Run ID: ERR3445487
Sample name:
Date: 01-04-2023 02:12:51
Number of reads: 1199657
Percentage reads mapped: 40.8
Strain: La1.7.X-unk4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 0.99 |
La1.7 | M.bovis | None | None | 1.0 |
La1.7.X-unk4 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.68 | streptomycin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>T | synonymous_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.16 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.16 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.16 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.12 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.17 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.17 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.16 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.19 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.14 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.2 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.16 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.16 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.22 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.16 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.18 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.3 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.32 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.29 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.29 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.32 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.35 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.36 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.32 |
rpoB | 761613 | p.Ala603Ser | missense_variant | 0.28 |
rpoB | 761631 | p.Ala609Ser | missense_variant | 0.28 |
rpoB | 761643 | p.Val613Ile | missense_variant | 0.27 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.34 |
rpoB | 761650 | p.Ser615Asn | missense_variant | 0.27 |
rpoB | 761654 | p.Glu616Asp | missense_variant | 0.28 |
rpoB | 761663 | c.1857G>C | synonymous_variant | 0.24 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.31 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.19 |
rpoB | 761682 | c.1876C>T | synonymous_variant | 0.21 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.18 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.17 |
rpoB | 761967 | p.Glu721Gln | missense_variant | 0.16 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.16 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.16 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.14 |
rpoB | 762009 | p.Leu735Val | missense_variant | 0.13 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.13 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.14 |
rpoB | 762024 | p.Val740Leu | missense_variant | 0.16 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.16 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.22 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.19 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.21 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.24 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.27 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.23 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.27 |
rpoB | 762117 | c.2311_2312delTCinsAG | synonymous_variant | 0.21 |
rpoB | 762126 | p.Val774Met | missense_variant | 0.3 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.3 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.29 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.29 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.27 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.28 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.25 |
rpoB | 762177 | p.Arg791Ser | missense_variant | 0.24 |
rpoB | 762180 | p.Asp792Asn | missense_variant | 0.23 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.25 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.26 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.23 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.23 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.22 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.23 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.2 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.2 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.18 |
rpoB | 762387 | p.Glu861Gln | missense_variant | 0.12 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.15 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.14 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.14 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.21 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.21 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.21 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.22 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.27 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.33 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.38 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.4 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.46 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.45 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.35 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.35 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.35 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.23 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.2 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.22 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.21 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.24 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.26 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.24 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.32 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.28 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.23 |
rpoB | 763077 | p.Val1091Leu | missense_variant | 0.2 |
rpoC | 763082 | c.-288C>A | upstream_gene_variant | 0.2 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.2 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.34 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.33 |
rpoC | 763496 | p.Lys43Arg | missense_variant | 0.31 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.48 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.48 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.49 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.53 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.6 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.61 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.62 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.49 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.51 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.48 |
rpoC | 763648 | c.279C>A | synonymous_variant | 0.46 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.41 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.41 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.19 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.19 |
rpoC | 764326 | c.957G>C | synonymous_variant | 0.23 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.36 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.33 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.34 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.34 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.32 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.38 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.31 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.36 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.42 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.36 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.38 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.38 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.38 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.33 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.36 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.36 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.31 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.42 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.38 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.37 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.29 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.31 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.32 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.38 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.39 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.36 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.33 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.5 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.47 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.47 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.48 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.59 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.58 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.59 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.6 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.61 |
rpoC | 764650 | c.1281G>A | synonymous_variant | 0.62 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.6 |
rpoC | 764665 | c.1296C>T | synonymous_variant | 0.6 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.54 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.49 |
rpoC | 764714 | p.Leu449Ile | missense_variant | 0.49 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.49 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.48 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.49 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.46 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.39 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.38 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.32 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.36 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.29 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.31 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.26 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.23 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.18 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.22 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.22 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.22 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.21 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.21 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.23 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.21 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.2 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.22 |
rpsL | 781841 | c.282C>A | synonymous_variant | 0.19 |
rpsL | 781856 | c.297C>T | synonymous_variant | 0.18 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.18 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.18 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.18 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.19 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
embR | 1416666 | p.Tyr228His | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472114 | n.269A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472583 | n.738T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472585 | n.740A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472791 | n.946G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473065 | n.1220C>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474166 | n.509G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474534 | n.877G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474800 | n.1143T>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474801 | n.1144G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474917 | n.1260G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474934 | n.1277C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474935 | n.1278A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475080 | n.1423G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475479 | n.1822C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475602 | n.1945G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475880 | n.2223C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475881 | n.2224T>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475882 | n.2225C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476248 | n.2591G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476259 | n.2602C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.39 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.17 |
rpsA | 1833649 | c.108C>T | synonymous_variant | 0.16 |
rpsA | 1833661 | p.Glu40Asp | missense_variant | 0.2 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.21 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.18 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.19 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.19 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.23 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.26 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.26 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.26 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.26 |
rpsA | 1833739 | c.198C>G | synonymous_variant | 0.22 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.22 |
rpsA | 1833770 | p.Asn77His | missense_variant | 0.19 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.12 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.13 |
rpsA | 1833835 | c.294C>G | synonymous_variant | 0.13 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.13 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.16 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.24 |
rpsA | 1833859 | c.318C>G | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.29 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.26 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.25 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.28 |
rpsA | 1833904 | p.Glu121Asp | missense_variant | 0.26 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.27 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.28 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.26 |
rpsA | 1833920 | p.Lys127Glu | missense_variant | 0.27 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.36 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.42 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.36 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.4 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.34 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.38 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.34 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.31 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.35 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.31 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.29 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.3 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.27 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.29 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.27 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.27 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.27 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.27 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.27 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.29 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.17 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.15 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.17 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.21 |
rpsA | 1834240 | c.699T>A | synonymous_variant | 0.24 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.25 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.26 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.34 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.35 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.39 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.46 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.47 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.45 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.42 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.35 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.31 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.33 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.36 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.35 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.33 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.4 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.43 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.45 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.46 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.44 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.5 |
rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.47 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.52 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.45 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.43 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.38 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.38 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.35 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.46 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.42 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.29 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.16 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.16 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.16 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.17 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.18 |
rpsA | 1834654 | c.1113G>A | synonymous_variant | 0.15 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
folC | 2746171 | c.1428G>A | synonymous_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.14 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.14 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.13 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.13 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.14 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.19 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.19 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.19 |
clpC1 | 4039588 | p.Ser373Thr | missense_variant | 0.16 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.17 |
clpC1 | 4039616 | c.1089G>T | synonymous_variant | 0.23 |
clpC1 | 4039631 | p.Ile358Met | missense_variant | 0.17 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.14 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 0.13 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.13 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.615T>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.15 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.12 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.17 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.15 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.14 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.18 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.18 |
clpC1 | 4040429 | c.274_276delTTGinsCTC | synonymous_variant | 0.16 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 0.16 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.18 |
clpC1 | 4040456 | c.249C>T | synonymous_variant | 0.14 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.17 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.16 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.19 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 0.14 |
clpC1 | 4040480 | c.223_225delTCTinsAGC | synonymous_variant | 0.2 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 0.98 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267034 | c.1803C>T | synonymous_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |