Run ID: ERR2228838
Sample name:
Date: 31-03-2023 16:22:35
Number of reads: 739177
Percentage reads mapped: 45.97
Strain: lineage4.8
Drug-resistance: RR-TB
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.27 | rifampicin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.62 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.5 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289234 | c.7delG | frameshift_variant | 0.17 | pyrazinamide, pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6834 | p.Asp532Ala | missense_variant | 0.2 |
gyrB | 7158 | c.1931_1933delCCG | disruptive_inframe_deletion | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.94 |
fgd1 | 491269 | p.Tyr163Asn | missense_variant | 0.25 |
fgd1 | 491315 | p.Gly178Ala | missense_variant | 0.29 |
fgd1 | 491558 | p.Lys259Thr | missense_variant | 0.25 |
mshA | 575512 | c.165A>C | synonymous_variant | 0.15 |
mshA | 576629 | p.Phe428Ile | missense_variant | 0.22 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.25 |
ccsA | 620132 | p.Leu81Arg | missense_variant | 0.33 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.12 |
rpoB | 761175 | c.1369C>T | synonymous_variant | 0.22 |
rpoB | 761180 | c.1374A>T | synonymous_variant | 0.2 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.22 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.27 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.19 |
rpoB | 761213 | c.1407G>T | synonymous_variant | 0.18 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.27 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.12 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.11 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.11 |
rpoB | 762071 | c.2265C>T | synonymous_variant | 0.19 |
rpoB | 762209 | c.2403C>T | synonymous_variant | 0.26 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.25 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.29 |
rpoB | 762236 | c.2430G>T | synonymous_variant | 0.26 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.23 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.29 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.27 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.25 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 0.17 |
rpoB | 762290 | c.2484C>T | synonymous_variant | 0.16 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.17 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.17 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.17 |
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 | 0.24 |
rpoC | 762959 | c.-411G>T | upstream_gene_variant | 0.24 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.25 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.24 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.18 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.19 |
rpoB | 763002 | c.3197dupA | frameshift_variant | 0.18 |
rpoB | 763006 | c.3201delC | frameshift_variant | 0.19 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.23 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.14 |
rpoC | 763339 | c.-31T>A | upstream_gene_variant | 0.2 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.28 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.38 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.36 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.39 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.39 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.36 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.33 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.38 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.33 |
rpoC | 763642 | c.273G>T | synonymous_variant | 0.29 |
rpoC | 763648 | c.279C>A | synonymous_variant | 0.22 |
rpoC | 763651 | c.282C>T | synonymous_variant | 0.15 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.12 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.12 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.11 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.11 |
rpoC | 763817 | p.Thr150Pro | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779614 | c.-709A>C | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303124 | p.Val65Gly | missense_variant | 0.27 |
fbiC | 1303243 | p.Cys105Ser | missense_variant | 0.16 |
fbiC | 1303666 | p.Thr246Pro | missense_variant | 0.31 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406509 | p.Tyr278Asp | missense_variant | 0.18 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472009 | n.164T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472522 | n.677T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472585 | n.740A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473094 | n.1249T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473122 | n.1277T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473862 | n.205C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473959 | n.302T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473964 | n.307T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474033 | n.376A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474166 | n.509G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474167 | n.510T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474467 | n.810A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474799 | n.1143delT | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474803 | n.1146_1147insA | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475510 | n.1853A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475516 | n.1859T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475517 | n.1860C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.81 |
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 | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475991 | n.2334T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475996 | n.2339T>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.28 |
fabG1 | 1673999 | p.Asp187Ala | missense_variant | 0.23 |
fabG1 | 1674038 | p.Gln200Leu | missense_variant | 0.23 |
inhA | 1674655 | p.Ser152Arg | missense_variant | 0.22 |
rpsA | 1833554 | p.Thr5Pro | missense_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1833985 | c.444G>T | synonymous_variant | 0.15 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.14 |
rpsA | 1834012 | c.471G>A | synonymous_variant | 0.17 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834018 | c.477C>T | synonymous_variant | 0.18 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.18 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.12 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.18 |
rpsA | 1834085 | p.Asn182Asp | missense_variant | 0.11 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.22 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.21 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.13 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.12 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.12 |
rpsA | 1834743 | p.Asn401Ile | missense_variant | 0.3 |
rpsA | 1834794 | p.Tyr418Ser | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154002 | p.Leu704Val | missense_variant | 0.22 |
katG | 2155549 | p.Val188Gly | missense_variant | 0.38 |
PPE35 | 2167681 | p.Ser978Pro | missense_variant | 0.25 |
PPE35 | 2167921 | p.Phe898Leu | missense_variant | 0.2 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.13 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170006 | p.Ile203Leu | missense_variant | 0.29 |
PPE35 | 2170631 | c.-19C>A | upstream_gene_variant | 0.14 |
Rv1979c | 2222918 | p.Thr83Pro | missense_variant | 0.17 |
Rv1979c | 2222986 | p.Val60Gly | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289264 | c.-23T>G | upstream_gene_variant | 0.43 |
kasA | 2518314 | p.Pro67Gln | missense_variant | 0.14 |
eis | 2714764 | p.Leu190Arg | missense_variant | 0.38 |
ahpC | 2726587 | p.Asp132Ala | missense_variant | 0.13 |
folC | 2746253 | p.Asp449Ala | missense_variant | 0.29 |
ribD | 2987010 | p.Thr58Pro | missense_variant | 0.13 |
Rv2752c | 3065350 | p.Val281Glu | missense_variant | 0.33 |
Rv2752c | 3065901 | c.291A>C | synonymous_variant | 0.23 |
thyX | 3067599 | p.Val116Gly | missense_variant | 0.31 |
thyX | 3067776 | p.Asn57Thr | missense_variant | 0.23 |
thyA | 3074154 | c.318T>A | synonymous_variant | 0.2 |
thyA | 3074318 | p.Phe52Ile | missense_variant | 0.33 |
fbiD | 3339703 | p.Thr196Pro | missense_variant | 0.33 |
Rv3083 | 3448341 | c.-163A>T | upstream_gene_variant | 0.4 |
whiB7 | 3568652 | p.Thr10Pro | missense_variant | 0.23 |
Rv3236c | 3612065 | p.Val351Gly | missense_variant | 0.18 |
Rv3236c | 3612185 | p.Phe311Cys | missense_variant | 0.18 |
Rv3236c | 3612974 | p.Ile48Ser | missense_variant | 0.2 |
fbiB | 3641953 | p.Leu140Arg | missense_variant | 0.25 |
fbiB | 3642280 | p.Leu249Arg | missense_variant | 0.27 |
fbiB | 3642471 | p.Met313Leu | missense_variant | 0.21 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.21 |
rpoA | 3878408 | p.Leu34Met | missense_variant | 0.2 |
rpoA | 3878415 | c.93C>A | synonymous_variant | 0.21 |
rpoA | 3878470 | p.Val13Ala | missense_variant | 0.15 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.57 |
clpC1 | 4038956 | c.1749T>G | synonymous_variant | 0.4 |
embC | 4241043 | p.Asn394Thr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243993 | p.Asp254Ala | missense_variant | 0.23 |
embB | 4246761 | p.Val83Gly | missense_variant | 0.19 |
embB | 4247470 | p.Tyr319* | stop_gained | 0.22 |
aftB | 4267010 | p.Glu609Asp | missense_variant | 0.22 |
aftB | 4268370 | p.Val156Gly | missense_variant | 0.29 |
aftB | 4268603 | c.234C>T | synonymous_variant | 0.33 |
aftB | 4268808 | p.Val10Gly | missense_variant | 0.29 |
aftB | 4268861 | c.-25T>G | upstream_gene_variant | 0.2 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407813 | c.390C>T | synonymous_variant | 0.18 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |