Run ID: ERR2446382
Sample name:
Date: 15-08-2022 11:02:24
Number of reads: 2535245
Percentage reads mapped: 99.7
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.39 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5650 | c.411C>A | synonymous_variant | 0.2 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.14 |
gyrB | 6121 | c.882C>T | synonymous_variant | 0.14 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.14 |
gyrB | 6133 | c.894G>C | synonymous_variant | 0.15 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.14 |
gyrB | 6151 | c.912C>T | synonymous_variant | 0.14 |
gyrB | 6184 | c.945C>T | synonymous_variant | 0.14 |
gyrB | 6196 | c.957C>T | synonymous_variant | 0.12 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.16 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.16 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.23 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.26 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.26 |
gyrA | 6640 | c.-662A>C | upstream_gene_variant | 0.26 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.26 |
gyrA | 6646 | c.-656C>T | upstream_gene_variant | 0.32 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.33 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.4 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.4 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.36 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.37 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.4 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.4 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.4 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.36 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.33 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.3 |
gyrA | 6754 | c.-548C>T | upstream_gene_variant | 0.33 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.39 |
gyrA | 6772 | c.-530C>G | upstream_gene_variant | 0.41 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.43 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.48 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.42 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.38 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.41 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.38 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.4 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.39 |
gyrA | 6872 | c.-430_-428delTTGinsCTT | upstream_gene_variant | 0.39 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.41 |
gyrA | 6889 | c.-413G>A | upstream_gene_variant | 0.36 |
gyrA | 6898 | c.-404G>T | upstream_gene_variant | 0.18 |
gyrA | 7355 | c.54T>A | synonymous_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.17 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.17 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.17 |
gyrA | 7403 | c.102C>T | synonymous_variant | 0.2 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.2 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.18 |
gyrA | 7424 | c.123G>C | synonymous_variant | 0.17 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.17 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.15 |
gyrA | 7439 | c.138C>T | synonymous_variant | 0.17 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.17 |
gyrA | 7451 | c.150C>A | synonymous_variant | 0.17 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.17 |
gyrA | 7511 | c.210C>T | synonymous_variant | 0.19 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.19 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.19 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.24 |
gyrA | 7553 | c.252C>T | synonymous_variant | 0.25 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.29 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.29 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.38 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.35 |
gyrA | 7595 | c.294C>T | synonymous_variant | 0.4 |
gyrA | 7607 | c.306C>T | synonymous_variant | 0.4 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.12 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.12 |
gyrA | 8633 | c.1332C>G | synonymous_variant | 0.12 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.12 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.12 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.12 |
gyrA | 8649 | p.Arg450Lys | missense_variant | 0.14 |
gyrA | 8666 | c.1365G>C | synonymous_variant | 0.14 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.14 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.13 |
gyrA | 8696 | c.1395G>C | synonymous_variant | 0.13 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.13 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.15 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.17 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.2 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.19 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.21 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.24 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.28 |
gyrA | 8921 | c.1620C>T | synonymous_variant | 0.32 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.32 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.31 |
gyrA | 8946 | c.1645T>C | synonymous_variant | 0.31 |
gyrA | 8957 | c.1656C>T | synonymous_variant | 0.32 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.3 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 0.28 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.25 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.26 |
gyrA | 8993 | c.1692C>T | synonymous_variant | 0.26 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.25 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.25 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.24 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.18 |
gyrA | 9171 | p.Val624Leu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.15 |
fgd1 | 491112 | c.330G>C | synonymous_variant | 0.3 |
fgd1 | 491115 | c.333G>C | synonymous_variant | 0.3 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.3 |
fgd1 | 491137 | p.Glu119Ile | missense_variant | 0.36 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.38 |
fgd1 | 491166 | c.384G>T | synonymous_variant | 0.38 |
fgd1 | 491172 | c.390C>G | synonymous_variant | 0.36 |
fgd1 | 491184 | c.402A>G | synonymous_variant | 0.42 |
fgd1 | 491190 | c.408G>C | synonymous_variant | 0.42 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.42 |
fgd1 | 491196 | c.414A>C | synonymous_variant | 0.42 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.45 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.45 |
fgd1 | 491213 | p.Ser144Thr | missense_variant | 0.4 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.13 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.13 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.14 |
mshA | 575740 | c.393G>T | synonymous_variant | 0.14 |
mshA | 575761 | c.414C>G | synonymous_variant | 0.12 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.12 |
mshA | 575797 | p.Ile150Met | missense_variant | 0.12 |
rpoB | 759623 | c.-184C>A | upstream_gene_variant | 0.17 |
rpoB | 759772 | c.-35C>A | upstream_gene_variant | 0.2 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.18 |
rpoB | 760110 | c.304_306delTCTinsAGC | synonymous_variant | 0.2 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.27 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.23 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.25 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.35 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.5 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.5 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.5 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.52 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.48 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.45 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.33 |
rpoB | 760276 | p.Lys157Met | missense_variant | 0.33 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.31 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.15 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.23 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.23 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.27 |
rpoB | 760388 | c.582C>T | synonymous_variant | 0.36 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.43 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.44 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.44 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.47 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.5 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.47 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.56 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.5 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.5 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.47 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.47 |
rpoB | 760588 | p.Thr261Ile | missense_variant | 0.64 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.7 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.7 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.64 |
rpoB | 760608 | c.802C>T | synonymous_variant | 0.64 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.62 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.58 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.54 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.5 |
rpoB | 760661 | c.855A>G | synonymous_variant | 0.5 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.5 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.55 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.55 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.6 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.4 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.4 |
rpoB | 760886 | p.Glu360Asp | missense_variant | 0.36 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.36 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.33 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.33 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.18 |
rpoB | 760943 | c.1137C>T | synonymous_variant | 0.19 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.19 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.18 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.18 |
rpoB | 760973 | c.1167G>T | synonymous_variant | 0.2 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.14 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.15 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.15 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.21 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.27 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.35 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.37 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.4 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.43 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.45 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.55 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.55 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.55 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.52 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.52 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.58 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.52 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.52 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.44 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.44 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.38 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.33 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.13 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.25 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.23 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.18 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.18 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.18 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.25 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.24 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.25 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.25 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.22 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.22 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.22 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.22 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.24 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 0.44 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.43 |
rpoB | 761333 | c.1527G>T | synonymous_variant | 0.36 |
rpoB | 761339 | c.1533C>G | synonymous_variant | 0.42 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.36 |
rpoB | 761346 | p.Val514Ser | missense_variant | 0.33 |
rpoB | 761354 | c.1548C>A | synonymous_variant | 0.33 |
rpoB | 761357 | c.1551G>T | synonymous_variant | 0.31 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.31 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.33 |
rpoB | 761369 | p.Glu521Asp | missense_variant | 0.33 |
rpoB | 761373 | p.Val523His | missense_variant | 0.31 |
rpoB | 761384 | c.1578C>G | synonymous_variant | 0.29 |
rpoB | 761393 | c.1587G>A | synonymous_variant | 0.31 |
rpoB | 761528 | c.1722C>T | synonymous_variant | 0.26 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.29 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.35 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.35 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.36 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.36 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.35 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.35 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.4 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.4 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.35 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.31 |
rpoB | 761657 | c.1851C>T | synonymous_variant | 0.21 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.21 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.23 |
rpoB | 761936 | c.2130C>T | synonymous_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.15 |
rpoB | 761954 | c.2148C>A | synonymous_variant | 0.19 |
rpoB | 761955 | p.Ile717Val | missense_variant | 0.19 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.29 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.34 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.38 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.39 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.45 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.43 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.38 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.4 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.35 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.24 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.24 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.19 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.24 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.27 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.17 |
rpoB | 762134 | c.2328C>A | synonymous_variant | 0.17 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.17 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 0.17 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.17 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.17 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.28 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.22 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.22 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.22 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.24 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.27 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.27 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.22 |
rpoB | 762323 | c.2517C>A | synonymous_variant | 0.21 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.18 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.19 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.32 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.32 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.44 |
rpoB | 762450 | p.Arg882Ser | missense_variant | 0.56 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.46 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.5 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.5 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.42 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.46 |
rpoC | 762515 | c.-855C>T | upstream_gene_variant | 0.4 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.18 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.18 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.18 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.18 |
rpoC | 762866 | c.-504C>T | upstream_gene_variant | 0.23 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.5 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.56 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.59 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.53 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.52 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.52 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.58 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.64 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.64 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.65 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.7 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.64 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.67 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.54 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.52 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.54 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.61 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.5 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.46 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.48 |
rpoC | 763145 | c.-225G>A | upstream_gene_variant | 0.46 |
rpoC | 763157 | c.-213G>T | upstream_gene_variant | 0.44 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.5 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 0.47 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.36 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.21 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.17 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.39 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.42 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.45 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.5 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.45 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.35 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.28 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.29 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.24 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.25 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.28 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.24 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.24 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.27 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.26 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.26 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.25 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.27 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.27 |
rpoC | 763732 | c.363C>A | synonymous_variant | 0.3 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.32 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.3 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.3 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.29 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.22 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.19 |
rpoC | 763782 | c.415delG | frameshift_variant | 0.13 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.21 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.26 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 0.28 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.28 |
rpoC | 763947 | p.Ala193Val | missense_variant | 0.29 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.29 |
rpoC | 763960 | c.591T>G | synonymous_variant | 0.38 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.35 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.31 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.28 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.28 |
rpoC | 763999 | c.630C>T | synonymous_variant | 0.28 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.29 |
rpoC | 764003 | p.Ala212Ser | missense_variant | 0.31 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.31 |
rpoC | 764029 | p.Glu220Asp | missense_variant | 0.23 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.21 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.23 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.23 |
rpoC | 764054 | c.685C>T | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.15 |
rpoC | 764332 | c.963G>A | synonymous_variant | 0.2 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.24 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.24 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.24 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.24 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.24 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.25 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.27 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.28 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.33 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.33 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.33 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.32 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.27 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.27 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.42 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.38 |
rpoC | 764524 | c.1155C>G | synonymous_variant | 0.42 |
rpoC | 764530 | c.1161C>G | synonymous_variant | 0.44 |
rpoC | 764534 | c.1165C>A | synonymous_variant | 0.44 |
rpoC | 764539 | c.1170C>T | synonymous_variant | 0.42 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.48 |
rpoC | 764545 | c.1176C>A | synonymous_variant | 0.44 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.46 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.48 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.42 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.35 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.33 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.3 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.38 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.36 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.29 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.3 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.25 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.26 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.3 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.28 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.19 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.19 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.18 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.19 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.18 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.18 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.22 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.23 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.25 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.24 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.17 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.17 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.19 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.19 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.15 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.26 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.22 |
rpoC | 765004 | c.1635G>C | synonymous_variant | 0.21 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.21 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.21 |
rpoC | 765011 | c.1642_1644delAGCinsTCG | synonymous_variant | 0.2 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.22 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.29 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.32 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.29 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.28 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.26 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.18 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.14 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.14 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.14 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.15 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.14 |
rpoC | 765100 | c.1731G>C | synonymous_variant | 0.14 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.15 |
rpoC | 765370 | c.2001G>C | synonymous_variant | 0.2 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.2 |
rpoC | 765382 | c.2013G>T | synonymous_variant | 0.2 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.24 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.3 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.29 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.3 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.42 |
rpoC | 765449 | p.Ala694Ser | missense_variant | 0.35 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.38 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.35 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.32 |
rpoC | 765480 | p.Tyr704Phe | missense_variant | 0.32 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.26 |
rpoC | 765517 | c.2148C>G | synonymous_variant | 0.21 |
rpoC | 765533 | p.Tyr722His | missense_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.12 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.2 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.25 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 0.24 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.25 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.26 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.31 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.21 |
rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 0.14 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.15 |
rpoC | 765973 | c.2604C>G | synonymous_variant | 0.12 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.12 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.12 |
rpoC | 766333 | c.2964G>T | synonymous_variant | 0.18 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.16 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.15 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.15 |
rpoC | 766353 | p.Val995Ala | missense_variant | 0.15 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.16 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 0.16 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.16 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.17 |
rpoC | 766393 | c.3024C>T | synonymous_variant | 0.17 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.16 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.14 |
rpoC | 766507 | c.3138C>T | synonymous_variant | 0.15 |
rpoC | 766513 | c.3144C>T | synonymous_variant | 0.16 |
rpoC | 766522 | c.3153C>A | synonymous_variant | 0.15 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.15 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.17 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 0.16 |
rpoC | 766537 | c.3168G>A | synonymous_variant | 0.15 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.15 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.15 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.15 |
rpoC | 766573 | c.3204T>G | synonymous_variant | 0.15 |
rpoC | 766594 | c.3225G>T | synonymous_variant | 0.15 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.17 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.18 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.14 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.21 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.31 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.41 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.38 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.39 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.36 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.32 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.26 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.23 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.29 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.31 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.3 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.32 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.32 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.3 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.31 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.3 |
rpoC | 767179 | c.3810C>T | synonymous_variant | 0.23 |
rpoC | 767180 | p.Ala1271Ser | missense_variant | 0.23 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.29 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.29 |
rpoC | 767203 | c.3834C>G | synonymous_variant | 0.27 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.27 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.27 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.26 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.25 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.19 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.17 |
rpoC | 767254 | c.3885G>C | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776302 | p.Met727Val | missense_variant | 0.12 |
mmpS5 | 778898 | p.Gly3Val | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781559 | c.-1G>C | upstream_gene_variant | 0.3 |
rpsL | 781572 | p.Gln5Asn | missense_variant | 0.43 |
rpsL | 781586 | c.27C>T | synonymous_variant | 0.5 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.57 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.57 |
rpsL | 781616 | c.57C>G | synonymous_variant | 0.73 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.73 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.6 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.6 |
rpsL | 781658 | c.99A>C | synonymous_variant | 0.53 |
rpsL | 781670 | c.111G>C | synonymous_variant | 0.43 |
rpsL | 781706 | c.147T>C | synonymous_variant | 0.14 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.17 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.17 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.17 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.46 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.57 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.57 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.53 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.57 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.57 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.47 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.47 |
rpsL | 781877 | c.318T>A | synonymous_variant | 0.5 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.4 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.4 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.4 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.27 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.17 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.17 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.12 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.12 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.2 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.42 |
atpE | 1461146 | c.102G>T | synonymous_variant | 0.46 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.46 |
atpE | 1461161 | c.117C>G | synonymous_variant | 0.46 |
atpE | 1461164 | c.120C>T | synonymous_variant | 0.43 |
atpE | 1461167 | c.123G>T | synonymous_variant | 0.43 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.4 |
atpE | 1461179 | c.135G>T | synonymous_variant | 0.4 |
atpE | 1461182 | c.138A>G | synonymous_variant | 0.38 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.38 |
atpE | 1461197 | c.153A>C | synonymous_variant | 0.38 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.46 |
atpE | 1461230 | c.186G>T | synonymous_variant | 0.36 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.36 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.42 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472050 | n.205G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473684 | n.27G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473699 | n.43delG | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.31 |
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 | 0.43 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473770 | n.113T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475954 | n.2297A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475959 | n.2302C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476454 | n.2797C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
inhA | 1674876 | c.675C>T | synonymous_variant | 0.25 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.31 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.33 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.33 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.33 |
inhA | 1674909 | c.708G>A | synonymous_variant | 0.33 |
inhA | 1674912 | c.711G>C | synonymous_variant | 0.36 |
inhA | 1674915 | c.714C>G | synonymous_variant | 0.36 |
inhA | 1674942 | c.741T>C | synonymous_variant | 0.4 |
inhA | 1674949 | c.748C>T | synonymous_variant | 0.4 |
inhA | 1674966 | c.765T>C | synonymous_variant | 0.4 |
rpsA | 1833517 | c.-24delC | upstream_gene_variant | 0.12 |
rpsA | 1833536 | c.-6A>C | upstream_gene_variant | 0.17 |
rpsA | 1833547 | c.6G>A | synonymous_variant | 0.18 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.23 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.24 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.24 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.3 |
rpsA | 1833616 | c.75A>T | synonymous_variant | 0.33 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.29 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.39 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.35 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.3 |
rpsA | 1833679 | c.138G>T | synonymous_variant | 0.28 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.29 |
rpsA | 1833691 | c.150G>A | synonymous_variant | 0.25 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.25 |
rpsA | 1833697 | c.156C>T | synonymous_variant | 0.25 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.26 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.24 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.21 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.22 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.2 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.2 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.15 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.16 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.15 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.22 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.25 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.25 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.25 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.24 |
rpsA | 1833823 | c.282G>A | synonymous_variant | 0.4 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.44 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.44 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.42 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.4 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.47 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.52 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.5 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.48 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.45 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.56 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.5 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.52 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.5 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.52 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.5 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.46 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.43 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.45 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.45 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.43 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.38 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.36 |
rpsA | 1834073 | p.Lys178Arg | missense_variant | 0.17 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.1 |
rpsA | 1834228 | c.687C>A | synonymous_variant | 0.25 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.24 |
rpsA | 1834234 | c.693G>T | synonymous_variant | 0.24 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.24 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.25 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.23 |
rpsA | 1834252 | c.711C>G | synonymous_variant | 0.25 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.24 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.23 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.3 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.24 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.28 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.22 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.22 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.37 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.42 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.44 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.48 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.45 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.47 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 0.47 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.47 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.52 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 0.55 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 0.53 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.53 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.52 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.42 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.44 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.41 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.5 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.45 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.45 |
rpsA | 1834534 | c.993C>T | synonymous_variant | 0.5 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.5 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.4 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.4 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.5 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.47 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.5 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.5 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.56 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.53 |
rpsA | 1834645 | c.1104C>T | synonymous_variant | 0.58 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.57 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.57 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.5 |
rpsA | 1834698 | c.1157_1158insC | frameshift_variant | 0.48 |
rpsA | 1834701 | p.Gln387Pro | missense_variant | 0.48 |
rpsA | 1834704 | c.1164delC | frameshift_variant | 0.48 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.42 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.42 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.44 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.42 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.35 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.35 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.15 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 0.15 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.13 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.23 |
rpsA | 1834813 | c.1272G>T | synonymous_variant | 0.17 |
rpsA | 1834830 | p.Ala430Val | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154915 | c.1197A>G | synonymous_variant | 1.0 |
PPE35 | 2168186 | c.2427C>T | synonymous_variant | 0.13 |
PPE35 | 2169383 | c.1230C>G | synonymous_variant | 0.81 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289919 | c.-678C>T | upstream_gene_variant | 0.17 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.33 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.29 |
kasA | 2517953 | c.-162C>T | upstream_gene_variant | 0.21 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.16 |
kasA | 2518726 | c.612G>C | synonymous_variant | 0.2 |
kasA | 2518738 | c.624G>C | synonymous_variant | 0.27 |
kasA | 2518756 | c.642G>C | synonymous_variant | 0.36 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.36 |
kasA | 2518771 | c.657C>G | synonymous_variant | 0.33 |
kasA | 2518774 | c.660C>T | synonymous_variant | 0.31 |
kasA | 2518783 | c.669T>G | synonymous_variant | 0.31 |
kasA | 2518787 | p.Arg225Lys | missense_variant | 0.31 |
kasA | 2518792 | c.678C>T | synonymous_variant | 0.25 |
kasA | 2518795 | c.681C>T | synonymous_variant | 0.25 |
kasA | 2518798 | c.684G>C | synonymous_variant | 0.25 |
kasA | 2518822 | c.708C>A | synonymous_variant | 0.2 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087095 | p.Phe92Leu | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877542 | c.966C>A | synonymous_variant | 0.25 |
rpoA | 3877545 | c.963G>T | synonymous_variant | 0.27 |
rpoA | 3877554 | c.954G>A | synonymous_variant | 0.29 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 0.31 |
rpoA | 3877563 | c.945C>T | synonymous_variant | 0.31 |
rpoA | 3877569 | p.Pro313Thr | missense_variant | 0.29 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.4 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.45 |
rpoA | 3877614 | c.894G>A | synonymous_variant | 0.43 |
rpoA | 3877620 | c.888G>A | synonymous_variant | 0.43 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.38 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.33 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.26 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.31 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.31 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.29 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.29 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.32 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.26 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 0.25 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.25 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.25 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 0.28 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.29 |
rpoA | 3877755 | c.753C>T | synonymous_variant | 0.28 |
rpoA | 3877758 | c.750G>C | synonymous_variant | 0.28 |
rpoA | 3877764 | c.744C>A | synonymous_variant | 0.29 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.29 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.29 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.33 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.37 |
rpoA | 3877797 | c.711G>A | synonymous_variant | 0.42 |
rpoA | 3877815 | c.693C>T | synonymous_variant | 0.37 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.39 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.44 |
rpoA | 3877839 | c.669G>A | synonymous_variant | 0.47 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.56 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.61 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.61 |
rpoA | 3877896 | c.612G>A | synonymous_variant | 0.65 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.65 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.65 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.59 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.57 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.55 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.45 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.41 |
rpoA | 3877974 | c.534G>T | synonymous_variant | 0.41 |
rpoA | 3877977 | p.Lys177Asn | missense_variant | 0.35 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.33 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.2 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.27 |
rpoA | 3878142 | p.Gly122Asp | missense_variant | 0.43 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.48 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.5 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.5 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.52 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.52 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.52 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.56 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.59 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.7 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.69 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.62 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.54 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.47 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.43 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.5 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.53 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.6 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.6 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.52 |
rpoA | 3878343 | c.165C>T | synonymous_variant | 0.5 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.47 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.44 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.44 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.47 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.47 |
rpoA | 3878381 | c.127C>T | synonymous_variant | 0.47 |
rpoA | 3878391 | c.117T>G | synonymous_variant | 0.5 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.47 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.13 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.13 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.14 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.14 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.14 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.14 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.15 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.17 |
clpC1 | 4039528 | c.1177C>A | synonymous_variant | 0.16 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.15 |
clpC1 | 4039544 | c.1161C>T | synonymous_variant | 0.14 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.14 |
clpC1 | 4039565 | c.1140G>T | synonymous_variant | 0.13 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.11 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.12 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.12 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.12 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.11 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
clpC1 | 4040531 | c.174T>G | synonymous_variant | 0.16 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.14 |
clpC1 | 4040558 | c.147G>C | synonymous_variant | 0.12 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.13 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.13 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.13 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.13 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.13 |
embC | 4240381 | p.Gln173His | missense_variant | 0.18 |
embC | 4240729 | c.867C>G | synonymous_variant | 0.2 |
embC | 4240735 | c.873C>G | synonymous_variant | 0.25 |
embC | 4240741 | c.879C>T | synonymous_variant | 0.26 |
embC | 4240756 | c.894G>C | synonymous_variant | 0.32 |
embC | 4240771 | c.909G>C | synonymous_variant | 0.3 |
embC | 4240772 | p.Ser304Ala | missense_variant | 0.3 |
embC | 4240778 | p.His306Gly | missense_variant | 0.32 |
embC | 4240781 | p.Ala307Ser | missense_variant | 0.33 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.44 |
embC | 4240819 | c.957A>C | synonymous_variant | 0.5 |
embC | 4240826 | p.Ala322Ser | missense_variant | 0.52 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.48 |
embC | 4240856 | p.Ala332Thr | missense_variant | 0.42 |
embC | 4240859 | p.Leu333Ile | missense_variant | 0.42 |
embC | 4240876 | c.1014C>T | synonymous_variant | 0.27 |
embC | 4240879 | c.1017G>T | synonymous_variant | 0.27 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.27 |
embC | 4240886 | p.Ile342Val | missense_variant | 0.27 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.25 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245974 | c.-540C>A | upstream_gene_variant | 0.15 |
embA | 4246367 | p.Tyr1045* | stop_gained | 0.14 |
embB | 4247455 | c.942C>G | synonymous_variant | 0.2 |
embB | 4248779 | p.Glu756* | stop_gained | 0.2 |
aftB | 4268617 | p.Gly74Cys | missense_variant | 0.2 |
ethA | 4326360 | p.Met372Leu | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408012 | p.Arg64Leu | missense_variant | 0.18 |
gid | 4408358 | c.-156C>G | upstream_gene_variant | 1.0 |