Run ID: SRR6982246
Sample name:
Date: 04-04-2023 18:31:42
Number of reads: 90801
Percentage reads mapped: 55.34
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7824 | p.Ala175Ile | missense_variant | 0.33 |
gyrA | 7832 | c.531G>C | synonymous_variant | 0.4 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.4 |
gyrA | 7837 | p.Gly179Ala | missense_variant | 0.4 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.33 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.33 |
gyrA | 8733 | p.Ile478Val | missense_variant | 0.5 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.29 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.29 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.62 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.57 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.47 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.47 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.5 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.5 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.5 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.5 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.5 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.44 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.4 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.4 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.4 |
rpoB | 761177 | c.1371G>C | synonymous_variant | 0.4 |
rpoB | 761180 | c.1374A>G | synonymous_variant | 0.4 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.4 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.4 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.4 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.33 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.4 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.4 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.4 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.4 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.4 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.5 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.5 |
rpoB | 761622 | p.Gln606Met | missense_variant | 0.4 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.4 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.67 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.67 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.67 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.67 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.67 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 0.67 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.67 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.67 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.67 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.6 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.6 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.75 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.75 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.75 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.75 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.75 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.75 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.6 |
rpoB | 762177 | p.Arg791Asp | missense_variant | 0.5 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.5 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.5 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.5 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.5 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.5 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.5 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.5 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.5 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.5 |
rpoB | 762275 | c.2469C>G | synonymous_variant | 0.5 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.5 |
rpoB | 762909 | p.Ile1035Leu | missense_variant | 0.22 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.3 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.3 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.3 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.25 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.27 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.27 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.27 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.27 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.27 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.3 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.3 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.3 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.3 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.3 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.25 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.25 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.27 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.27 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.27 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.27 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.3 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.3 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.3 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.27 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.33 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.43 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.43 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.43 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.43 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.5 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.43 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.43 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.43 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.5 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.5 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.5 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.5 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.43 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.43 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.43 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.43 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.4 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.18 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.2 |
rpoC | 764937 | p.Gln523Pro | missense_variant | 0.18 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776659 | p.Asp608Asn | missense_variant | 1.0 |
mmpL5 | 777690 | p.Asn264Ser | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472446 | n.601T>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472466 | n.621C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472673 | n.828T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472849 | n.1005delT | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472856 | n.1012_1015delAGGC | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472862 | n.1017T>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472863 | n.1018_1019insGCCC | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474651 | n.995delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474662 | n.1005C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474777 | n.1120T>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474896 | n.1239A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475324 | n.1667G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475601 | n.1945_1947delGGA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475607 | n.1950A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475609 | n.1952_1953insTG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475614 | n.1957A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475617 | n.1960C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475618 | n.1961C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475624 | n.1967G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475625 | n.1968G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475627 | n.1970G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475628 | n.1971G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475633 | n.1976G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475636 | n.1979A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475639 | n.1982C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475760 | n.2103_2104insACATTT | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475763 | n.2106C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475766 | n.2109G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476081 | n.2424A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476088 | n.2431A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476097 | n.2440C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476100 | n.2443A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476113 | n.2456T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476530 | n.2873C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.33 |
rpsA | 1833706 | c.165C>T | synonymous_variant | 0.43 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.38 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.55 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.55 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.6 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.6 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.6 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.6 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 0.6 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.6 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.6 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.6 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.44 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 0.44 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.4 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.4 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.44 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.44 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.44 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.44 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.44 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.38 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.25 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.25 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.29 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.29 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.22 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.22 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.22 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.3 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.38 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.29 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.25 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.25 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.25 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.25 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.25 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.25 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.25 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.25 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.25 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.29 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.67 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.67 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.67 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.67 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.67 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.67 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.67 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.67 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.67 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.67 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.67 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.67 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.73 |
rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.73 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.73 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.73 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.73 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.73 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.7 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.6 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.6 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.6 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.54 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.5 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.43 |
rpsA | 1834503 | p.Val321Ala | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917981 | c.42G>A | synonymous_variant | 1.0 |
ndh | 2103174 | c.-132G>C | upstream_gene_variant | 0.33 |
PPE35 | 2168501 | p.Phe704Leu | missense_variant | 1.0 |
PPE35 | 2170762 | c.-150C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2715231 | c.102C>T | synonymous_variant | 0.29 |
folC | 2746629 | p.Asp324Asn | missense_variant | 0.67 |
Rv2752c | 3066229 | c.-38T>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841250 | c.171C>T | synonymous_variant | 0.18 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.5 |
clpC1 | 4039647 | p.Glu353Pro | missense_variant | 0.5 |
clpC1 | 4039651 | p.Val352Leu | missense_variant | 0.5 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.5 |
clpC1 | 4039655 | c.1050G>C | synonymous_variant | 0.5 |
clpC1 | 4039661 | p.Gly348Ala | missense_variant | 0.5 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.5 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.67 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.67 |
clpC1 | 4039709 | p.Ile332Leu | missense_variant | 0.4 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.4 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.4 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.4 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.4 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.4 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.4 |
clpC1 | 4039754 | c.951G>C | synonymous_variant | 0.4 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.4 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.33 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.33 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.33 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.33 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.5 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.5 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.5 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.5 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.43 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.43 |
clpC1 | 4039858 | p.Ile283Val | missense_variant | 0.43 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4247121 | p.Ser203Leu | missense_variant | 1.0 |
embB | 4248651 | p.Phe713Ser | missense_variant | 0.25 |
aftB | 4267094 | c.1742delC | frameshift_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |