Run ID: ERR2228965
Sample name:
Date: 31-03-2023 16:28:32
Number of reads: 299839
Percentage reads mapped: 60.78
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6077 | p.Gly280Ser | missense_variant | 0.29 |
gyrB | 6468 | p.Ala410Gly | missense_variant | 0.29 |
gyrB | 7085 | p.Met616Val | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7409 | c.108C>T | synonymous_variant | 0.2 |
gyrA | 8870 | c.1569G>T | synonymous_variant | 0.15 |
fgd1 | 491295 | c.513C>A | synonymous_variant | 0.22 |
mshA | 575505 | p.His53Arg | missense_variant | 0.17 |
mshA | 576143 | p.Arg266Cys | missense_variant | 0.29 |
ccsA | 619817 | c.-74C>A | upstream_gene_variant | 0.4 |
ccsA | 619972 | p.Ala28Thr | missense_variant | 0.29 |
ccsA | 620052 | c.162G>A | synonymous_variant | 0.25 |
rpoB | 761549 | c.1743G>A | synonymous_variant | 0.25 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.22 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.22 |
rpoB | 762236 | c.2430G>T | synonymous_variant | 0.22 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.2 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.2 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.18 |
rpoB | 762616 | p.Gly937Asp | missense_variant | 1.0 |
rpoC | 762899 | c.-471G>T | upstream_gene_variant | 0.27 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.23 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.17 |
rpoC | 762959 | c.-411G>T | upstream_gene_variant | 0.17 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.17 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.17 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.18 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.14 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.4 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.5 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.42 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.69 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.69 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.58 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.27 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.27 |
rpoC | 763882 | p.Glu171Asp | missense_variant | 0.18 |
rpoC | 763886 | p.Arg173Trp | missense_variant | 0.18 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.13 |
rpoC | 764715 | c.1348delG | frameshift_variant | 0.13 |
rpoC | 764731 | c.1362G>T | synonymous_variant | 0.12 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.12 |
rpoC | 764868 | p.Arg500His | missense_variant | 0.13 |
rpoC | 765152 | p.Asp595Asn | missense_variant | 0.5 |
rpoC | 766808 | p.Val1147Met | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775938 | p.Ala848Val | missense_variant | 0.29 |
mmpL5 | 776780 | c.1701G>A | synonymous_variant | 0.25 |
mmpL5 | 776969 | p.Gln504His | missense_variant | 0.25 |
mmpL5 | 777937 | p.Val182Ile | missense_variant | 0.12 |
mmpL5 | 778448 | c.32delG | frameshift_variant | 0.2 |
mmpR5 | 779094 | p.Leu35Phe | missense_variant | 0.22 |
mmpL5 | 779169 | c.-689C>T | upstream_gene_variant | 0.33 |
mmpL5 | 779463 | c.-983G>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781781 | c.222G>C | synonymous_variant | 0.4 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.4 |
rplC | 800775 | c.-34G>A | upstream_gene_variant | 0.15 |
rplC | 800905 | p.Pro33Thr | missense_variant | 0.25 |
rplC | 800953 | p.Ala49Thr | missense_variant | 0.33 |
rplC | 801170 | p.Lys121Arg | missense_variant | 0.18 |
fbiC | 1302802 | c.-129G>T | upstream_gene_variant | 0.22 |
fbiC | 1303014 | c.84G>A | synonymous_variant | 0.22 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406209 | p.Ala378Ser | missense_variant | 0.15 |
Rv1258c | 1407152 | c.189C>A | synonymous_variant | 0.17 |
Rv1258c | 1407210 | p.Ala44Asp | missense_variant | 0.18 |
embR | 1416399 | p.Asp317His | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472522 | n.677T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472585 | n.740A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472744 | n.899A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473094 | n.1249T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473122 | n.1277T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475137 | n.1480A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475170 | n.1513A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475176 | n.1519G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475861 | n.2204A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476117 | n.2460G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.83 |
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 | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476493 | n.2836A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673803 | p.Arg122Trp | missense_variant | 0.15 |
fabG1 | 1673870 | p.Ser144Ile | missense_variant | 0.15 |
inhA | 1674537 | c.336C>A | synonymous_variant | 0.4 |
inhA | 1674730 | p.Arg177Ser | missense_variant | 0.22 |
inhA | 1674765 | c.564C>A | synonymous_variant | 0.22 |
rpsA | 1833397 | c.-145G>T | upstream_gene_variant | 0.33 |
rpsA | 1833599 | p.Glu20* | stop_gained | 0.13 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.33 |
rpsA | 1834012 | c.471G>A | synonymous_variant | 0.27 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.27 |
rpsA | 1834018 | c.477C>T | synonymous_variant | 0.27 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.25 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.21 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.21 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.21 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.29 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.33 |
rpsA | 1834828 | c.1287C>A | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918319 | p.Arg127Gln | missense_variant | 0.4 |
ndh | 2102228 | p.Ala272Asp | missense_variant | 0.2 |
katG | 2155852 | p.Ser87Leu | missense_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169430 | p.Gly395Ser | missense_variant | 0.17 |
PPE35 | 2170630 | c.-18C>A | upstream_gene_variant | 0.29 |
Rv1979c | 2221879 | p.Ala429Val | missense_variant | 0.14 |
Rv1979c | 2222132 | p.Gln345Lys | missense_variant | 0.18 |
Rv1979c | 2222192 | p.Arg325Trp | missense_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Val | missense_variant | 0.2 |
Rv1979c | 2222675 | p.Gly164* | stop_gained | 0.22 |
Rv1979c | 2222716 | p.Ala150Asp | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289584 | c.-343A>T | upstream_gene_variant | 0.22 |
kasA | 2518022 | c.-93C>G | upstream_gene_variant | 0.4 |
kasA | 2519317 | c.1203G>A | synonymous_variant | 0.15 |
eis | 2714802 | c.531G>T | synonymous_variant | 0.17 |
eis | 2714873 | p.Pro154Ser | missense_variant | 0.17 |
eis | 2715015 | c.318C>T | synonymous_variant | 0.33 |
folC | 2746586 | p.Arg338Leu | missense_variant | 0.2 |
folC | 2746831 | c.768G>T | synonymous_variant | 0.25 |
folC | 2747196 | p.Asp135Tyr | missense_variant | 0.67 |
pepQ | 2859364 | p.Pro352His | missense_variant | 0.22 |
pepQ | 2859422 | p.Arg333Cys | missense_variant | 0.4 |
pepQ | 2860469 | c.-51C>A | upstream_gene_variant | 0.22 |
ribD | 2987361 | p.Glu175* | stop_gained | 0.25 |
Rv2752c | 3065519 | p.Leu225Ile | missense_variant | 0.33 |
Rv2752c | 3065887 | c.304delG | frameshift_variant | 0.29 |
thyX | 3067383 | p.Asn188Ile | missense_variant | 0.33 |
thyX | 3067623 | p.Tyr108Cys | missense_variant | 0.22 |
thyX | 3067904 | c.42G>A | synonymous_variant | 0.33 |
thyA | 3073784 | p.Leu230Ile | missense_variant | 0.22 |
thyA | 3074630 | c.-159C>A | upstream_gene_variant | 0.17 |
ald | 3087131 | c.312C>T | synonymous_variant | 0.2 |
ald | 3087635 | c.816C>A | synonymous_variant | 0.5 |
fbiD | 3339499 | p.Ala128Ser | missense_variant | 0.22 |
fprA | 3474874 | p.Gly290Cys | missense_variant | 0.29 |
fprA | 3474877 | p.Arg291Cys | missense_variant | 0.29 |
fprA | 3475184 | p.Ala393Asp | missense_variant | 0.5 |
whiB7 | 3568870 | c.-191G>A | upstream_gene_variant | 0.15 |
Rv3236c | 3612056 | p.Leu354Ser | missense_variant | 0.2 |
fbiA | 3640571 | p.Val10Asp | missense_variant | 0.33 |
fbiA | 3640810 | p.Gln90Glu | missense_variant | 0.2 |
fbiA | 3640855 | p.Gly105Trp | missense_variant | 0.5 |
fbiB | 3642579 | p.Ile349Leu | missense_variant | 0.18 |
alr | 3840763 | p.Ala220Ser | missense_variant | 0.2 |
alr | 3841501 | c.-81G>T | upstream_gene_variant | 0.17 |
rpoA | 3878246 | p.Glu88* | stop_gained | 0.17 |
ddn | 3986948 | p.Glu35Asp | missense_variant | 0.22 |
ddn | 3987276 | p.Pro145Ala | missense_variant | 0.2 |
clpC1 | 4038460 | c.2245C>T | synonymous_variant | 0.22 |
clpC1 | 4038910 | p.Pro599Thr | missense_variant | 0.15 |
clpC1 | 4039672 | p.Val345Met | missense_variant | 0.22 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.22 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.2 |
clpC1 | 4039718 | c.987C>T | synonymous_variant | 0.18 |
clpC1 | 4040382 | p.Ile108Asn | missense_variant | 0.29 |
panD | 4044209 | p.Ser25Thr | missense_variant | 1.0 |
embC | 4239727 | c.-136A>T | upstream_gene_variant | 0.12 |
embC | 4240490 | p.Pro210Thr | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244634 | p.Val468Met | missense_variant | 0.67 |
embA | 4244739 | p.Tyr503Asn | missense_variant | 0.18 |
embA | 4244910 | p.Leu560Met | missense_variant | 0.67 |
embA | 4245163 | c.1934delC | frameshift_variant | 0.25 |
embA | 4245569 | p.Glu779Asp | missense_variant | 0.33 |
embA | 4245673 | p.Gly814Val | missense_variant | 0.29 |
embA | 4246477 | p.Pro1082His | missense_variant | 0.22 |
embB | 4246762 | c.249G>T | synonymous_variant | 0.12 |
embB | 4248163 | c.1650G>A | synonymous_variant | 0.14 |
embB | 4248172 | c.1659G>A | synonymous_variant | 0.15 |
embB | 4248834 | p.Trp774Leu | missense_variant | 0.29 |
embB | 4249606 | c.3093C>A | synonymous_variant | 0.67 |
aftB | 4268365 | p.Trp158Arg | missense_variant | 0.14 |
aftB | 4268400 | p.Ala146Gly | missense_variant | 0.11 |
aftB | 4268413 | p.Gly142Trp | missense_variant | 0.14 |
ethA | 4326315 | p.Thr387Ala | missense_variant | 0.18 |
ethA | 4326380 | p.Thr365Met | missense_variant | 0.25 |
ethA | 4327394 | p.Cys27Phe | missense_variant | 0.33 |
ethA | 4328064 | c.-591G>T | upstream_gene_variant | 0.22 |
ethA | 4328221 | c.-748A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338625 | c.-104C>A | upstream_gene_variant | 0.12 |
gid | 4407950 | p.Asp85Tyr | missense_variant | 0.17 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |