Run ID: ERR2843536
Sample name:
Date: 31-03-2023 23:53:52
Number of reads: 4767359
Percentage reads mapped: 85.02
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.11 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5626 | c.387C>T | synonymous_variant | 0.2 |
gyrB | 6423 | p.Trp395* | stop_gained | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7571 | c.270G>T | synonymous_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7640 | p.Gln113His | missense_variant | 0.2 |
gyrA | 7807 | p.Arg169Gln | missense_variant | 0.15 |
gyrA | 7835 | c.534A>T | synonymous_variant | 0.18 |
gyrA | 8554 | p.Arg418Leu | missense_variant | 0.18 |
gyrA | 8588 | c.1288delA | frameshift_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9567 | p.Asp756Tyr | missense_variant | 0.17 |
fgd1 | 491409 | c.627G>A | synonymous_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575704 | c.357T>G | synonymous_variant | 0.22 |
mshA | 575785 | c.438T>G | synonymous_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575951 | p.Gly202Trp | missense_variant | 0.2 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.21 |
ccsA | 620534 | p.Met215Thr | missense_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759852 | p.Ser16Cys | missense_variant | 0.13 |
rpoB | 759998 | p.Trp64Cys | missense_variant | 0.15 |
rpoB | 760790 | c.984C>T | synonymous_variant | 0.13 |
rpoB | 761572 | p.Pro589Arg | missense_variant | 0.18 |
rpoB | 761594 | c.1788C>T | synonymous_variant | 0.18 |
rpoB | 761856 | p.Val684Met | missense_variant | 0.15 |
rpoB | 761865 | p.Gly687Ser | missense_variant | 0.15 |
rpoB | 762993 | p.Gly1063Trp | missense_variant | 0.21 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765833 | p.Gly822Cys | missense_variant | 0.14 |
rpoC | 766859 | c.3490C>A | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775652 | c.2829C>T | synonymous_variant | 0.12 |
mmpL5 | 775726 | c.2755C>T | synonymous_variant | 0.12 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.15 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.15 |
mmpL5 | 775742 | c.2739C>T | synonymous_variant | 0.15 |
mmpL5 | 775747 | p.Met912Leu | missense_variant | 0.14 |
mmpL5 | 775834 | p.Ala883Thr | missense_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777815 | c.666C>A | synonymous_variant | 0.13 |
mmpL5 | 777991 | p.Glu164Lys | missense_variant | 0.15 |
mmpL5 | 778537 | c.-57G>A | upstream_gene_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304428 | c.1498C>A | synonymous_variant | 0.25 |
fbiC | 1304524 | p.Ala532Ser | missense_variant | 0.25 |
Rv1258c | 1406245 | p.Leu366Met | missense_variant | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416281 | p.Arg356Gln | missense_variant | 0.12 |
embR | 1416459 | p.Ser297Thr | missense_variant | 0.15 |
embR | 1416505 | c.843C>T | synonymous_variant | 0.14 |
embR | 1416906 | p.Pro148Ser | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471945 | n.100G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472100 | n.255T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472378 | n.533G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472423 | n.578G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472669 | n.824_825insTAG | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472677 | n.832C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472679 | n.834_835insAC | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472684 | n.841_846delGATCCG | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472708 | n.863T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472954 | n.1109T>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472992 | n.1147A>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473070 | n.1225G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473120 | n.1275C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473905 | n.248T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473926 | n.269G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474758 | n.1101G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475167 | n.1510T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475672 | n.2015C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475687 | n.2030C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475707 | n.2050T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475927 | n.2270G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673557 | p.His40Asn | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102039 | p.Gly335Val | missense_variant | 0.15 |
katG | 2154245 | p.Glu623Lys | missense_variant | 0.15 |
katG | 2154254 | p.Ser620Gly | missense_variant | 0.15 |
katG | 2154521 | p.Ala531Ser | missense_variant | 0.14 |
katG | 2154594 | c.1518G>A | synonymous_variant | 0.4 |
katG | 2154653 | p.Asp487His | missense_variant | 0.25 |
katG | 2154673 | p.Ala480Glu | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155355 | p.Arg253Trp | missense_variant | 0.17 |
katG | 2156369 | c.-258C>A | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169205 | p.Ile470Val | missense_variant | 0.14 |
PPE35 | 2169348 | p.Phe422Ser | missense_variant | 0.14 |
PPE35 | 2169375 | p.Asn413Thr | missense_variant | 0.11 |
Rv1979c | 2223211 | c.-47G>A | upstream_gene_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289243 | c.-2G>A | upstream_gene_variant | 0.14 |
kasA | 2518364 | p.Gln84* | stop_gained | 0.15 |
eis | 2715313 | p.Ser7Ile | missense_variant | 0.15 |
eis | 2715355 | c.-23G>A | upstream_gene_variant | 0.15 |
eis | 2715414 | c.-82C>A | upstream_gene_variant | 0.17 |
eis | 2715534 | c.-202C>T | upstream_gene_variant | 0.2 |
ahpC | 2726084 | c.-109C>T | upstream_gene_variant | 0.15 |
folC | 2747027 | p.Val191Gly | missense_variant | 0.25 |
folC | 2747134 | c.465C>T | synonymous_variant | 0.12 |
pepQ | 2859902 | p.Ser173Cys | missense_variant | 0.2 |
ribD | 2986886 | c.48G>A | synonymous_variant | 0.13 |
Rv2752c | 3064686 | p.Lys502Asn | missense_variant | 0.17 |
Rv2752c | 3065488 | p.Val235Asp | missense_variant | 0.18 |
thyA | 3073771 | p.Asp234Gly | missense_variant | 0.11 |
thyA | 3074442 | c.30C>T | synonymous_variant | 0.86 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086865 | p.Val16Met | missense_variant | 0.13 |
ald | 3087284 | c.465C>A | synonymous_variant | 0.17 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.3 |
Rv3083 | 3448889 | p.Arg129Leu | missense_variant | 0.21 |
Rv3083 | 3449069 | p.Ala189Glu | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474303 | c.297C>A | synonymous_variant | 0.15 |
fprA | 3475140 | c.1134C>A | synonymous_variant | 0.14 |
whiB7 | 3568427 | p.Arg85Ser | missense_variant | 0.13 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.27 |
whiB7 | 3568516 | p.Ala55Val | missense_variant | 0.17 |
Rv3236c | 3612068 | p.Gly350Val | missense_variant | 0.2 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641108 | p.Gly189Val | missense_variant | 0.13 |
fbiA | 3641113 | p.Glu191* | stop_gained | 0.14 |
fbiB | 3641334 | c.-201G>C | upstream_gene_variant | 0.18 |
fbiB | 3641657 | c.123C>A | synonymous_variant | 0.13 |
fbiB | 3641665 | p.Asp44Gly | missense_variant | 0.13 |
fbiB | 3641815 | p.Ile94Thr | missense_variant | 0.12 |
fbiB | 3642722 | c.1188C>T | synonymous_variant | 0.18 |
rpoA | 3878052 | c.456C>T | synonymous_variant | 0.17 |
rpoA | 3878613 | c.-113_-107delCAACCCA | upstream_gene_variant | 1.0 |
ddn | 3986713 | c.-131C>G | upstream_gene_variant | 0.15 |
clpC1 | 4038990 | p.Gly572Asp | missense_variant | 0.12 |
clpC1 | 4039004 | c.1701C>A | synonymous_variant | 0.18 |
clpC1 | 4039302 | p.Trp468Leu | missense_variant | 0.13 |
clpC1 | 4039988 | c.717C>A | synonymous_variant | 0.13 |
clpC1 | 4040852 | c.-148C>T | upstream_gene_variant | 0.29 |
embC | 4240192 | c.330C>A | synonymous_variant | 0.18 |
embC | 4241300 | p.Ala480Pro | missense_variant | 0.15 |
embC | 4241311 | c.1449C>A | synonymous_variant | 0.18 |
embC | 4241366 | c.1505delT | frameshift_variant | 0.22 |
embC | 4241468 | p.Ala536Thr | missense_variant | 0.18 |
embC | 4241745 | p.Phe628Ser | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245063 | c.1831C>T | synonymous_variant | 0.13 |
embA | 4245511 | p.Pro760Leu | missense_variant | 0.14 |
embB | 4247683 | c.1170C>T | synonymous_variant | 0.13 |
embB | 4247743 | c.1230C>T | synonymous_variant | 0.13 |
embB | 4248569 | p.Leu686Met | missense_variant | 0.14 |
embB | 4248613 | c.2100C>T | synonymous_variant | 0.13 |
embB | 4249105 | c.2592C>A | synonymous_variant | 0.2 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267985 | c.852C>T | synonymous_variant | 0.15 |
ethA | 4326145 | c.1329G>A | synonymous_variant | 0.13 |
ethA | 4326270 | p.Val402Phe | missense_variant | 0.13 |
ethA | 4326774 | p.Ala234Ser | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407643 | p.Arg187Lys | missense_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |