Run ID: SRR14334194
Sample name:
Date: 03-04-2023 10:34:04
Number of reads: 2671659
Percentage reads mapped: 41.82
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7572 | p.Ser91Pro | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.46 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.3 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.27 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2154987 | c.1124dupC | frameshift_variant | 0.15 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289207 | p.Asp12Gly | missense_variant | 0.97 | pyrazinamide |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5509 | c.270C>A | synonymous_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8576 | c.1275C>A | synonymous_variant | 0.2 |
gyrA | 8840 | c.1539C>G | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575213 | c.-135G>C | upstream_gene_variant | 0.15 |
mshA | 575494 | c.147G>T | synonymous_variant | 0.25 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.4 |
rpoB | 760436 | c.630C>G | synonymous_variant | 0.4 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.4 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.4 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.4 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.25 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.14 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.17 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.17 |
rpoB | 760960 | p.Val385Ala | missense_variant | 0.12 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.2 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.2 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.14 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.14 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.18 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.12 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.25 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.2 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.2 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.2 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.12 |
rpoB | 762185 | c.2379_2380insC | frameshift_variant | 0.12 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.12 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.24 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.27 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.15 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.15 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.18 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.18 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.15 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.22 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.14 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.13 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.95 |
rpoB | 763083 | p.Arg1093Ser | missense_variant | 0.23 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.24 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.24 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.14 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.18 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.12 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.24 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.22 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.29 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.14 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.23 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.27 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.18 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.22 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.19 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.13 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.14 |
rpoC | 763926 | p.Ala186Val | missense_variant | 0.22 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.18 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.14 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.15 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.17 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.12 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.2 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.21 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.21 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.21 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.35 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.2 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.32 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.29 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.16 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.21 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.21 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.38 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.29 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.16 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.23 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.19 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.23 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.14 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.26 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.21 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.13 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.23 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.19 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.15 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.15 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 0.91 |
rpoC | 765350 | p.Ala661Ser | missense_variant | 0.29 |
rpoC | 766218 | p.Asp950Gly | missense_variant | 0.13 |
rpoC | 766636 | p.Phe1089Leu | missense_variant | 0.25 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.27 |
rpoC | 766690 | c.3321G>T | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777103 | p.Ala460Ser | missense_variant | 0.17 |
mmpL5 | 777851 | c.630C>A | synonymous_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304359 | c.1429_1431delCGCinsAGA | synonymous_variant | 0.25 |
fbiC | 1304908 | p.Gly660Trp | missense_variant | 0.21 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416968 | p.Ala127Asp | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472974 | n.1129A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1133dupT | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473099 | n.1254T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473132 | n.1287T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473135 | n.1290C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474903 | n.1246T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474918 | n.1261T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475063 | n.1406A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475076 | n.1419C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475110 | n.1454_1457delGGCC | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475118 | n.1461C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475120 | n.1463_1464insTCTC | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475129 | n.1472G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475137 | n.1480A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475170 | n.1513A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475190 | n.1533T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475197 | n.1540G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475224 | n.1567T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475552 | n.1895G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475756 | n.2101_2108delACCCGCAA | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.42 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.12 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.13 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.17 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.12 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.12 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.12 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.12 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.14 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101990 | c.1053G>T | synonymous_variant | 0.14 |
ndh | 2102392 | c.651C>A | synonymous_variant | 0.15 |
ndh | 2102398 | c.645C>T | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155051 | p.Thr354Ile | missense_variant | 0.18 |
katG | 2155389 | c.723C>A | synonymous_variant | 0.18 |
katG | 2155784 | p.Ala110Ser | missense_variant | 0.22 |
katG | 2155787 | p.Ala109Thr | missense_variant | 0.22 |
katG | 2155794 | c.318G>A | synonymous_variant | 0.22 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.33 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.14 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168255 | c.2357delT | frameshift_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.18 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.17 |
PPE35 | 2170351 | p.Thr88Ala | missense_variant | 0.13 |
PPE35 | 2170372 | p.Thr81Ala | missense_variant | 0.18 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.15 |
PPE35 | 2170547 | c.66A>C | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714131 | p.Glu401Gly | missense_variant | 0.15 |
eis | 2714136 | c.1197G>T | synonymous_variant | 0.15 |
eis | 2715005 | p.Asp110Tyr | missense_variant | 0.15 |
eis | 2715579 | c.-247G>C | upstream_gene_variant | 0.33 |
folC | 2746789 | p.Ile270Met | missense_variant | 0.14 |
pepQ | 2859877 | p.Leu181Pro | missense_variant | 0.17 |
thyX | 3068083 | c.-138T>C | upstream_gene_variant | 0.12 |
thyX | 3068091 | c.-146T>G | upstream_gene_variant | 0.12 |
thyA | 3074532 | c.-61C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339650 | p.Leu178Pro | missense_variant | 0.14 |
Rv3083 | 3449209 | p.Asp236Tyr | missense_variant | 0.22 |
Rv3083 | 3449753 | p.Gly417Val | missense_variant | 0.16 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474035 | p.Gly10Val | missense_variant | 0.17 |
fprA | 3474099 | p.Asp31Glu | missense_variant | 0.22 |
fprA | 3474243 | c.237C>T | synonymous_variant | 0.15 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878624 | c.-117C>A | upstream_gene_variant | 0.33 |
ddn | 3986653 | c.-191G>C | upstream_gene_variant | 0.14 |
clpC1 | 4038173 | p.Glu844Asp | missense_variant | 0.18 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.12 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.12 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.15 |
clpC1 | 4039838 | c.867G>C | synonymous_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.14 |
clpC1 | 4039929 | p.Ser259Thr | missense_variant | 0.13 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.13 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.14 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.14 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.21 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.12 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.16 |
embC | 4240982 | p.Ser374Gly | missense_variant | 0.12 |
embC | 4242096 | p.Ala745Asp | missense_variant | 0.2 |
embC | 4242377 | p.Leu839Met | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242735 | p.Ile958Thr | missense_variant | 0.12 |
embA | 4243115 | c.-118C>T | upstream_gene_variant | 0.14 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244845 | c.1614dupC | frameshift_variant | 0.17 |
embA | 4245739 | p.Arg836His | missense_variant | 0.33 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.36 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.21 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.27 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.27 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.31 |
embB | 4246712 | p.Val67Leu | missense_variant | 0.15 |
embB | 4246897 | c.384C>A | synonymous_variant | 0.2 |
embB | 4247739 | p.Ala409Glu | missense_variant | 0.15 |
embB | 4249757 | p.Thr1082Ala | missense_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268623 | p.Trp72Arg | missense_variant | 0.5 |
aftB | 4268848 | c.-12C>A | upstream_gene_variant | 0.15 |
ubiA | 4269116 | p.Arg240Cys | missense_variant | 1.0 |
ethA | 4326125 | p.Gly450Val | missense_variant | 0.18 |
ethA | 4326405 | p.Asp357Tyr | missense_variant | 1.0 |
ethA | 4327275 | p.Arg67Ser | missense_variant | 0.22 |
ethR | 4328055 | p.His169Gln | missense_variant | 0.13 |
ethA | 4328458 | c.-985C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407605 | p.Ala200Thr | missense_variant | 0.13 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408414 | c.-212G>T | upstream_gene_variant | 0.18 |