Run ID: SRR22175249
Sample name:
Date: 04-04-2023 04:02:54
Number of reads: 1015419
Percentage reads mapped: 45.11
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 | 7582 | p.Asp94Gly | missense_variant | 0.97 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.94 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.95 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.63 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.66 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.53 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288766 | p.Leu159Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326922 | c.549_551delTGG | disruptive_inframe_deletion | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491290 | p.Val170Met | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.14 |
rpoB | 760920 | p.Leu372Met | missense_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.14 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.18 |
rpoB | 760944 | p.Gln380Glu | missense_variant | 0.14 |
rpoB | 760955 | c.1151_1152insCACG | frameshift_variant | 0.2 |
rpoB | 760961 | c.1156_1159delGGCA | frameshift_variant | 0.24 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.37 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.36 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.42 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.48 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.5 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.12 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.62 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.13 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.71 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.9 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.9 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.7 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.8 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.7 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.18 |
rpoB | 761084 | c.1278C>G | synonymous_variant | 0.42 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.42 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.44 |
rpoB | 761941 | c.2137delC | frameshift_variant | 0.15 |
rpoB | 761973 | p.His723Tyr | missense_variant | 0.12 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.11 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.12 |
rpoB | 762009 | p.Leu735Ile | missense_variant | 0.12 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.11 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.11 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.11 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.14 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.18 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.28 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.28 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.28 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.26 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.27 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.33 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.31 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.34 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.31 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.26 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.25 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.36 |
rpoB | 762152 | c.2346C>G | synonymous_variant | 0.26 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.35 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.28 |
rpoB | 762176 | c.2370T>G | synonymous_variant | 0.36 |
rpoB | 762178 | p.Arg791Gln | missense_variant | 0.14 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.14 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.44 |
rpoB | 762189 | p.Ile795Leu | missense_variant | 0.3 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.45 |
rpoB | 762197 | c.2391C>G | synonymous_variant | 0.17 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.38 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.38 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.14 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.35 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.21 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.18 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.29 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.14 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.12 |
rpoB | 762273 | p.Ala823Ser | missense_variant | 0.12 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.17 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.14 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.13 |
rpoB | 762299 | c.2493G>C | synonymous_variant | 0.14 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.13 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.13 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.22 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.23 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.21 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.24 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.2 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.21 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.16 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.13 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.12 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.12 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.13 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.14 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.11 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.2 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.23 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.24 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.25 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.13 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.18 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.13 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.19 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.24 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.33 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.32 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.38 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.33 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.27 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.22 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.21 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.21 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.24 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.19 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.13 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.11 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.11 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.11 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.17 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.13 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.16 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.16 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.17 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.17 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.15 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.14 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.15 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.15 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.11 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.26 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.24 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.29 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.23 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.3 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.31 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.3 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.26 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.13 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.26 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.46 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.47 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.22 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.54 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.22 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.52 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.2 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.21 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.54 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.21 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.53 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.21 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.21 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.33 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.23 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.39 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 0.3 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.23 |
rpoC | 764703 | p.Lys445Arg | missense_variant | 0.45 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.52 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.29 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.24 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.27 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.3 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.11 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.47 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.46 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.34 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.12 |
rpoC | 764759 | p.Asn464Asp | missense_variant | 0.31 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.41 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.35 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.18 |
rpoC | 764801 | c.1433_1434insTG | frameshift_variant | 0.12 |
rpoC | 764804 | c.1436_1437delAG | frameshift_variant | 0.13 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.24 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.24 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.25 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.17 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.29 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.2 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.15 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.17 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.15 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.12 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.12 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.12 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.12 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.12 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.12 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.12 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.13 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.12 |
rpoC | 764941 | c.1572G>C | synonymous_variant | 0.11 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.11 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.1 |
rpoC | 764958 | p.Glu530Gly | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775966 | p.Ala839Thr | missense_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473091 | n.1246G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473109 | n.1264T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473120 | n.1275C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473957 | n.300G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474292 | n.636_649delTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474355 | n.698A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474715 | n.1061delA | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475756 | n.2101dupA | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475765 | n.2108A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475768 | n.2112dupT | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476519 | n.2862C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.15 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.17 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.19 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.14 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.17 |
rpsA | 1833782 | p.Ser81Gly | missense_variant | 0.2 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.16 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.19 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.14 |
rpsA | 1833815 | p.Thr92His | missense_variant | 0.11 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.23 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.23 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.33 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 0.14 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.18 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.3 |
rpsA | 1833896 | p.Leu119Val | missense_variant | 0.3 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.29 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.3 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.3 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.34 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.32 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.38 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.42 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.23 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.36 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.16 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.34 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.13 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.24 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.32 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.11 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.16 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.19 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.17 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.2 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.16 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.25 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.16 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.17 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.11 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.14 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.15 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.15 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.15 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.33 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.4 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.4 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.39 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.38 |
rpsA | 1834310 | p.Glu257Lys | missense_variant | 0.25 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.32 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.13 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.14 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.37 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.3 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.22 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.19 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.29 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.29 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.19 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.19 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.26 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.28 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.23 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.23 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.22 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.19 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.17 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.12 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.12 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154069 | c.2043G>A | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642549 | p.Gln339Lys | missense_variant | 0.13 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.12 |
clpC1 | 4038881 | c.1824C>T | synonymous_variant | 0.12 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.15 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.19 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.18 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.19 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.18 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.17 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.15 |
clpC1 | 4039997 | c.708C>G | synonymous_variant | 0.16 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.15 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.18 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.16 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.18 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.26 |
clpC1 | 4040027 | c.678C>G | synonymous_variant | 0.16 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.13 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.11 |
embC | 4241022 | p.Ala387Val | missense_variant | 0.96 |
embC | 4241443 | c.1581C>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243190 | c.-43G>C | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408382 | c.-180A>G | upstream_gene_variant | 0.11 |