Asp23Asn | missense_variant | 1.0 |
atpE | 1461197 | c.153A>C | synonymous_variant | 0.14 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.15 |
atpE | 1461230 | c.186G>T | synonymous_variant | 0.13 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.31 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472050 | n.205G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475220 | n.1563G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475774 | n.2117C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475953 | n.2296A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476295 | n.2638C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476665 | n.3008T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476684 | n.3027C>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.12 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.12 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.12 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.13 |
rpsA | 1833616 | c.75A>T | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.16 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.12 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.13 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.24 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.18 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.18 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.18 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.2 |
rpsA | 1833751 | c.210C>T | synonymous_variant | 0.22 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.22 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.26 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.26 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.19 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.2 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.25 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.27 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.25 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.27 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.33 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.31 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.32 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.28 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.26 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.26 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.27 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.22 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.16 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.25 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.25 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.25 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.25 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.26 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.28 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.3 |
rpsA | 1834073 | p.Lys178Arg | missense_variant | 0.29 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.18 |
rpsA | 1834228 | c.687C>A | synonymous_variant | 0.2 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.19 |
rpsA | 1834234 | c.693G>T | synonymous_variant | 0.21 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.21 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.22 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.23 |
rpsA | 1834252 | c.711C>G | synonymous_variant | 0.21 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.23 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.24 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.25 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.24 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.19 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.16 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.16 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.13 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.12 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.16 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.17 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.14 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.13 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726636 | c.444G>C | synonymous_variant | 0.12 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.13 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.14 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.16 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.16 |
ahpC | 2726678 | c.486G>C | synonymous_variant | 0.16 |
ahpC | 2726681 | c.489A>C | synonymous_variant | 0.17 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.16 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.15 |
ahpC | 2726717 | c.525A>C | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.11 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.12 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.12 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.16 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.18 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.16 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.15 |
rpoA | 3877860 | c.648C>T | synonymous_variant | 0.16 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.19 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.18 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.15 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.12 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.14 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.15 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.14 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.15 |
rpoA | 3878079 | c.429C>T | synonymous_variant | 0.16 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.16 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.17 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.17 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.16 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.18 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.21 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.2 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.21 |
rpoA | 3878175 | c.333G>T | synonymous_variant | 0.2 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.18 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.18 |
rpoA | 3878205 | c.303T>A | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.19 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.16 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878274 | c.234G>C | synonymous_variant | 0.15 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.18 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.18 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.18 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.13 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.12 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.12 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.12 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.12 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.12 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.12 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.12 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.25 |
clpC1 | 4038584 | c.2121G>T | synonymous_variant | 0.13 |
clpC1 | 4038587 | c.2118C>G | synonymous_variant | 0.13 |
clpC1 | 4038602 | c.2103G>C | synonymous_variant | 0.11 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.11 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.2 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.2 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.22 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.23 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.24 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.29 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.27 |
clpC1 | 4039100 | c.1605C>G | synonymous_variant | 0.13 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.12 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.13 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.14 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.13 |
clpC1 | 4039136 | c.1569C>T | synonymous_variant | 0.19 |
clpC1 | 4039139 | c.1566G>A | synonymous_variant | 0.19 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.19 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.2 |
clpC1 | 4039166 | c.1539G>A | synonymous_variant | 0.21 |
clpC1 | 4039169 | c.1536A>G | synonymous_variant | 0.21 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.2 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.23 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.23 |
clpC1 | 4039190 | c.1515C>T | synonymous_variant | 0.24 |
clpC1 | 4039196 | c.1509G>A | synonymous_variant | 0.19 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.16 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.17 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.27 |
clpC1 | 4039265 | c.1440C>T | synonymous_variant | 0.25 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.22 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.22 |
clpC1 | 4039280 | c.1425G>T | synonymous_variant | 0.22 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.2 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.22 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.25 |
clpC1 | 4039316 | p.Glu463Asp | missense_variant | 0.18 |
clpC1 | 4039319 | c.1386T>A | synonymous_variant | 0.14 |
clpC1 | 4039322 | c.1383T>G | synonymous_variant | 0.14 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.13 |
clpC1 | 4039360 | p.Ser449Arg | missense_variant | 0.13 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.12 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.19 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.18 |
clpC1 | 4039451 | c.1254G>A | synonymous_variant | 0.12 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.12 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.22 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.21 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.28 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.27 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.31 |
clpC1 | 4039649 | c.1056G>T | synonymous_variant | 0.35 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.39 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.46 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.47 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.45 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.46 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.4 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.41 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.34 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.31 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.28 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.28 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.28 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.27 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.26 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.27 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.2 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.19 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.16 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.16 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.19 |
clpC1 | 4039844 | c.861C>T | synonymous_variant | 0.23 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.25 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.27 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.25 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.24 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.18 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.16 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.16 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.12 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.14 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.2 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.21 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.2 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.21 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.2 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.21 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.21 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.21 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.22 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.25 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.23 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.16 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.16 |
clpC1 | 4040126 | c.579C>T | synonymous_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326090 | c.1384C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |