Run ID: SRR1062871
Sample name:
Date: 02-04-2023 18:37:49
Number of reads: 705185
Percentage reads mapped: 19.29
Strain: lineage4.3.4.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.98 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.98 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 0.94 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.33 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.7 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.72 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.51 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155128 | p.Trp328Cys | missense_variant | 0.13 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4326694 | c.440_779del | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5054 | c.-186G>C | upstream_gene_variant | 0.17 |
gyrB | 5739 | p.Thr167Met | missense_variant | 0.14 |
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 6346 | c.-956C>A | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8543 | c.1242C>T | synonymous_variant | 0.14 |
gyrA | 8780 | p.Asp493Glu | missense_variant | 0.33 |
gyrA | 9035 | c.1734G>A | synonymous_variant | 0.13 |
gyrA | 9061 | p.Ala587Val | missense_variant | 0.13 |
gyrA | 9083 | p.Gln594His | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491308 | p.Ala176Ser | missense_variant | 0.18 |
mshA | 576035 | p.Ala230Ser | missense_variant | 0.4 |
ccsA | 620008 | p.Arg40Ser | missense_variant | 0.2 |
ccsA | 620151 | c.261C>T | synonymous_variant | 0.5 |
ccsA | 620414 | p.His175Pro | missense_variant | 0.29 |
ccsA | 620464 | p.Ala192Ser | missense_variant | 0.29 |
rpoB | 759934 | p.Glu43Val | missense_variant | 0.22 |
rpoB | 760562 | p.Met252Ile | missense_variant | 0.29 |
rpoB | 760703 | c.897C>A | synonymous_variant | 0.14 |
rpoB | 761354 | c.1548C>A | synonymous_variant | 0.17 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.29 |
rpoB | 761559 | p.Thr585Ser | missense_variant | 0.29 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.31 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.29 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.26 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.25 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.28 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.29 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.28 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.22 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.21 |
rpoB | 761961 | p.Pro719Ser | missense_variant | 0.24 |
rpoB | 761973 | p.His723Tyr | missense_variant | 0.2 |
rpoB | 761980 | p.Tyr725Phe | missense_variant | 0.23 |
rpoB | 761987 | c.2181C>T | synonymous_variant | 0.24 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.23 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.25 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.26 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.33 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.35 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.35 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.38 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.41 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.4 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.31 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.33 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.31 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.27 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.2 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.23 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.33 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.41 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.33 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.33 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.33 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.32 |
rpoB | 762273 | p.Ala823Ser | missense_variant | 0.33 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.3 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.3 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.13 |
rpoC | 762866 | c.-504C>A | upstream_gene_variant | 0.18 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.24 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.24 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.38 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.23 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.58 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.63 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.3 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.61 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.3 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.31 |
rpoB | 762934 | c.3129_3130insAGCC | frameshift_variant | 0.3 |
rpoB | 762938 | c.3133_3136delATGA | frameshift_variant | 0.35 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.42 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.45 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.68 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.58 |
rpoB | 763002 | c.3197dupA | frameshift_variant | 0.33 |
rpoB | 763006 | c.3201delC | frameshift_variant | 0.25 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.23 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.23 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.25 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.23 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.25 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.14 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.27 |
rpoC | 763100 | c.-270G>A | upstream_gene_variant | 0.4 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.4 |
rpoB | 763122 | p.Ile1106Leu | missense_variant | 0.36 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.36 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.36 |
rpoC | 763136 | c.-234C>A | upstream_gene_variant | 0.36 |
rpoC | 763157 | c.-213G>C | upstream_gene_variant | 0.18 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.17 |
rpoB | 763161 | p.Leu1119Ile | missense_variant | 0.17 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.15 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.14 |
rpoB | 763170 | p.Leu1122Met | missense_variant | 0.14 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.22 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.27 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.42 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.43 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.56 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.57 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.55 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.54 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.53 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.51 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.5 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.5 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.57 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.61 |
rpoC | 763621 | c.252C>T | synonymous_variant | 0.57 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.59 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.59 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.57 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.59 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.6 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.64 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.62 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.62 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.56 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.56 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.56 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.56 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.56 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.56 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.42 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.33 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.17 |
rpoC | 764333 | p.Pro322Thr | missense_variant | 0.29 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.2 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.25 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.25 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.25 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.33 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.44 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.44 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.43 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.39 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.4 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.43 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.45 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.4 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.48 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.32 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.49 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.5 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.21 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.24 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.39 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.59 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.75 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.57 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.81 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.26 |
rpoC | 764663 | p.Val432Thr | missense_variant | 0.52 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.27 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.52 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.48 |
rpoC | 764679 | p.Lys437Ser | missense_variant | 0.26 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.2 |
rpoC | 764690 | p.Cys441Ala | missense_variant | 0.24 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.44 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.62 |
rpoC | 764705 | p.Leu446Thr | missense_variant | 0.56 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.61 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.56 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.41 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.36 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.38 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.42 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.33 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.43 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.31 |
rpoC | 764808 | p.Arg480His | missense_variant | 0.33 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.22 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.12 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.18 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.17 |
rpoC | 764957 | p.Glu530Ser | missense_variant | 0.18 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.82 |
rpoC | 764998 | c.1629G>C | synonymous_variant | 0.19 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.16 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.17 |
rpoC | 765014 | p.Ala549Pro | missense_variant | 0.17 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.18 |
rpoC | 765150 | p.Gly594Ala | missense_variant | 0.14 |
rpoC | 765958 | c.2589C>G | synonymous_variant | 0.13 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.13 |
rpoC | 766446 | p.Gly1026Val | missense_variant | 0.22 |
rpoC | 767064 | p.Val1232Ala | missense_variant | 0.67 |
rpoC | 767083 | c.3714C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775712 | c.2769G>T | synonymous_variant | 0.18 |
mmpL5 | 776257 | p.Ala742Thr | missense_variant | 0.13 |
mmpL5 | 776806 | p.Gly559Arg | missense_variant | 0.13 |
mmpR5 | 778007 | c.-983G>C | upstream_gene_variant | 0.13 |
mmpL5 | 779124 | c.-644C>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781417 | c.-143G>T | upstream_gene_variant | 0.18 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.17 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.2 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.33 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.33 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.29 |
rpsL | 781820 | c.261G>C | synonymous_variant | 0.31 |
rpsL | 781829 | c.270G>T | synonymous_variant | 0.36 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.33 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.29 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.21 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.25 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.2 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.2 |
rplC | 801080 | p.Ala91Asp | missense_variant | 0.22 |
fbiC | 1302959 | c.31_32delGC | frameshift_variant | 0.2 |
fbiC | 1304388 | c.1458C>T | synonymous_variant | 0.25 |
fbiC | 1305284 | p.Gln785Arg | missense_variant | 0.18 |
Rv1258c | 1406864 | c.477C>T | synonymous_variant | 0.2 |
Rv1258c | 1407279 | p.Ala21Glu | missense_variant | 0.22 |
Rv1258c | 1407534 | c.-194C>T | upstream_gene_variant | 0.14 |
embR | 1416725 | p.Trp208* | stop_gained | 0.25 |
embR | 1417240 | c.108G>A | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472092 | n.247C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472120 | n.275G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472245 | n.400C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472380 | n.535G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472415 | n.570T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472506 | n.661A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472572 | n.727T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472753 | n.908A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472826 | n.981G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473047 | n.1202C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473157 | n.1312C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473298 | n.1453A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473789 | n.133dupC | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473884 | n.227C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473898 | n.241C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474171 | n.514C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474287 | n.630T>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474290 | n.633T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474520 | n.863A>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474717 | n.1060_1061insGGTTC | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474806 | n.1149A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474822 | n.1165G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474905 | n.1248T>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474975 | n.1318G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475109 | n.1452C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475176 | n.1519G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475187 | n.1530C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475488 | n.1831G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475500 | n.1843_1844insT | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475536 | n.1879C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475697 | n.2040C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475989 | n.2332T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475990 | n.2333G>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476519 | n.2862C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476670 | n.3013A>G | non_coding_transcript_exon_variant | 0.19 |
fabG1 | 1673231 | c.-209G>T | upstream_gene_variant | 0.12 |
fabG1 | 1673246 | c.-194G>T | upstream_gene_variant | 0.12 |
fabG1 | 1673741 | p.Thr101Ser | missense_variant | 0.17 |
inhA | 1674491 | p.Phe97Tyr | missense_variant | 0.25 |
rpsA | 1833487 | c.-55C>G | upstream_gene_variant | 0.4 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.31 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.29 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.33 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.33 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.33 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.33 |
rpsA | 1833698 | p.Leu53Val | missense_variant | 0.31 |
rpsA | 1833709 | c.168C>A | synonymous_variant | 0.29 |
rpsA | 1833718 | c.177C>G | synonymous_variant | 0.29 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.2 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.23 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.23 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.17 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.15 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.18 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.25 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.31 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.33 |
rpsA | 1834416 | p.Ala292Val | missense_variant | 0.36 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.47 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.48 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.5 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.52 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.48 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.47 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.42 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.39 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.33 |
rpsA | 1834524 | p.Glu328Val | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918637 | p.Pro233Gln | missense_variant | 0.14 |
ndh | 2101740 | p.Gln435* | stop_gained | 0.13 |
ndh | 2102028 | p.Gly339Arg | missense_variant | 0.12 |
ndh | 2102294 | p.Thr250Ile | missense_variant | 0.17 |
katG | 2153948 | p.Gln722Glu | missense_variant | 0.17 |
katG | 2155605 | c.507C>A | synonymous_variant | 0.13 |
katG | 2156146 | c.-35A>T | upstream_gene_variant | 0.18 |
PPE35 | 2170342 | p.Gln91Lys | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289003 | p.Asp80Gly | missense_variant | 0.13 |
pncA | 2290095 | c.-854C>A | upstream_gene_variant | 0.2 |
eis | 2714700 | c.633C>T | synonymous_variant | 0.22 |
folC | 2746192 | c.1407C>A | synonymous_variant | 0.2 |
folC | 2746213 | c.1386G>A | synonymous_variant | 0.18 |
folC | 2746561 | c.1038C>G | synonymous_variant | 0.13 |
folC | 2746903 | c.696G>A | synonymous_variant | 0.15 |
pepQ | 2860148 | p.Gly91Ser | missense_variant | 0.22 |
pepQ | 2860466 | c.-48C>T | upstream_gene_variant | 0.13 |
ribD | 2987422 | p.Gly195Glu | missense_variant | 0.14 |
ribD | 2987487 | p.Pro217Ala | missense_variant | 0.25 |
Rv2752c | 3066124 | p.Gly23Ala | missense_variant | 0.17 |
thyX | 3067676 | c.270C>A | synonymous_variant | 0.29 |
thyA | 3073766 | p.Asp236Asn | missense_variant | 0.13 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086929 | p.Ala37Glu | missense_variant | 0.17 |
fbiD | 3339018 | c.-100G>C | upstream_gene_variant | 0.22 |
fbiD | 3339033 | c.-85G>T | upstream_gene_variant | 0.18 |
fbiD | 3339318 | c.201C>A | synonymous_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Leu | missense_variant | 0.13 |
fprA | 3474833 | p.Ile276Thr | missense_variant | 0.29 |
fprA | 3475339 | p.Ala445Ser | missense_variant | 0.25 |
whiB7 | 3568655 | p.Gln9Lys | missense_variant | 0.2 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3612448 | c.669G>A | synonymous_variant | 0.25 |
Rv3236c | 3612652 | c.465G>A | synonymous_variant | 0.22 |
Rv3236c | 3612807 | p.Gly104Ser | missense_variant | 0.2 |
fbiA | 3640594 | p.Gly18Arg | missense_variant | 0.18 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
alr | 3840869 | c.552C>G | synonymous_variant | 1.0 |
rpoA | 3878188 | c.319delG | frameshift_variant | 0.22 |
ddn | 3987197 | p.Glu118Asp | missense_variant | 0.14 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038443 | c.2262G>T | synonymous_variant | 0.2 |
clpC1 | 4039588 | p.Ser373Thr | missense_variant | 0.33 |
clpC1 | 4039593 | p.Arg371Lys | missense_variant | 0.29 |
clpC1 | 4039611 | p.Arg365Lys | missense_variant | 0.2 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.2 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.14 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.13 |
clpC1 | 4039667 | p.Gln346Phe | missense_variant | 0.13 |
clpC1 | 4039673 | c.1032G>T | synonymous_variant | 0.15 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.12 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 0.12 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.17 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.17 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 0.17 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.26 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.17 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.17 |
clpC1 | 4039754 | c.951G>C | synonymous_variant | 0.17 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.18 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.19 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.18 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.18 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.18 |
clpC1 | 4039790 | c.915C>A | synonymous_variant | 0.16 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.13 |
clpC1 | 4039976 | p.Lys243Thr | missense_variant | 0.38 |
clpC1 | 4039982 | p.Thr241Ile | missense_variant | 0.35 |
clpC1 | 4039991 | c.714G>T | synonymous_variant | 0.35 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.3 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.3 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.36 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.48 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.45 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.45 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.46 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.36 |
clpC1 | 4040066 | c.639G>T | synonymous_variant | 0.36 |
clpC1 | 4040081 | c.624C>G | synonymous_variant | 0.29 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.27 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.27 |
clpC1 | 4040096 | p.Val203Ile | missense_variant | 0.15 |
clpC1 | 4040274 | p.Gly144Val | missense_variant | 0.29 |
panD | 4044047 | p.Val79Leu | missense_variant | 0.17 |
embC | 4240895 | p.Arg345Gly | missense_variant | 0.18 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243033 | p.Trp1057Cys | missense_variant | 0.33 |
embA | 4243424 | c.192C>T | synonymous_variant | 0.18 |
embA | 4243482 | c.252delC | frameshift_variant | 0.13 |
embA | 4244523 | p.Pro431Ser | missense_variant | 0.17 |
embA | 4245205 | p.Gly658Glu | missense_variant | 0.15 |
embA | 4245454 | p.Ala741Asp | missense_variant | 0.12 |
embB | 4246686 | p.Trp58Leu | missense_variant | 0.25 |
embB | 4247455 | c.942C>A | synonymous_variant | 0.12 |
embB | 4247971 | c.1458C>A | synonymous_variant | 0.2 |
embB | 4248184 | p.Met557Ile | missense_variant | 0.22 |
embB | 4248519 | p.Ser669Ile | missense_variant | 0.18 |
embB | 4249312 | c.2799C>A | synonymous_variant | 0.15 |
embB | 4249472 | p.Asp987Tyr | missense_variant | 0.17 |
embB | 4249662 | p.Ala1050Val | missense_variant | 0.2 |
ethA | 4327436 | p.Gly13Val | missense_variant | 0.14 |
ethA | 4327536 | c.-63C>G | upstream_gene_variant | 0.17 |
ethR | 4327610 | p.Ser21Cys | missense_variant | 0.33 |
whiB6 | 4338288 | c.234G>T | synonymous_variant | 0.15 |
whiB6 | 4338459 | p.Met21Ile | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407604 | p.Ala200Val | missense_variant | 0.15 |
gid | 4407775 | p.Asp143Val | missense_variant | 0.17 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408212 | c.-10G>A | upstream_gene_variant | 0.15 |