Run ID: ERR4821272
Sample name:
Date: 01-04-2023 17:09:42
Number of reads: 1733787
Percentage reads mapped: 74.74
Strain: lineage4.1.2.1
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.19 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.75 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.48 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.22 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.15 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.18 |
rpoB | 761037 | c.1231_1233delTTGinsCTC | synonymous_variant | 0.17 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.16 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.17 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.17 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.15 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 0.15 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.16 |
rpoB | 761111 | c.1305C>T | synonymous_variant | 0.17 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.19 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.2 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.2 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.18 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761156 | c.1350G>T | synonymous_variant | 0.19 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.11 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.14 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.14 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761255 | c.1449T>C | synonymous_variant | 0.11 |
rpoB | 761973 | p.His723Tyr | missense_variant | 0.12 |
rpoB | 761980 | p.Tyr725Phe | missense_variant | 0.12 |
rpoB | 761987 | c.2181C>T | synonymous_variant | 0.13 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.12 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.12 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.12 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.12 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.12 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.11 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.12 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.12 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.14 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.14 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.14 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.15 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.18 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.2 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.11 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.11 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.12 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.12 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.12 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.14 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.15 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.17 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.11 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.11 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.17 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.17 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.2 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.18 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.19 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.18 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.17 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.16 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.15 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.16 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.16 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.15 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.14 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.15 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.15 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.15 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.15 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.14 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.12 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.13 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.13 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.12 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.12 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.12 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.12 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.13 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.19 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.19 |
rpoC | 764679 | p.Lys437Ser | missense_variant | 0.18 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.19 |
rpoC | 764690 | p.Cys441Ala | missense_variant | 0.2 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.2 |
rpoC | 764705 | p.Leu446Thr | missense_variant | 0.21 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.23 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.22 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.19 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.18 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.16 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472092 | n.247C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472120 | n.275G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472245 | n.400C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472506 | n.661A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472572 | n.727T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473047 | n.1202C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473093 | n.1248C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473094 | n.1249T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473111 | n.1266A>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473157 | n.1312C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473298 | n.1453A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473673 | n.16G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474139 | n.482C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474171 | n.514C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474287 | n.630T>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474290 | n.633T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474520 | n.863A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474717 | n.1060_1061insGGTTC | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474806 | n.1149A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474822 | n.1165G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474905 | n.1248T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475697 | n.2040C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475989 | n.2332T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475990 | n.2333G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476519 | n.2862C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.11 |
rpsA | 1834348 | c.807T>G | synonymous_variant | 0.16 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.14 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.14 |
rpsA | 1834361 | c.820_822delTTGinsCTC | synonymous_variant | 0.14 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.17 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.18 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.21 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.18 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
rpsA | 1834416 | p.Ala292Val | missense_variant | 0.19 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.18 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.2 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.17 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.12 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | 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 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.11 |
clpC1 | 4039790 | c.915C>A | synonymous_variant | 0.12 |
clpC1 | 4039829 | p.Leu292Phe | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |