Run ID: SRR1173719
Sample name:
Date: 03-04-2023 03:30:23
Number of reads: 232959
Percentage reads mapped: 6.8
Strain: lineage3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.06 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.51 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.53 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.96 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326284 | p.Leu397Arg | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5078 | c.-162_-161insG | upstream_gene_variant | 1.0 |
gyrB | 6248 | p.Leu337Ile | missense_variant | 0.25 |
gyrB | 6302 | p.Ala355Thr | missense_variant | 0.22 |
gyrA | 6307 | c.-995T>C | upstream_gene_variant | 0.3 |
gyrA | 6316 | c.-986G>C | upstream_gene_variant | 0.3 |
gyrB | 6323 | p.Val362Leu | missense_variant | 0.3 |
gyrA | 6326 | c.-976_-975delAGinsTC | upstream_gene_variant | 0.3 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.33 |
gyrA | 6362 | c.-940_-938delTTGinsCTC | upstream_gene_variant | 0.5 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620307 | c.417C>A | synonymous_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.67 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.75 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.75 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.75 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.5 |
rpoB | 761554 | p.Val583Ala | missense_variant | 0.5 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.4 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.4 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.4 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.4 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.4 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.4 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.4 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.33 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.33 |
rpoB | 761963 | c.2157G>C | synonymous_variant | 0.75 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.75 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.71 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.83 |
rpoB | 762015 | p.Glu737Ser | missense_variant | 0.83 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.78 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.6 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.6 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.6 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.6 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.44 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.4 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 0.4 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.4 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.33 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.33 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.43 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.43 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.43 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.43 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.5 |
rpoB | 762273 | p.Ala823Ser | missense_variant | 0.6 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.75 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.75 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.75 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.6 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.75 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.75 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.75 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.6 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.67 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.67 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.6 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.56 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.56 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.33 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.27 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.29 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.5 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.5 |
rpoB | 763077 | p.Val1091His | missense_variant | 0.5 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.5 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.4 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.4 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.44 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.5 |
rpoB | 763137 | p.Ile1111Val | missense_variant | 0.5 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.25 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.33 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.67 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.6 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.73 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.75 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.8 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.8 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.86 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.8 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.8 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.8 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.69 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.55 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.55 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.6 |
rpoC | 763639 | p.Glu90Asp | missense_variant | 0.64 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.67 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.75 |
rpoC | 763663 | c.294C>T | synonymous_variant | 0.77 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.82 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.9 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.86 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.86 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.86 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.67 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.67 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.67 |
rpoC | 764115 | p.Gly249Ala | missense_variant | 0.33 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.8 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.8 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.8 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.8 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.8 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.8 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.8 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.8 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.75 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.75 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.75 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.75 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.75 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.75 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.6 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.6 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.57 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.5 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.5 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.67 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.71 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.75 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.75 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.75 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.71 |
rpoC | 764572 | c.1203G>A | synonymous_variant | 0.71 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.71 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.75 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.78 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.88 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.67 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.8 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.89 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.89 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.89 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.75 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.78 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.78 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.67 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.67 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.6 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.6 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.67 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.5 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.5 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.5 |
rpoC | 767301 | p.Gly1311Val | missense_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776795 | c.1686C>T | synonymous_variant | 0.2 |
mmpL5 | 778006 | p.Glu159Lys | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472553 | n.708C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472584 | n.739A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472594 | n.749G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473391 | n.-267C>T | upstream_gene_variant | 0.6 |
rrl | 1473450 | n.-208C>T | upstream_gene_variant | 0.5 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473924 | n.267A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474186 | n.529A>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474711 | n.1054_1055insAA | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474944 | n.1287G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475488 | n.1831G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475491 | n.1834C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475540 | n.1883C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475551 | n.1894T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475564 | n.1907C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475574 | n.1917C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475575 | n.1918C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475576 | n.1919C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475990 | n.2333G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476630 | n.2973A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833653 | p.Ile38Leu | missense_variant | 0.33 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.33 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.43 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.6 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.62 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.62 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.62 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.5 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.56 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.56 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.57 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 0.5 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.4 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.4 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.33 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.33 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.33 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.29 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.5 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.57 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.8 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.8 |
rpsA | 1834398 | p.His286Leu | missense_variant | 0.8 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.86 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.86 |
rpsA | 1834418 | p.Ile293Leu | missense_variant | 0.86 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.88 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.89 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.89 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.89 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.89 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 1.0 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.71 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.71 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.57 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102621 | p.Ile141Asn | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156122 | c.-11G>C | upstream_gene_variant | 0.33 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.67 |
ahpC | 2725949 | c.-244G>A | upstream_gene_variant | 0.5 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2986922 | c.84C>A | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087176 | c.357C>T | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568787 | c.-108T>A | upstream_gene_variant | 0.22 |
rpoA | 3877848 | c.660C>A | synonymous_variant | 0.33 |
rpoA | 3877935 | p.Lys191Arg | missense_variant | 0.33 |
rpoA | 3877959 | c.549C>G | synonymous_variant | 0.33 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.29 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.25 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.25 |
rpoA | 3877981 | p.Tyr176Phe | missense_variant | 0.25 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.22 |
rpoA | 3877995 | c.513G>C | synonymous_variant | 0.22 |
rpoA | 3878001 | c.507A>C | synonymous_variant | 0.25 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.33 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.5 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.5 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.5 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.5 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.5 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.6 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.6 |
clpC1 | 4039865 | c.840T>G | synonymous_variant | 0.6 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.6 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.5 |
clpC1 | 4039974 | p.Asp244Gly | missense_variant | 0.36 |
clpC1 | 4039977 | p.Lys243Arg | missense_variant | 0.36 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.36 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.4 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.4 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.36 |
clpC1 | 4040003 | p.Val234Asp | missense_variant | 0.36 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.46 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.5 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.53 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.53 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.53 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.45 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.4 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.5 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.5 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.5 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248664 | c.2151G>T | synonymous_variant | 0.17 |
ubiA | 4269871 | c.-38G>T | upstream_gene_variant | 0.5 |
ethA | 4328154 | c.-681C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |