Run ID: ERR2229234
Sample name:
Date: 31-03-2023 16:51:12
Number of reads: 1379208
Percentage reads mapped: 89.04
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 | 761127 | p.Ser441Ala | missense_variant | 0.12 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.15 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7608 | p.Trp103Arg | missense_variant | 0.14 |
gyrA | 7777 | p.Arg159Gln | missense_variant | 0.13 |
gyrA | 8011 | p.Ser237Phe | missense_variant | 0.11 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.25 |
mshA | 576741 | p.Ala465Glu | missense_variant | 0.14 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.12 |
rpoB | 761133 | p.Leu443Met | missense_variant | 0.12 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.14 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.18 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.17 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.12 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.13 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.14 |
rpoB | 761193 | p.Gly463Ser | missense_variant | 0.15 |
rpoB | 762024 | p.Val740Leu | missense_variant | 0.13 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.12 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.25 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.24 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.16 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.17 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.29 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.19 |
rpoB | 762180 | p.Asp792Ser | missense_variant | 0.19 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.16 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.21 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.19 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.1 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.13 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.29 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.29 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.12 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.12 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.12 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.11 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.13 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.24 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.28 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.31 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.31 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.29 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.33 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.29 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.35 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.35 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.41 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.36 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.37 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.35 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.38 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.31 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.34 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.29 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.25 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.23 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.17 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.17 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.15 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.11 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.11 |
rpoC | 765324 | p.Gly652Val | missense_variant | 0.18 |
rpoC | 765691 | c.2322G>T | synonymous_variant | 0.17 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.12 |
rpoC | 765923 | p.Asn852Ala | missense_variant | 0.14 |
rpoC | 765940 | c.2571A>C | synonymous_variant | 0.14 |
rpoC | 765947 | c.2578_2580delTTGinsCTC | synonymous_variant | 0.13 |
rpoC | 765962 | c.2593_2595delTTGinsCTC | synonymous_variant | 0.18 |
rpoC | 765970 | c.2601C>G | synonymous_variant | 0.19 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.19 |
rpoC | 766000 | c.2631G>C | synonymous_variant | 0.12 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.11 |
rpoC | 766366 | c.2997C>A | synonymous_variant | 0.14 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.22 |
rpoC | 767008 | c.3639G>C | synonymous_variant | 0.22 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777199 | p.Asn428His | missense_variant | 0.12 |
mmpL5 | 778126 | p.Asp119Tyr | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406286 | p.Met352Thr | missense_variant | 0.12 |
embR | 1416785 | p.Ser188Ile | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472712 | n.867G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473284 | n.1439A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473841 | n.184A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473969 | n.312G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474006 | n.349G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474627 | n.970G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474683 | n.1026C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474717 | n.1060A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474722 | n.1065T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474758 | n.1101G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475759 | n.2102C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476295 | n.2638C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.33 |
inhA | 1674397 | p.Gln66Lys | missense_variant | 0.25 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.16 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.16 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.16 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.17 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.17 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.25 |
rpsA | 1833776 | p.Val79Ile | missense_variant | 0.12 |
rpsA | 1833992 | p.Ser151Thr | missense_variant | 0.14 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.13 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102403 | p.Leu214Ile | missense_variant | 0.12 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.14 |
katG | 2154041 | p.Gly691Ser | missense_variant | 0.12 |
katG | 2154084 | c.2028G>T | synonymous_variant | 0.12 |
katG | 2155380 | c.732G>T | synonymous_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.14 |
PPE35 | 2169884 | c.729T>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.45 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.14 |
PPE35 | 2170372 | p.Thr81Ala | missense_variant | 0.14 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.11 |
PPE35 | 2170566 | p.Phe16Tyr | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289189 | p.Ser18Leu | missense_variant | 0.11 |
kasA | 2518363 | c.249C>A | synonymous_variant | 0.15 |
kasA | 2518391 | p.Gln93Lys | missense_variant | 0.14 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.29 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.24 |
kasA | 2519066 | p.Gly318Cys | missense_variant | 0.14 |
eis | 2715055 | p.Arg93Leu | missense_variant | 0.12 |
ahpC | 2726638 | p.Ala149Asp | missense_variant | 0.14 |
folC | 2746164 | p.Arg479Trp | missense_variant | 0.12 |
folC | 2746843 | c.756C>T | synonymous_variant | 0.29 |
folC | 2747213 | p.Pro129Leu | missense_variant | 0.13 |
folC | 2747512 | p.Gln29His | missense_variant | 0.15 |
folC | 2747659 | c.-61A>C | upstream_gene_variant | 0.17 |
thyA | 3074580 | c.-109T>C | upstream_gene_variant | 0.12 |
Rv3236c | 3612804 | c.312delT | frameshift_variant | 0.17 |
Rv3236c | 3612877 | c.240C>G | synonymous_variant | 0.2 |
fbiA | 3641309 | p.Ala256Gly | missense_variant | 0.11 |
fbiB | 3642241 | p.Gly236Val | missense_variant | 0.14 |
fbiB | 3642493 | p.Asp320Gly | missense_variant | 0.15 |
alr | 3841025 | c.396G>T | synonymous_variant | 0.11 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.4 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.13 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.17 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.12 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.23 |
embC | 4241221 | c.1359C>A | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244303 | p.Asn357Lys | missense_variant | 0.14 |
embB | 4245824 | c.-690G>A | upstream_gene_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.42 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.23 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.3 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.3 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.22 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.2 |
aftB | 4268840 | c.-4G>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |