Run ID: SRR13423629
Sample name:
Date: 03-04-2023 08:54:33
Number of reads: 1618033
Percentage reads mapped: 48.88
Strain: lineage2.2.1
Drug-resistance: MDR-TB
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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.8 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288750 | c.491_492insA | frameshift_variant | 0.27 | pyrazinamide |
pncA | 2288757 | p.Gly162Asp | missense_variant | 0.17 | pyrazinamide |
pncA | 2288954 | c.287delA | frameshift_variant | 0.76 | pyrazinamide, pyrazinamide |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5119 | c.-121T>C | upstream_gene_variant | 1.0 |
gyrB | 5545 | c.306A>G | synonymous_variant | 0.13 |
gyrB | 5711 | p.Leu158Phe | missense_variant | 0.12 |
gyrB | 5753 | c.516delG | frameshift_variant | 0.15 |
gyrA | 6928 | c.-374G>A | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7852 | p.Gly184Asp | missense_variant | 0.12 |
gyrA | 8201 | c.900C>A | synonymous_variant | 0.22 |
gyrA | 8320 | p.Ser340Ile | missense_variant | 0.22 |
gyrA | 8357 | c.1056G>A | synonymous_variant | 0.14 |
gyrA | 8754 | c.1456delA | frameshift_variant | 0.11 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9639 | p.Gly780Arg | missense_variant | 0.17 |
fgd1 | 490960 | p.Ala60Thr | missense_variant | 0.11 |
fgd1 | 491257 | p.Gly159Cys | missense_variant | 0.12 |
fgd1 | 491637 | c.855C>A | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759914 | c.108T>A | synonymous_variant | 0.11 |
rpoB | 760480 | p.Arg225Leu | missense_variant | 0.13 |
rpoB | 761020 | p.Ala405Val | missense_variant | 0.12 |
rpoB | 761418 | p.Ala538Ser | missense_variant | 0.85 |
rpoC | 762785 | c.-585C>T | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763359 | c.-11A>G | upstream_gene_variant | 0.22 |
rpoC | 764040 | p.Ser224Ile | missense_variant | 0.14 |
rpoC | 764143 | c.774G>T | synonymous_variant | 0.11 |
rpoC | 765358 | p.Met663Ile | missense_variant | 0.13 |
rpoC | 766202 | p.Gly945Ser | missense_variant | 1.0 |
rpoC | 766860 | p.Arg1164Gln | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776986 | c.1493_1494delCG | frameshift_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781930 | p.Gly124Asp | missense_variant | 0.12 |
rplC | 801392 | c.587delG | frameshift_variant | 0.18 |
fbiC | 1303002 | c.76_80delTTGCG | frameshift_variant | 0.11 |
fbiC | 1303395 | p.Trp155* | stop_gained | 0.13 |
fbiC | 1305347 | p.Asp806Gly | missense_variant | 0.12 |
fbiC | 1305390 | c.2462delG | frameshift_variant | 0.12 |
Rv1258c | 1406253 | p.Gly363Val | missense_variant | 0.97 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416593 | p.Glu252Gly | missense_variant | 0.12 |
embR | 1416676 | c.672G>A | synonymous_variant | 0.12 |
embR | 1416859 | c.489C>A | synonymous_variant | 0.17 |
atpE | 1460897 | c.-147delT | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472669 | n.824_825insTGGA | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473317 | n.1474_1475dupCG | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474747 | n.1090C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474779 | n.1122G>A | 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 | 0.33 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474797 | n.1140G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474799 | n.1142G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474801 | n.1144G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475174 | n.1520delG | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475541 | n.1884G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475626 | n.1972delG | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475707 | n.2050T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475752 | n.2095C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475776 | n.2119G>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476071 | n.2414C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674210 | c.9A>C | synonymous_variant | 0.87 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918042 | p.Asp35Tyr | missense_variant | 0.14 |
ndh | 2101727 | p.Arg439Leu | missense_variant | 0.29 |
ndh | 2101890 | c.1152delC | frameshift_variant | 0.14 |
ndh | 2102243 | p.Arg267Gln | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155965 | p.His49Gln | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168022 | p.Leu864Pro | missense_variant | 0.11 |
PPE35 | 2170031 | c.581delG | frameshift_variant | 0.12 |
PPE35 | 2170638 | c.-26A>G | upstream_gene_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518526 | c.416delC | frameshift_variant | 0.2 |
kasA | 2518615 | c.504_505dupGT | frameshift_variant | 0.12 |
folC | 2747776 | c.-178G>A | upstream_gene_variant | 0.12 |
pepQ | 2859756 | c.663C>T | synonymous_variant | 0.12 |
pepQ | 2859855 | c.564G>A | synonymous_variant | 0.18 |
pepQ | 2860423 | c.-5G>C | upstream_gene_variant | 0.1 |
ribD | 2987398 | c.563_564delGC | frameshift_variant | 0.15 |
Rv2752c | 3064527 | c.1665C>A | synonymous_variant | 0.29 |
Rv2752c | 3064883 | p.Ser437Gly | missense_variant | 0.14 |
Rv2752c | 3065362 | p.Gly277Asp | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087185 | c.367delG | frameshift_variant | 0.1 |
ald | 3087926 | c.1107G>A | synonymous_variant | 0.13 |
fbiD | 3339377 | p.Asp87Gly | missense_variant | 0.11 |
fbiD | 3339385 | p.Asp90Tyr | missense_variant | 0.16 |
Rv3083 | 3448728 | c.225C>A | synonymous_variant | 0.12 |
Rv3083 | 3449226 | p.Glu241Asp | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474451 | p.Arg149Trp | missense_variant | 0.2 |
fprA | 3474586 | c.581delT | frameshift_variant | 0.13 |
fprA | 3474620 | p.Ala205Asp | missense_variant | 0.15 |
whiB7 | 3568746 | c.-70_-68delACC | upstream_gene_variant | 0.11 |
Rv3236c | 3612013 | p.Ile368Met | missense_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640763 | p.Asp74Gly | missense_variant | 0.11 |
fbiA | 3640849 | p.Glu103* | stop_gained | 0.14 |
fbiB | 3641274 | c.-261G>A | upstream_gene_variant | 0.12 |
fbiB | 3642132 | p.Ala200Thr | missense_variant | 0.15 |
rpoA | 3877969 | p.Ala180Val | missense_variant | 1.0 |
rpoA | 3878389 | p.Arg40His | missense_variant | 0.17 |
rpoA | 3878614 | c.-108_-107insC | upstream_gene_variant | 0.2 |
panD | 4044313 | c.-32C>T | upstream_gene_variant | 0.2 |
embC | 4240047 | p.Pro62Leu | missense_variant | 0.11 |
embC | 4242251 | p.Asp797Tyr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242680 | p.Ala940Thr | missense_variant | 0.17 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243550 | p.Phe106Leu | missense_variant | 0.12 |
embA | 4243965 | p.Arg245Trp | missense_variant | 0.12 |
embA | 4245583 | p.Asp784Gly | missense_variant | 0.12 |
embB | 4246130 | c.-384T>C | upstream_gene_variant | 0.17 |
embB | 4246559 | c.50delT | frameshift_variant | 0.17 |
embB | 4247334 | p.Arg274His | missense_variant | 0.15 |
embB | 4247894 | p.Pro461Ala | missense_variant | 1.0 |
embB | 4249377 | p.Leu955Pro | missense_variant | 0.1 |
aftB | 4267279 | p.Arg520Trp | missense_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268088 | c.748delT | frameshift_variant | 0.18 |
aftB | 4269533 | c.-697C>T | upstream_gene_variant | 0.18 |
ubiA | 4269733 | p.Ala34Val | missense_variant | 0.12 |
ethA | 4326486 | p.Gly330Ser | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338644 | c.-123C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |