Run ID: SRR8692800
Sample name:
Date: 13-08-2023 20:44:19
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.24 | streptomycin |
rplC | 801268 | p.Cys154Arg | missense_variant | 0.33 | linezolid |
ethA | 4326426 | c.1047delT | frameshift_variant | 0.15 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5260 | p.Lys7Asn | missense_variant | 0.2 |
gyrB | 5270 | p.Glu11* | stop_gained | 0.2 |
gyrB | 5493 | p.Pro85Gln | missense_variant | 0.14 |
gyrB | 5990 | p.Phe251Leu | missense_variant | 0.14 |
gyrB | 6154 | c.915C>A | synonymous_variant | 0.25 |
gyrB | 6246 | p.Lys336Arg | missense_variant | 0.25 |
gyrA | 6334 | c.-968G>T | upstream_gene_variant | 0.22 |
gyrB | 6426 | p.Phe396Tyr | missense_variant | 0.4 |
gyrB | 6750 | p.Ala504Glu | missense_variant | 0.17 |
gyrB | 6972 | p.Pro578Gln | missense_variant | 0.21 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.33 |
gyrA | 7506 | p.Ser69Gly | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.22 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.18 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.15 |
gyrA | 7632 | p.Asp111His | missense_variant | 0.15 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.15 |
gyrA | 7716 | p.Met139Leu | missense_variant | 0.13 |
gyrA | 7729 | p.Arg143Lys | missense_variant | 0.14 |
gyrA | 8791 | p.Arg497Leu | missense_variant | 0.14 |
gyrA | 8801 | c.1500G>T | synonymous_variant | 0.14 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.14 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.14 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.12 |
gyrA | 9266 | p.Asp655Glu | missense_variant | 0.15 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.15 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.16 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.15 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.16 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.26 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.17 |
gyrA | 9325 | p.Ser675Cys | missense_variant | 0.15 |
gyrA | 9335 | c.2034G>T | synonymous_variant | 0.14 |
gyrA | 9521 | c.2220C>T | synonymous_variant | 0.17 |
fgd1 | 491157 | c.375C>T | synonymous_variant | 0.17 |
fgd1 | 491613 | c.831C>A | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.33 |
mshA | 575248 | c.-99delG | upstream_gene_variant | 0.12 |
mshA | 575265 | c.-83C>A | upstream_gene_variant | 0.14 |
mshA | 575279 | c.-69C>A | upstream_gene_variant | 0.17 |
mshA | 575282 | c.-66C>T | upstream_gene_variant | 0.17 |
mshA | 575373 | p.Gly9Val | missense_variant | 0.29 |
mshA | 575682 | p.Val112Ala | missense_variant | 0.2 |
mshA | 575717 | p.Asp124Tyr | missense_variant | 0.15 |
mshA | 576318 | p.Arg324Leu | missense_variant | 0.4 |
ccsA | 620456 | p.Ala189Asp | missense_variant | 0.17 |
ccsA | 620529 | c.639G>T | synonymous_variant | 0.18 |
ccsA | 620592 | c.702C>A | synonymous_variant | 0.2 |
ccsA | 620674 | p.Asp262Tyr | missense_variant | 0.22 |
rpoB | 759809 | c.3G>T | start_lost | 0.2 |
rpoB | 760176 | p.Ala124Ser | missense_variant | 0.15 |
rpoB | 760211 | c.405C>T | synonymous_variant | 0.17 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.25 |
rpoB | 760405 | p.Pro200Gln | missense_variant | 0.2 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.22 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.22 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.22 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.29 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.15 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.17 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.18 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.18 |
rpoB | 761049 | p.Arg415Ser | missense_variant | 0.22 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.22 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.22 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.22 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.22 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.33 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.22 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.18 |
rpoB | 761445 | p.Arg547Ser | missense_variant | 0.15 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.18 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.23 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.23 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.23 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.21 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.17 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.16 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.16 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.18 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.12 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.12 |
rpoB | 761849 | c.2043C>T | synonymous_variant | 0.18 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.18 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.15 |
rpoB | 761984 | p.Glu726Asp | missense_variant | 0.18 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.15 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.17 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.17 |
rpoB | 762028 | p.Leu741Pro | missense_variant | 0.18 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.15 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.17 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.18 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.12 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.16 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.17 |
rpoC | 762449 | c.-921C>G | upstream_gene_variant | 0.16 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.16 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.22 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.22 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.22 |
rpoB | 762507 | p.Leu901Met | missense_variant | 0.22 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.22 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.2 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.2 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.2 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.33 |
rpoC | 762560 | c.-810A>T | upstream_gene_variant | 0.3 |
rpoC | 762563 | c.-807G>T | upstream_gene_variant | 0.3 |
rpoB | 762685 | p.Ala960Glu | missense_variant | 0.22 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.16 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.15 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.16 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.15 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.12 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.16 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.19 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.19 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.23 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.17 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.17 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.2 |
rpoC | 763079 | c.-291C>G | upstream_gene_variant | 0.2 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.19 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.19 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.19 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.12 |
rpoC | 763375 | c.6C>A | synonymous_variant | 0.25 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.31 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.31 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.31 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.33 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.33 |
rpoC | 763443 | p.Tyr25Phe | missense_variant | 0.33 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.31 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.31 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.55 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.46 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.17 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.17 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.2 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.2 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.16 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.21 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.19 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.15 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.15 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.15 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.14 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.14 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.15 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.19 |
rpoC | 763861 | c.492C>T | synonymous_variant | 0.19 |
rpoC | 763867 | c.498C>T | synonymous_variant | 0.19 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.19 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.19 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.2 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.23 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.25 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.25 |
rpoC | 763903 | c.534G>A | synonymous_variant | 0.27 |
rpoC | 763925 | p.Ala186Lys | missense_variant | 0.18 |
rpoC | 763930 | c.561G>A | synonymous_variant | 0.18 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 0.15 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.18 |
rpoC | 763947 | p.Ala193Val | missense_variant | 0.18 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.18 |
rpoC | 763960 | c.591T>G | synonymous_variant | 0.2 |
rpoC | 763963 | c.594C>T | synonymous_variant | 0.2 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.17 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.17 |
rpoC | 764472 | p.Asn368Ser | missense_variant | 0.18 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.22 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.18 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.18 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.25 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.38 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.4 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.4 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.3 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.27 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.2 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.27 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.25 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.36 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.36 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.33 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.36 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.36 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.29 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.29 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.22 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.21 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.22 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.17 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.17 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.15 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.15 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.14 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.15 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.15 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.15 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.15 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.15 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.15 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.14 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.15 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.17 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.15 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.18 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.18 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.19 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.18 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.18 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.18 |
mmpL5 | 775794 | p.Ala896Val | missense_variant | 0.25 |
mmpL5 | 775835 | c.2646C>A | synonymous_variant | 0.15 |
mmpL5 | 775865 | c.2616T>C | synonymous_variant | 0.17 |
mmpL5 | 775885 | p.Ile866Leu | missense_variant | 0.18 |
mmpL5 | 775886 | c.2595A>T | synonymous_variant | 0.18 |
mmpL5 | 775889 | c.2592C>G | synonymous_variant | 0.18 |
mmpL5 | 775905 | p.Lys859Arg | missense_variant | 0.14 |
mmpL5 | 775909 | p.Leu858Ile | missense_variant | 0.14 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.2 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.12 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.2 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.16 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.13 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.2 |
mmpL5 | 777584 | p.Tyr299* | stop_gained | 0.25 |
mmpL5 | 777692 | c.789C>T | synonymous_variant | 0.17 |
mmpL5 | 777695 | c.786G>T | synonymous_variant | 0.17 |
mmpL5 | 778606 | c.-126C>T | upstream_gene_variant | 0.17 |
mmpR5 | 779096 | p.Ala36Glu | missense_variant | 0.2 |
mmpR5 | 779294 | p.Ala102Asp | missense_variant | 0.17 |
mmpR5 | 779374 | p.Pro129Thr | missense_variant | 0.29 |
rpsL | 781553 | c.-7C>T | upstream_gene_variant | 0.15 |
rpsL | 781580 | c.21G>T | synonymous_variant | 0.17 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.15 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.15 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.14 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.14 |
rpsL | 781616 | c.57C>G | synonymous_variant | 0.15 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.14 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.15 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.12 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.12 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.12 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.43 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.44 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.42 |
rplC | 800639 | c.-170C>T | upstream_gene_variant | 0.42 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.38 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.36 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.33 |
rplC | 800678 | c.-131C>T | upstream_gene_variant | 0.2 |
rplC | 800684 | c.-125G>A | upstream_gene_variant | 0.14 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.14 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.13 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.13 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.13 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.13 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.12 |
rplC | 800855 | p.Val16Ala | missense_variant | 0.17 |
rplC | 801070 | p.Asp88Tyr | missense_variant | 0.22 |
rplC | 801381 | c.573G>T | synonymous_variant | 0.25 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 1.0 |
Rv1258c | 1406761 | p.Glu194* | stop_gained | 0.25 |
embR | 1416727 | c.621G>T | synonymous_variant | 0.18 |
embR | 1416785 | p.Ser188Ile | missense_variant | 0.13 |
embR | 1416954 | p.Glu132* | stop_gained | 0.18 |
embR | 1417043 | p.Arg102Leu | missense_variant | 0.14 |
atpE | 1460982 | c.-63G>T | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471798 | n.-48G>T | upstream_gene_variant | 0.4 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.43 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472301 | n.456C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473847 | n.190G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474561 | n.904G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475192 | n.1535C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475286 | n.1629T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475296 | n.1639G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475428 | n.1771G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476339 | n.2682G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476419 | n.2762G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476438 | n.2781G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.6 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.18 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.18 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.18 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.2 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.18 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.18 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.16 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.38 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.38 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.33 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.36 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.42 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.38 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.42 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.38 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.45 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.42 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.36 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.36 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.15 |
rpsA | 1834705 | c.1164C>G | synonymous_variant | 0.11 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.17 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.18 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.18 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.15 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.14 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.14 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.15 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.14 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 0.16 |
tlyA | 1917978 | c.39G>A | synonymous_variant | 0.14 |
tlyA | 1918190 | p.Arg84Gln | missense_variant | 0.17 |
tlyA | 1918242 | c.303G>A | synonymous_variant | 0.18 |
tlyA | 1918520 | p.Pro194Leu | missense_variant | 0.14 |
ndh | 2101817 | p.Thr409Asn | missense_variant | 0.2 |
ndh | 2102917 | c.126G>A | synonymous_variant | 0.33 |
ndh | 2103123 | c.-81G>T | upstream_gene_variant | 0.5 |
katG | 2154245 | p.Glu623Lys | missense_variant | 0.18 |
katG | 2154248 | p.Pro622Thr | missense_variant | 0.18 |
katG | 2154455 | p.Glu553* | stop_gained | 0.2 |
katG | 2154806 | p.Leu436Met | missense_variant | 0.14 |
katG | 2156404 | c.-293G>T | upstream_gene_variant | 0.18 |
katG | 2156447 | c.-336C>G | upstream_gene_variant | 0.13 |
katG | 2156539 | c.-428G>T | upstream_gene_variant | 0.14 |
katG | 2156558 | c.-447G>T | upstream_gene_variant | 0.17 |
katG | 2156568 | c.-457G>T | upstream_gene_variant | 0.17 |
PPE35 | 2168354 | c.2259G>A | synonymous_variant | 0.13 |
PPE35 | 2168742 | p.Gly624Val | missense_variant | 0.17 |
PPE35 | 2169133 | p.Ala494Ser | missense_variant | 0.13 |
PPE35 | 2169310 | p.Gly435Cys | missense_variant | 0.18 |
PPE35 | 2169797 | c.816G>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.14 |
pncA | 2289780 | c.-539C>A | upstream_gene_variant | 0.25 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.27 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.27 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.33 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.3 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.22 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.22 |
kasA | 2518014 | c.-101G>T | upstream_gene_variant | 0.25 |
kasA | 2518564 | c.450C>T | synonymous_variant | 0.13 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.14 |
kasA | 2518570 | c.456G>A | synonymous_variant | 0.14 |
kasA | 2518573 | c.459G>C | synonymous_variant | 0.14 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.14 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.15 |
kasA | 2518582 | c.468G>C | synonymous_variant | 0.15 |
kasA | 2518583 | p.Gln157Glu | missense_variant | 0.15 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.15 |
kasA | 2518603 | c.489G>C | synonymous_variant | 0.14 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.15 |
kasA | 2518612 | c.498C>G | synonymous_variant | 0.15 |
kasA | 2518615 | c.501G>C | synonymous_variant | 0.13 |
kasA | 2518618 | c.504G>T | synonymous_variant | 0.13 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.14 |
kasA | 2518644 | p.Ala177Gly | missense_variant | 0.14 |
kasA | 2518657 | c.543G>A | synonymous_variant | 0.15 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.12 |
kasA | 2518715 | p.Pro201Ala | missense_variant | 0.12 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.17 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.15 |
kasA | 2518756 | c.642G>T | synonymous_variant | 0.21 |
kasA | 2518759 | c.645C>G | synonymous_variant | 0.16 |
kasA | 2518780 | p.Glu222Asp | missense_variant | 0.16 |
kasA | 2518783 | c.669T>G | synonymous_variant | 0.18 |
kasA | 2518787 | p.Arg225Gly | missense_variant | 0.18 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.19 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.18 |
kasA | 2518798 | c.684G>T | synonymous_variant | 0.19 |
kasA | 2518813 | c.699C>T | synonymous_variant | 0.19 |
kasA | 2518816 | c.702C>T | synonymous_variant | 0.21 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.27 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.27 |
kasA | 2518828 | c.714G>C | synonymous_variant | 0.27 |
kasA | 2518849 | c.735G>C | synonymous_variant | 0.2 |
kasA | 2518853 | p.Leu247Ile | missense_variant | 0.2 |
kasA | 2519158 | c.1044C>A | synonymous_variant | 0.18 |
kasA | 2519201 | p.Arg363Ser | missense_variant | 0.22 |
kasA | 2519215 | c.1101C>A | synonymous_variant | 0.18 |
kasA | 2519225 | p.Leu371Met | missense_variant | 0.18 |
eis | 2714171 | p.Ala388Ser | missense_variant | 0.2 |
eis | 2714190 | p.Gln381His | missense_variant | 0.2 |
eis | 2715222 | c.111G>T | synonymous_variant | 0.2 |
eis | 2715320 | p.Leu5Met | missense_variant | 0.18 |
pepQ | 2859798 | c.621G>T | synonymous_variant | 0.17 |
pepQ | 2859978 | p.Cys147* | stop_gained | 0.15 |
ribD | 2986935 | p.Asp33Tyr | missense_variant | 0.15 |
ribD | 2987507 | c.669G>T | synonymous_variant | 0.22 |
ribD | 2987532 | p.Gly232Trp | missense_variant | 0.2 |
Rv2752c | 3065825 | p.Pro123Thr | missense_variant | 0.33 |
thyX | 3068032 | c.-87G>T | upstream_gene_variant | 0.2 |
thyA | 3074650 | c.-179G>T | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.5 |
ald | 3087482 | c.663G>T | synonymous_variant | 0.18 |
ald | 3087912 | p.Glu365Lys | missense_variant | 0.4 |
fbiD | 3339448 | p.Val111Leu | missense_variant | 0.18 |
Rv3083 | 3448878 | c.375C>A | synonymous_variant | 0.22 |
Rv3083 | 3449409 | c.906C>T | synonymous_variant | 0.15 |
Rv3083 | 3449812 | p.Asp437Tyr | missense_variant | 0.25 |
Rv3083 | 3449856 | p.Met451Ile | missense_variant | 0.2 |
Rv3083 | 3449990 | c.1487G>T | stop_lost&splice_region_variant | 0.15 |
fprA | 3474051 | c.45G>A | synonymous_variant | 0.2 |
Rv3236c | 3612693 | c.424C>A | synonymous_variant | 0.4 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.3 |
Rv3236c | 3612859 | c.258G>T | synonymous_variant | 0.22 |
Rv3236c | 3612935 | p.Gly61Val | missense_variant | 0.2 |
fbiA | 3640667 | p.Ser42Ile | missense_variant | 0.13 |
fbiA | 3640689 | p.Asp49Glu | missense_variant | 0.13 |
fbiB | 3640758 | c.-777G>C | upstream_gene_variant | 0.12 |
fbiA | 3640784 | p.Gln81Arg | missense_variant | 0.12 |
fbiA | 3641060 | p.Trp173Leu | missense_variant | 0.17 |
fbiB | 3641990 | p.Met152Ile | missense_variant | 0.17 |
fbiB | 3642014 | p.Gln160His | missense_variant | 0.15 |
fbiB | 3642098 | c.564G>T | synonymous_variant | 0.22 |
fbiB | 3642783 | p.Asp417Asn | missense_variant | 0.15 |
alr | 3840451 | p.Gly324Trp | missense_variant | 0.33 |
alr | 3841201 | p.Ala74Ser | missense_variant | 0.17 |
alr | 3841232 | c.189G>T | synonymous_variant | 0.25 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.12 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.14 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.14 |
rpoA | 3877860 | c.648C>T | synonymous_variant | 0.16 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.17 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.18 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.18 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.17 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.15 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.16 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.19 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.2 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.13 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.12 |
rpoA | 3878373 | c.135G>A | synonymous_variant | 0.2 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.21 |
ddn | 3986645 | c.-199G>A | upstream_gene_variant | 0.25 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.25 |
clpC1 | 4038589 | p.Arg706Ser | missense_variant | 0.14 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.14 |
clpC1 | 4038631 | c.2074C>A | synonymous_variant | 0.14 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.14 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.2 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.2 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.2 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.21 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.21 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.25 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.27 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.36 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.42 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.42 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.42 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.42 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.5 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.5 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.44 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.5 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.5 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.5 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.57 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.57 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.5 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.29 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.25 |
clpC1 | 4038856 | p.Lys617Glu | missense_variant | 0.29 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.29 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.25 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.25 |
clpC1 | 4039001 | p.Asn568Ala | missense_variant | 0.25 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.2 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.21 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.21 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.21 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.21 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.21 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.21 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.2 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.14 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.14 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.12 |
clpC1 | 4039291 | p.Asp472Tyr | missense_variant | 0.2 |
clpC1 | 4039335 | p.Leu457Pro | missense_variant | 0.18 |
clpC1 | 4039718 | c.987C>G | synonymous_variant | 0.12 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.13 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.13 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.13 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.12 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.12 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.12 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.12 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.12 |
clpC1 | 4039787 | p.Ser306Cys | missense_variant | 0.12 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.15 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.15 |
clpC1 | 4039823 | c.882T>A | synonymous_variant | 0.15 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.18 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.18 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.12 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.13 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.15 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.14 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.17 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.15 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.15 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.17 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.18 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.12 |
clpC1 | 4040090 | p.Ser205Cys | missense_variant | 0.12 |
clpC1 | 4040679 | p.Ala9Val | missense_variant | 0.14 |
clpC1 | 4040745 | c.-41G>T | upstream_gene_variant | 0.25 |
panD | 4044258 | c.24G>A | synonymous_variant | 0.25 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.11 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.13 |
embC | 4241024 | p.Val388Phe | missense_variant | 0.18 |
embC | 4241035 | c.1173G>C | synonymous_variant | 0.12 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.11 |
embC | 4241056 | c.1194C>A | synonymous_variant | 0.29 |
embC | 4241071 | c.1209C>A | synonymous_variant | 0.14 |
embC | 4241072 | p.Leu404Val | missense_variant | 0.14 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.17 |
embC | 4241109 | p.Ala416Gly | missense_variant | 0.17 |
embC | 4241116 | c.1254C>G | synonymous_variant | 0.17 |
embA | 4242361 | c.-872C>T | upstream_gene_variant | 0.25 |
embC | 4242977 | p.Leu1039Met | missense_variant | 0.22 |
embA | 4243066 | c.-167C>A | upstream_gene_variant | 0.5 |
embA | 4243197 | c.-36C>T | upstream_gene_variant | 0.29 |
embA | 4243293 | p.Gly21* | stop_gained | 0.25 |
embA | 4243301 | c.69G>T | synonymous_variant | 0.25 |
embA | 4243315 | p.Cys28Phe | missense_variant | 0.22 |
embA | 4243327 | p.Pro32Gln | missense_variant | 0.29 |
embA | 4244964 | p.Ala578Ser | missense_variant | 0.4 |
embA | 4244991 | p.Val587Phe | missense_variant | 0.33 |
embB | 4247624 | p.Pro371Thr | missense_variant | 0.25 |
embB | 4248475 | c.1962G>T | synonymous_variant | 0.15 |
embB | 4248619 | c.2106G>T | synonymous_variant | 0.17 |
embB | 4249166 | p.Gly885Cys | missense_variant | 0.25 |
embB | 4249734 | p.Pro1074Leu | missense_variant | 0.2 |
embB | 4249753 | p.Leu1080Phe | missense_variant | 0.25 |
aftB | 4268701 | p.Gly46Arg | missense_variant | 0.17 |
ubiA | 4269276 | p.Phe186Leu | missense_variant | 0.25 |
ubiA | 4269353 | p.Ala161Ser | missense_variant | 0.18 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.33 |
aftB | 4269378 | c.-542C>A | upstream_gene_variant | 0.22 |
aftB | 4269447 | c.-611C>A | upstream_gene_variant | 0.18 |
ubiA | 4269714 | p.Leu40Phe | missense_variant | 0.4 |
aftB | 4269816 | c.-980G>T | upstream_gene_variant | 0.29 |
ethA | 4326289 | c.1185C>A | synonymous_variant | 0.15 |
ethA | 4328261 | c.-788C>A | upstream_gene_variant | 0.18 |
ethA | 4328322 | c.-849G>T | upstream_gene_variant | 0.2 |