Run ID: ERR4818624
Sample name:
Date: 01-04-2023 15:39:45
Number of reads: 1681092
Percentage reads mapped: 63.57
Strain: lineage4.3.4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.24 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.18 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.11 |
gyrA | 6535 | c.-767C>G | upstream_gene_variant | 0.12 |
gyrA | 6541 | c.-761C>T | upstream_gene_variant | 0.12 |
gyrB | 6542 | p.Ile435Leu | missense_variant | 0.12 |
gyrA | 6550 | c.-752A>T | upstream_gene_variant | 0.13 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.13 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.17 |
gyrA | 6580 | c.-722C>G | upstream_gene_variant | 0.11 |
gyrB | 6582 | p.Thr448Lys | missense_variant | 0.11 |
gyrB | 6590 | p.Arg451Ser | missense_variant | 0.11 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.12 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.12 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.14 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.14 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.14 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.13 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.12 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.15 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.12 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.12 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.12 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.12 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.12 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.12 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.12 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.19 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.28 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.19 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.17 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.23 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 0.18 |
rpoB | 762077 | c.2271G>A | synonymous_variant | 0.16 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.17 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.21 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.2 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.22 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.24 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.22 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.22 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 0.23 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.25 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.24 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.29 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.24 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.23 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.11 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.26 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.12 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.12 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.15 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.15 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.15 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.12 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.11 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.11 |
rpoB | 762350 | c.2544C>G | synonymous_variant | 0.11 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.18 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.16 |
rpoC | 762920 | c.-450C>G | upstream_gene_variant | 0.15 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.15 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.21 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.24 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.13 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.21 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.17 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.21 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.25 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.26 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.23 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.23 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.23 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.2 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.24 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.26 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.21 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.12 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.16 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.23 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.23 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.16 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.15 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.15 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.13 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.11 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.16 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.15 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.11 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.11 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.12 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.13 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.12 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.12 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.13 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.12 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.12 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.11 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.11 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.11 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.14 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.14 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.13 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.18 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.19 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 0.18 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.22 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.23 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.19 |
rpoC | 764858 | p.Leu497Met | missense_variant | 0.19 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.15 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.95 |
rpoC | 765814 | c.2445A>T | synonymous_variant | 0.12 |
rpoC | 765817 | c.2448G>C | synonymous_variant | 0.11 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.11 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.13 |
rpoC | 765832 | c.2463G>A | synonymous_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.14 |
rpoC | 765865 | c.2496C>T | synonymous_variant | 0.14 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.15 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.15 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 0.12 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.12 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.12 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 0.11 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.17 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.13 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.26 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.29 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.21 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.26 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.25 |
rpoC | 766429 | c.3061_3062insCGG | disruptive_inframe_insertion | 0.27 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 0.27 |
rpoC | 766456 | c.3087C>T | synonymous_variant | 0.27 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.25 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.13 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 0.14 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.1 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.13 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.18 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.15 |
rpoC | 767041 | c.3672G>C | synonymous_variant | 0.19 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.18 |
rpoC | 767056 | c.3687C>G | synonymous_variant | 0.13 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.12 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.11 |
rpoC | 767066 | c.3697C>T | synonymous_variant | 0.11 |
rpoC | 767071 | c.3702C>G | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.12 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.11 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.12 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.12 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.12 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.12 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.11 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.12 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.14 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471978 | n.133C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472580 | n.735C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472971 | n.1126G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473717 | n.60G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473811 | n.154C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473815 | n.158T>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475990 | n.2333G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476049 | n.2392C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476524 | n.2867delC | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1833571 | c.30A>G | synonymous_variant | 0.13 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.13 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.12 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.12 |
rpsA | 1833607 | c.66T>C | synonymous_variant | 0.15 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.17 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.17 |
rpsA | 1833652 | c.111C>T | synonymous_variant | 0.11 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.13 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.12 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.14 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.13 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.12 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.12 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.12 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.16 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.16 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.16 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.16 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.14 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.14 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.14 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 0.13 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.15 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.21 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.19 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.24 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.19 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.16 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.17 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.2 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.21 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.2 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.27 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.26 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.24 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.16 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.12 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.17 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.21 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.21 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.15 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.15 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.12 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.12 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.12 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.11 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.14 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.16 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.15 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.11 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.12 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.11 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.11 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.14 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155766 | p.His116Asp | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519075 | p.Ala321Ser | missense_variant | 0.11 |
folC | 2746761 | p.Gln280Lys | missense_variant | 0.1 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.12 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.11 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.13 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.12 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.12 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.15 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.12 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.11 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.12 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.12 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.13 |
clpC1 | 4039046 | c.1659C>T | synonymous_variant | 0.19 |
clpC1 | 4039070 | c.1635G>C | synonymous_variant | 0.17 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.18 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.16 |
clpC1 | 4039082 | c.1623C>T | synonymous_variant | 0.16 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.17 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.17 |
clpC1 | 4039100 | c.1605C>T | synonymous_variant | 0.17 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.11 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.11 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.12 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.12 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.13 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.12 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.12 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.14 |
clpC1 | 4039223 | c.1482C>T | synonymous_variant | 0.12 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 0.12 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.12 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.11 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.15 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.16 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.13 |
clpC1 | 4039571 | c.1134G>C | synonymous_variant | 0.12 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.12 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.13 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 0.12 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.14 |
clpC1 | 4039636 | p.Glu357Lys | missense_variant | 0.12 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.19 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.19 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.16 |
clpC1 | 4039688 | c.1017G>A | synonymous_variant | 0.18 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.24 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.17 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.13 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.2 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.14 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.14 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.13 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.15 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.15 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.13 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.13 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.13 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.11 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.16 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.15 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.13 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.13 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.13 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.12 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.12 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.12 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.12 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.12 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.11 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.13 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.17 |
clpC1 | 4040124 | p.Glu194Ser | missense_variant | 0.13 |
clpC1 | 4040138 | c.567G>C | synonymous_variant | 0.17 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.17 |
clpC1 | 4040158 | p.Met183Leu | missense_variant | 0.16 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.13 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.13 |
clpC1 | 4040166 | p.Ala180Gln | missense_variant | 0.14 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.13 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |