Run ID: ERR4816113
Sample name:
Date: 01-04-2023 14:14:56
Number of reads: 1374700
Percentage reads mapped: 69.45
Strain: lineage4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.14 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.14 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.16 |
gyrA | 6631 | c.-671C>T | upstream_gene_variant | 0.19 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.17 |
gyrA | 6640 | c.-662A>T | upstream_gene_variant | 0.19 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.19 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.23 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.22 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.2 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.21 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.21 |
gyrA | 6697 | c.-605C>T | upstream_gene_variant | 0.26 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.26 |
gyrA | 6703 | c.-599G>T | upstream_gene_variant | 0.26 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.26 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.28 |
gyrA | 6715 | c.-587C>T | upstream_gene_variant | 0.27 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.26 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.25 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.23 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.17 |
gyrA | 6764 | c.-538C>T | upstream_gene_variant | 0.16 |
gyrA | 6772 | c.-530C>G | upstream_gene_variant | 0.14 |
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 0.13 |
gyrA | 6796 | c.-506C>T | upstream_gene_variant | 0.13 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.13 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.17 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.24 |
gyrA | 7072 | c.-230G>A | upstream_gene_variant | 0.27 |
gyrA | 7078 | c.-224A>T | upstream_gene_variant | 0.28 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.3 |
gyrA | 7090 | c.-212C>T | upstream_gene_variant | 0.29 |
gyrA | 7093 | c.-209T>C | upstream_gene_variant | 0.3 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.3 |
gyrA | 7100 | c.-202T>C | upstream_gene_variant | 0.32 |
gyrA | 7120 | c.-182T>C | upstream_gene_variant | 0.34 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.33 |
gyrA | 7126 | c.-176G>C | upstream_gene_variant | 0.31 |
gyrA | 7129 | c.-173T>G | upstream_gene_variant | 0.32 |
gyrA | 7136 | c.-166T>C | upstream_gene_variant | 0.35 |
gyrA | 7144 | c.-158A>G | upstream_gene_variant | 0.3 |
gyrA | 7150 | c.-152G>A | upstream_gene_variant | 0.32 |
gyrA | 7153 | c.-149G>C | upstream_gene_variant | 0.32 |
gyrA | 7159 | c.-143C>T | upstream_gene_variant | 0.29 |
gyrA | 7162 | c.-140C>G | upstream_gene_variant | 0.3 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.3 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.28 |
gyrA | 7186 | c.-116C>G | upstream_gene_variant | 0.22 |
gyrA | 7189 | c.-113C>T | upstream_gene_variant | 0.19 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.19 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.21 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.22 |
gyrA | 7430 | c.129G>A | synonymous_variant | 0.22 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.21 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.18 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.17 |
gyrA | 7466 | c.165G>C | synonymous_variant | 0.17 |
gyrA | 7469 | c.168C>T | synonymous_variant | 0.16 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.16 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.19 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.24 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.25 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.25 |
gyrA | 7496 | c.195C>G | synonymous_variant | 0.26 |
gyrA | 7499 | c.198G>C | synonymous_variant | 0.26 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.28 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.27 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.26 |
gyrA | 7559 | c.258G>A | synonymous_variant | 0.17 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.16 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7587 | c.286C>T | synonymous_variant | 0.15 |
gyrA | 7595 | c.294C>T | synonymous_variant | 0.15 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.15 |
gyrA | 7619 | c.318C>T | synonymous_variant | 0.15 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.14 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.22 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.16 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.15 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.14 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.16 |
gyrA | 8993 | c.1692C>T | synonymous_variant | 0.16 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.15 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.16 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.16 |
gyrA | 9023 | c.1722A>T | synonymous_variant | 0.14 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.14 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.14 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.14 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.15 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.15 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.14 |
gyrA | 9063 | p.Ser588Ala | missense_variant | 0.13 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490661 | c.-122_-121insGCGAGC | upstream_gene_variant | 0.98 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.14 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.18 |
rpoB | 760276 | p.Lys157Met | missense_variant | 0.19 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.16 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.14 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.13 |
rpoB | 760319 | p.Ser171Arg | missense_variant | 0.12 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.12 |
rpoB | 760331 | c.525G>T | synonymous_variant | 0.12 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.13 |
rpoB | 760487 | c.681G>C | synonymous_variant | 0.14 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.23 |
rpoB | 760508 | c.702G>A | synonymous_variant | 0.21 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.17 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.16 |
rpoB | 760541 | c.735G>T | synonymous_variant | 0.16 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.15 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.15 |
rpoB | 760588 | p.Thr261Ile | missense_variant | 0.18 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.18 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.18 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.19 |
rpoB | 760607 | c.801G>C | synonymous_variant | 0.21 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.22 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.22 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.18 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.15 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.15 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.17 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.2 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.24 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.22 |
rpoB | 760869 | p.Val355Leu | missense_variant | 0.22 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 0.22 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.22 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.22 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.22 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.29 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.29 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.29 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.28 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.28 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.32 |
rpoB | 760973 | c.1167G>T | synonymous_variant | 0.31 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.24 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.25 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.24 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.24 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.25 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.23 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.25 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.28 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.22 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.22 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.19 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.2 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.21 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.21 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.21 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.23 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.21 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.2 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.15 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.15 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.16 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.14 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.15 |
rpoB | 761159 | c.1353G>T | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.14 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.13 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.16 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.16 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.17 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.17 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.18 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.17 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.17 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.17 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.16 |
rpoB | 761717 | c.1911C>T | synonymous_variant | 0.14 |
rpoB | 761727 | p.Ser641Gly | missense_variant | 0.15 |
rpoB | 761728 | c.1923dupC | frameshift_variant | 0.15 |
rpoB | 761732 | c.1926C>T | synonymous_variant | 0.15 |
rpoB | 761741 | c.1935G>A | synonymous_variant | 0.15 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.15 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 0.13 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 0.12 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.17 |
rpoB | 761954 | c.2148C>T | synonymous_variant | 0.17 |
rpoB | 761955 | p.Ile717Val | missense_variant | 0.18 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.22 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.26 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.26 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.25 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.22 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.22 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.23 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.22 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.23 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.2 |
rpoB | 762086 | c.2280G>T | synonymous_variant | 0.18 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.18 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.11 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.13 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.12 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.15 |
rpoB | 762221 | c.2415G>A | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.14 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.16 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.16 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.16 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.16 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.15 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.14 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.18 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.21 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.18 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.19 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.18 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.16 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.16 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.15 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.12 |
rpoC | 763450 | c.81G>A | synonymous_variant | 0.17 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.19 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.19 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.22 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.2 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.23 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.27 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.23 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.18 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.18 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.14 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.14 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.17 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.14 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>A | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.15 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.15 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.15 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.15 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.15 |
rpoC | 763768 | c.399C>T | synonymous_variant | 0.15 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.15 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.14 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.14 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.13 |
rpoC | 763801 | c.432C>T | synonymous_variant | 0.13 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.13 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.13 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.22 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.23 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.32 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.32 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.32 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.32 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 0.31 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.31 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.32 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.35 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.39 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.43 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.4 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.4 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.4 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.37 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.38 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.37 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.38 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.37 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.39 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.36 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.36 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.33 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.32 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.31 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.22 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.22 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.23 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.16 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.14 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.16 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.16 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.14 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.14 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.12 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.13 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.12 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.16 |
rpoC | 765868 | c.2499G>A | synonymous_variant | 0.16 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.16 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.19 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.19 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 0.25 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.29 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.31 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.3 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.29 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.3 |
rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 0.31 |
rpoC | 765973 | c.2604C>T | synonymous_variant | 0.26 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.27 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.27 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.22 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.19 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 0.17 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.17 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.14 |
rpoC | 766594 | c.3225G>T | synonymous_variant | 0.13 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.15 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.16 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.22 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.17 |
rpoC | 767100 | p.Lys1244Arg | missense_variant | 0.17 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.17 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.17 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.24 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.24 |
rpoC | 767128 | c.3759C>T | synonymous_variant | 0.24 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.22 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.24 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.24 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.28 |
rpoC | 767180 | p.Ala1271Ser | missense_variant | 0.29 |
rpoC | 767188 | c.3819G>A | synonymous_variant | 0.27 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.25 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.24 |
rpoC | 767203 | c.3834C>G | synonymous_variant | 0.26 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.22 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.23 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.22 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.24 |
rpoC | 767230 | c.3861G>T | synonymous_variant | 0.22 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.22 |
rpoC | 767254 | c.3885G>C | synonymous_variant | 0.25 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.18 |
rpoC | 767264 | p.Ala1299Ser | missense_variant | 0.16 |
rpoC | 767267 | p.Ala1300Asn | missense_variant | 0.17 |
rpoC | 767281 | c.3912C>G | synonymous_variant | 0.17 |
rpoC | 767284 | c.3915C>G | synonymous_variant | 0.17 |
rpoC | 767302 | c.3933C>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.97 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.13 |
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 | 0.14 |
fbiC | 1303367 | p.Thr146Ile | missense_variant | 1.0 |
atpE | 1461101 | c.57T>C | synonymous_variant | 0.1 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.17 |
atpE | 1461146 | c.102G>C | synonymous_variant | 0.17 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.18 |
atpE | 1461155 | c.111C>G | synonymous_variant | 0.16 |
atpE | 1461161 | c.117C>G | synonymous_variant | 0.15 |
atpE | 1461167 | c.123G>T | synonymous_variant | 0.16 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.15 |
atpE | 1461179 | c.135G>T | synonymous_variant | 0.14 |
atpE | 1461182 | c.138A>G | synonymous_variant | 0.13 |
atpE | 1461183 | p.Gly47Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472050 | n.205G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473699 | n.43delG | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474061 | n.404T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474100 | n.443C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474103 | n.446A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474106 | n.449_450insCT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474109 | n.453_454delAT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474376 | n.719T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474413 | n.756A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474415 | n.759_781delCACACGCGCATACGCGCGTGTGA | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474630 | n.973T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475220 | n.1563G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476295 | n.2638C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.19 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.13 |
rpsA | 1833616 | c.75A>T | synonymous_variant | 0.13 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.12 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.13 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.14 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.13 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.12 |
rpsA | 1833697 | c.156C>T | synonymous_variant | 0.12 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.14 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.14 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.12 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.13 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.16 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.16 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.15 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.15 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.17 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.18 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.18 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.19 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.17 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.17 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.25 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.25 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.23 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.24 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.19 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.2 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.15 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.15 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.16 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.15 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.15 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.15 |
rpsA | 1834097 | p.Ser186Thr | missense_variant | 0.12 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.13 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.16 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.2 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.2 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.21 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.19 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.24 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.25 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.27 |
rpsA | 1834405 | c.864C>T | synonymous_variant | 0.26 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.26 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.26 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.3 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.3 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.35 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.32 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.31 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.28 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.25 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.24 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.22 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.26 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.27 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.28 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.31 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.3 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.3 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.3 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.28 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.29 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.29 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.31 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.31 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.32 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.33 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.17 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.17 |
rpsA | 1834684 | c.1143C>G | synonymous_variant | 0.17 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.15 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.13 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.15 |
rpsA | 1834726 | c.1185C>T | synonymous_variant | 0.15 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715349 | c.-17T>C | upstream_gene_variant | 1.0 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
thyA | 3073950 | c.522G>T | synonymous_variant | 0.17 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.17 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.17 |
thyA | 3073971 | c.501C>T | synonymous_variant | 0.19 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073980 | c.492C>T | synonymous_variant | 0.15 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.15 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.12 |
thyA | 3074022 | c.450C>T | synonymous_variant | 0.14 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.15 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.15 |
thyA | 3074045 | c.427C>T | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 0.97 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.18 |
rpoA | 3877596 | c.912G>C | synonymous_variant | 0.17 |
rpoA | 3877602 | c.906C>T | synonymous_variant | 0.17 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.19 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.19 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.19 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.19 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.19 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.19 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.2 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.2 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.19 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.14 |
rpoA | 3877977 | p.Lys177Asn | missense_variant | 0.13 |
rpoA | 3877983 | c.525C>G | synonymous_variant | 0.15 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.15 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.17 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.16 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.14 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.16 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.16 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.16 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.17 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.23 |
rpoA | 3878079 | c.429C>T | synonymous_variant | 0.23 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.22 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.22 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.25 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.25 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.27 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.25 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.26 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.3 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.33 |
rpoA | 3878175 | c.333G>T | synonymous_variant | 0.33 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.31 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.24 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.24 |
rpoA | 3878205 | c.303T>A | synonymous_variant | 0.28 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.27 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.24 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.22 |
rpoA | 3878274 | c.234G>C | synonymous_variant | 0.22 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.24 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.32 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.28 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.27 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.24 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.25 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.24 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.19 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.19 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.18 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.2 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.15 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.16 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.15 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.16 |
rpoA | 3878391 | c.117T>G | synonymous_variant | 0.16 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.14 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.2 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.2 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.14 |
clpC1 | 4038770 | c.1935C>A | synonymous_variant | 0.15 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.15 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.14 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.14 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.14 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.13 |
clpC1 | 4038818 | c.1887G>A | synonymous_variant | 0.13 |
clpC1 | 4038847 | p.Ser620Thr | missense_variant | 0.12 |
clpC1 | 4038860 | c.1845G>T | synonymous_variant | 0.15 |
clpC1 | 4039238 | c.1467C>T | synonymous_variant | 0.18 |
clpC1 | 4039265 | c.1440C>T | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.14 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 0.14 |
clpC1 | 4039280 | c.1425G>T | synonymous_variant | 0.14 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.16 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.18 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.23 |
clpC1 | 4039316 | p.Glu463Asp | missense_variant | 0.21 |
clpC1 | 4039319 | c.1386T>A | synonymous_variant | 0.21 |
clpC1 | 4039322 | c.1383T>G | synonymous_variant | 0.2 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.18 |
clpC1 | 4039336 | c.1369C>T | synonymous_variant | 0.18 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.17 |
clpC1 | 4039346 | p.Arg453Ser | missense_variant | 0.17 |
clpC1 | 4039360 | p.Ser449Arg | missense_variant | 0.22 |
clpC1 | 4039361 | c.1344C>G | synonymous_variant | 0.22 |
clpC1 | 4039391 | c.1314T>C | synonymous_variant | 0.32 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.34 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.37 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.37 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.37 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.36 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.27 |
clpC1 | 4039451 | c.1254G>A | synonymous_variant | 0.3 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.3 |
clpC1 | 4039457 | c.1248C>T | synonymous_variant | 0.3 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.29 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.29 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.28 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.28 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.31 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.31 |
clpC1 | 4039484 | c.1221T>A | synonymous_variant | 0.28 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.24 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.24 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.22 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.18 |
clpC1 | 4039649 | c.1056G>T | synonymous_variant | 0.13 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.15 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.2 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.18 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.21 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.2 |
clpC1 | 4039745 | c.960C>T | synonymous_variant | 0.2 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.18 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.19 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.22 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.21 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.21 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.17 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.18 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.15 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.15 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.16 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.22 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.24 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.28 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.29 |
clpC1 | 4039874 | c.831C>T | synonymous_variant | 0.25 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.33 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.32 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.28 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.28 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.25 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.25 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.24 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.24 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.25 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.26 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.24 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.22 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.21 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.19 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.18 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.16 |
clpC1 | 4040051 | c.654C>T | synonymous_variant | 0.16 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.18 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040126 | c.579C>T | synonymous_variant | 0.13 |
clpC1 | 4040510 | c.195G>A | synonymous_variant | 0.13 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
clpC1 | 4040531 | c.174T>G | synonymous_variant | 0.15 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.15 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.15 |
clpC1 | 4040543 | c.162C>T | synonymous_variant | 0.16 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 0.16 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.16 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.16 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.16 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.15 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.15 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.15 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.14 |
clpC1 | 4040591 | c.114C>T | synonymous_variant | 0.15 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.15 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.15 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.15 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.16 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338498 | p.Glu8Asp | missense_variant | 0.98 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |