Run ID: ERR2228899
Sample name:
Date: 31-03-2023 16:25:17
Number of reads: 442692
Percentage reads mapped: 65.67
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.15 | rifampicin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.83 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.92 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6015 | p.Asp259Gly | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8378 | p.Asp359Glu | missense_variant | 0.14 |
gyrA | 8492 | c.1191G>A | synonymous_variant | 0.13 |
gyrA | 9056 | c.1755C>A | synonymous_variant | 0.14 |
fgd1 | 490759 | c.-24A>G | upstream_gene_variant | 0.14 |
mshA | 576635 | c.1291delG | frameshift_variant | 0.13 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.23 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.23 |
rpoB | 761160 | c.1354C>T | synonymous_variant | 0.23 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.21 |
rpoB | 761175 | c.1369C>T | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>T | synonymous_variant | 0.17 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.12 |
rpoB | 761213 | c.1407G>T | synonymous_variant | 0.22 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.17 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.16 |
rpoB | 761246 | c.1440C>T | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.19 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.19 |
rpoB | 761516 | c.1710G>C | synonymous_variant | 0.22 |
rpoB | 761592 | c.1788delC | frameshift_variant | 0.2 |
rpoB | 761711 | c.1905C>A | synonymous_variant | 0.25 |
rpoB | 762197 | c.2391C>T | synonymous_variant | 0.17 |
rpoB | 762198 | p.Gly798Cys | missense_variant | 0.17 |
rpoB | 762209 | c.2403C>T | synonymous_variant | 0.17 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.31 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.44 |
rpoB | 762236 | c.2430G>T | synonymous_variant | 0.44 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.45 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.27 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.27 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.13 |
rpoB | 762429 | p.Asp875Ile | missense_variant | 0.2 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.13 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.13 |
rpoC | 762899 | c.-471G>T | upstream_gene_variant | 0.19 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.21 |
rpoB | 762930 | p.Pro1042Thr | missense_variant | 0.17 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.15 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.2 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.17 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.17 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.16 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.15 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.13 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.13 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.12 |
rpoC | 764896 | c.1527C>T | synonymous_variant | 0.12 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.2 |
rpoC | 765973 | c.2604C>G | synonymous_variant | 0.25 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.25 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776610 | p.Met624Thr | missense_variant | 0.12 |
mmpL5 | 778963 | c.-483G>T | upstream_gene_variant | 0.17 |
mmpR5 | 779109 | p.Leu40Phe | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.12 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.21 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.23 |
rplC | 800890 | p.Val28Met | missense_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304083 | p.Gly385Cys | missense_variant | 0.4 |
embR | 1417057 | c.291G>A | synonymous_variant | 0.14 |
embR | 1417138 | c.210G>T | synonymous_variant | 0.14 |
embR | 1417501 | c.-154A>G | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471926 | n.81C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471930 | n.85G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471936 | n.91A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471993 | n.149_150delGC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472009 | n.164T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472085 | n.240C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472522 | n.677T>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472585 | n.740A>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472837 | n.992C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473094 | n.1249T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473122 | n.1277T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473347 | n.1502C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473445 | n.-213G>T | upstream_gene_variant | 0.33 |
rrl | 1473862 | n.205C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474166 | n.509G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474167 | n.510T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474269 | n.612C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474287 | n.631_649delCCTTTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474467 | n.810A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474799 | n.1143delT | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474803 | n.1146_1147insA | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475991 | n.2334T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475996 | n.2339T>G | non_coding_transcript_exon_variant | 1.0 |
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 | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476288 | n.2635_2643delGCACCCCCG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476301 | n.2644_2645insCGGTGGCTT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476316 | n.2659G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476385 | n.2731delT | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476523 | n.2866T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476546 | n.2889C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476564 | n.2907G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
rpsA | 1833985 | c.444G>T | synonymous_variant | 0.17 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.19 |
rpsA | 1833997 | c.456G>T | synonymous_variant | 0.19 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.2 |
rpsA | 1834012 | c.471G>A | synonymous_variant | 0.12 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.12 |
rpsA | 1834018 | c.477C>T | synonymous_variant | 0.12 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.11 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.11 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.11 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.11 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.14 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.14 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.14 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.14 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.12 |
tlyA | 1917747 | c.-193A>T | upstream_gene_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101853 | p.Leu397Arg | missense_variant | 0.22 |
katG | 2154698 | c.1414C>T | synonymous_variant | 0.15 |
katG | 2156392 | c.-281C>A | upstream_gene_variant | 0.22 |
PPE35 | 2167916 | c.2696delT | frameshift_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.21 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.21 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.18 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.23 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.2 |
PPE35 | 2169322 | c.1291T>C | synonymous_variant | 0.12 |
PPE35 | 2169323 | c.1290C>G | synonymous_variant | 0.12 |
PPE35 | 2169326 | c.1287C>T | synonymous_variant | 0.12 |
PPE35 | 2169596 | p.Phe339Val | missense_variant | 0.12 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.12 |
PPE35 | 2169605 | p.Asn336Thr | missense_variant | 0.12 |
PPE35 | 2169611 | c.1002C>G | synonymous_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.17 |
PPE35 | 2169990 | p.Gly208Ala | missense_variant | 0.18 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289426 | c.-185G>T | upstream_gene_variant | 0.14 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.27 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.27 |
kasA | 2519052 | p.Thr313Met | missense_variant | 0.33 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.29 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.29 |
eis | 2714504 | p.His277Asn | missense_variant | 0.2 |
pepQ | 2860203 | p.Glu72Asp | missense_variant | 0.22 |
pepQ | 2860594 | c.-176C>A | upstream_gene_variant | 0.2 |
ribD | 2986719 | c.-120G>A | upstream_gene_variant | 0.33 |
Rv2752c | 3064945 | p.Pro416Gln | missense_variant | 0.12 |
Rv2752c | 3065485 | p.Ala236Val | missense_variant | 0.22 |
Rv2752c | 3066074 | p.Leu40Val | missense_variant | 0.12 |
Rv2752c | 3066110 | p.Gly28Ser | missense_variant | 0.12 |
Rv2752c | 3066999 | c.-808C>A | upstream_gene_variant | 0.15 |
thyX | 3067401 | p.Arg182Pro | missense_variant | 0.4 |
ald | 3087301 | p.Gly161Val | missense_variant | 0.14 |
ald | 3087344 | c.525C>A | synonymous_variant | 0.18 |
Rv3083 | 3448414 | c.-90T>C | upstream_gene_variant | 0.14 |
fprA | 3474987 | c.981G>T | synonymous_variant | 0.25 |
whiB7 | 3568462 | p.Gln73Arg | missense_variant | 0.15 |
alr | 3840243 | p.Ser393Asn | missense_variant | 0.18 |
alr | 3840258 | p.Tyr388Phe | missense_variant | 0.18 |
alr | 3840769 | p.Phe218Leu | missense_variant | 0.29 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.18 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.12 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.13 |
rpoA | 3878492 | p.Arg6Cys | missense_variant | 0.15 |
clpC1 | 4039624 | p.Gly361Cys | missense_variant | 0.13 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243582 | p.Ala117Val | missense_variant | 0.33 |
embA | 4245010 | p.Ala593Asp | missense_variant | 0.12 |
embA | 4245269 | p.Asn679Lys | missense_variant | 0.25 |
embA | 4245488 | c.2256G>T | synonymous_variant | 0.29 |
embB | 4246154 | c.-360G>A | upstream_gene_variant | 0.25 |
embB | 4247907 | p.Ile465Asn | missense_variant | 0.4 |
embB | 4248154 | c.1641G>C | synonymous_variant | 0.17 |
embB | 4248507 | p.Gly665Val | missense_variant | 0.12 |
ethA | 4327467 | p.Glu3Lys | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407997 | p.Gly69Val | missense_variant | 0.17 |
gid | 4408313 | c.-111A>G | upstream_gene_variant | 0.4 |
gid | 4408375 | c.-173G>A | upstream_gene_variant | 0.25 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |