Run ID: ERR2027290
Sample name:
Date: 31-03-2023 15:42:15
Number of reads: 174072
Percentage reads mapped: 11.9
Strain: lineage3.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.13 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.71 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.71 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.24 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.55 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.46 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.39 | kanamycin, capreomycin, aminoglycosides, amikacin |
embB | 4247193 | p.Val227Gly | missense_variant | 0.29 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7467 | p.Leu56Phe | missense_variant | 0.5 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8732 | c.1431G>T | synonymous_variant | 0.5 |
gyrA | 8957 | c.1656C>T | synonymous_variant | 1.0 |
gyrA | 8986 | p.Ser562Phe | missense_variant | 1.0 |
gyrA | 8989 | p.Thr563Ile | missense_variant | 1.0 |
gyrA | 9037 | p.Ala579Val | missense_variant | 1.0 |
gyrA | 9212 | c.1911G>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491592 | c.810G>A | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491750 | p.Leu323Pro | missense_variant | 0.4 |
ccsA | 620039 | p.Pro50Leu | missense_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.5 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.5 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.5 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.5 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.5 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.43 |
rpoB | 761088 | c.1282_1284delAGCinsTCT | synonymous_variant | 0.43 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.43 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.43 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.6 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.43 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.6 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.71 |
rpoB | 761138 | c.1332C>T | synonymous_variant | 0.29 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.29 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.6 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.29 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.6 |
rpoB | 761165 | c.1359G>T | synonymous_variant | 0.6 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.29 |
rpoB | 761175 | c.1369C>T | synonymous_variant | 0.29 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.67 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.71 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.43 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.6 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.71 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.71 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.71 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.71 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.57 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.71 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.62 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.57 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.29 |
rpoB | 761246 | c.1440C>T | synonymous_variant | 0.29 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.29 |
rpoB | 761250 | p.Thr482Ser | missense_variant | 0.29 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.8 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.4 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.4 |
rpoB | 761818 | p.Arg671Pro | missense_variant | 0.5 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.33 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.33 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.33 |
rpoB | 761998 | c.2193_2195delGTC | disruptive_inframe_deletion | 0.33 |
rpoB | 762004 | p.Asn733Ser | missense_variant | 0.33 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.25 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.45 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.45 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.45 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.45 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.45 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.33 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.45 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.45 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.56 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.22 |
rpoB | 762104 | c.2298C>T | synonymous_variant | 0.33 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.56 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.43 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.33 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.33 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.33 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.33 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.33 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.33 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.33 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.43 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.43 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.43 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.43 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.43 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.43 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.43 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.43 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.33 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.33 |
rpoC | 762446 | c.-924C>T | upstream_gene_variant | 1.0 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
rpoC | 762470 | c.-900G>T | upstream_gene_variant | 1.0 |
rpoB | 762471 | p.Ile889Val | missense_variant | 1.0 |
rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
rpoC | 762494 | c.-876G>A | upstream_gene_variant | 1.0 |
rpoC | 762509 | c.-861T>A | upstream_gene_variant | 1.0 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
rpoC | 762518 | c.-852C>T | upstream_gene_variant | 1.0 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.5 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.5 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.5 |
rpoB | 762871 | p.Met1022Thr | missense_variant | 0.5 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.25 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.75 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.25 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.33 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.33 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.33 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.33 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.33 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.33 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.5 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.27 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.36 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.27 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.27 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.42 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.45 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.18 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.56 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.43 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.33 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.29 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.29 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.3 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.5 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.5 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.5 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.22 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.45 |
rpoB | 763077 | p.Val1091Ser | missense_variant | 0.45 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.45 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.45 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.45 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.5 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.5 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.4 |
rpoC | 763480 | c.111C>T | synonymous_variant | 0.2 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.2 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.4 |
rpoC | 763492 | c.123G>A | synonymous_variant | 0.25 |
rpoC | 763496 | p.Lys43Arg | missense_variant | 0.2 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 0.23 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 0.23 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.38 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.38 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.38 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.38 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.38 |
rpoC | 763555 | c.186C>T | synonymous_variant | 0.23 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.57 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.57 |
rpoC | 763598 | p.Arg77Lys | missense_variant | 0.35 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.4 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.59 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.47 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.59 |
rpoC | 763625 | p.Lys86Arg | missense_variant | 0.35 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.35 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.47 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.27 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.67 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.21 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.45 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.61 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.45 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.5 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.22 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.56 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.62 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.62 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.62 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.38 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.62 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.62 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.71 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.71 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.71 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.35 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.53 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.25 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.67 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.62 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.82 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.82 |
rpoC | 764368 | c.999C>T | synonymous_variant | 0.31 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.6 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.6 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.6 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.6 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.69 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.69 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.69 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 0.69 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.69 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.69 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.69 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.69 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.69 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.69 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.38 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.69 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.69 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.71 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.78 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.78 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.79 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.75 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.33 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.75 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.78 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.33 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.69 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.73 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.64 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.75 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.5 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.86 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.86 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.44 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.57 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.71 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.67 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.6 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.6 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.6 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.6 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.6 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.5 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.6 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.4 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.5 |
rpoC | 765832 | c.2463G>A | synonymous_variant | 0.67 |
rpoC | 766110 | p.Pro914Leu | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800632 | c.-177_-176delATinsTC | upstream_gene_variant | 1.0 |
rplC | 800639 | c.-170C>G | upstream_gene_variant | 1.0 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.5 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.5 |
rplC | 800737 | c.-72T>A | upstream_gene_variant | 1.0 |
rplC | 800766 | c.-43G>T | upstream_gene_variant | 1.0 |
embR | 1416689 | p.Arg220Gln | missense_variant | 0.29 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472286 | n.441_442insT | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472292 | n.447A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472313 | n.469_470delAT | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472319 | n.474C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472330 | n.485G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472332 | n.487A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472460 | n.614_615insCCCG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472846 | n.1002delG | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472846 | n.1002G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472849 | n.1005delT | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472868 | n.1023T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472874 | n.1029C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472875 | n.1030_1031insTTAGTTGGTC | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.37 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474282 | n.625G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474437 | n.782_784delATA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474674 | n.1018delC | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475174 | n.1517C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475610 | n.1953G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475618 | n.1961_1962insA | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475623 | n.1966_1967insT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475631 | n.1975delC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476075 | n.2418_2419insGTCA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476078 | n.2422_2425delGTAT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476088 | n.2431A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476096 | n.2439T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476097 | n.2440C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476100 | n.2443A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476116 | n.2459A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.6 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.6 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.6 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.4 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.5 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.33 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.33 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.67 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.33 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.33 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.67 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.33 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.67 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.33 |
rpsA | 1833769 | c.228C>T | synonymous_variant | 0.5 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.5 |
rpsA | 1833776 | p.Val79Ile | missense_variant | 0.5 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.5 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.5 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.5 |
rpsA | 1833808 | c.267G>T | synonymous_variant | 0.5 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
rpsA | 1833958 | c.417C>T | synonymous_variant | 0.25 |
rpsA | 1833967 | c.426C>T | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 1.0 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 1.0 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.8 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.2 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
rpsA | 1834023 | c.482_483insC | frameshift_variant | 1.0 |
rpsA | 1834026 | c.486delG | frameshift_variant | 0.8 |
rpsA | 1834030 | c.489C>T | synonymous_variant | 0.8 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.2 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.8 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 1.0 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.8 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.2 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.8 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 1.0 |
rpsA | 1834063 | c.522C>T | synonymous_variant | 0.2 |
rpsA | 1834081 | c.540C>A | synonymous_variant | 0.5 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.5 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.5 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 1.0 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.92 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.31 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.85 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.87 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.8 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 1.0 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.21 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.86 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.83 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.8 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.7 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.78 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.8 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.78 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.8 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.8 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.8 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.86 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.86 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.86 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.86 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.83 |
rpsA | 1834526 | p.Arg329Ser | missense_variant | 0.5 |
ndh | 2102864 | p.Thr60Ile | missense_variant | 0.5 |
katG | 2154498 | c.1614G>A | synonymous_variant | 0.33 |
katG | 2154618 | c.1494C>T | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156395 | c.-284G>T | upstream_gene_variant | 0.5 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.67 |
PPE35 | 2169039 | p.Gly525Asp | missense_variant | 0.67 |
PPE35 | 2169977 | c.636C>A | synonymous_variant | 1.0 |
Rv1979c | 2222444 | p.Ala241Ser | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518222 | c.108G>T | synonymous_variant | 0.5 |
eis | 2715087 | c.246C>A | synonymous_variant | 0.4 |
eis | 2715228 | c.105C>T | synonymous_variant | 0.4 |
ahpC | 2725947 | c.-246C>A | upstream_gene_variant | 0.5 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726216 | p.Asp8Glu | missense_variant | 0.33 |
folC | 2746248 | p.Ala451Thr | missense_variant | 0.5 |
ribD | 2987166 | p.Gly110Ser | missense_variant | 0.33 |
Rv2752c | 3064533 | c.1659G>T | synonymous_variant | 0.5 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474404 | p.Asn133Ile | missense_variant | 0.67 |
fprA | 3474702 | c.696C>T | synonymous_variant | 1.0 |
fbiA | 3641515 | p.Asp325Asn | missense_variant | 0.29 |
fbiB | 3641849 | c.315C>T | synonymous_variant | 0.5 |
alr | 3840282 | p.Ala380Asp | missense_variant | 0.33 |
alr | 3840371 | c.1050G>A | synonymous_variant | 0.33 |
alr | 3841246 | p.Ala59Thr | missense_variant | 1.0 |
ddn | 3986822 | c.-22C>A | upstream_gene_variant | 0.29 |
clpC1 | 4038410 | c.2295C>T | synonymous_variant | 0.5 |
clpC1 | 4039669 | p.Gln346Lys | missense_variant | 0.2 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.33 |
clpC1 | 4039709 | c.996C>T | synonymous_variant | 0.17 |
clpC1 | 4039711 | p.Tyr331His | missense_variant | 0.21 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.38 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.25 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.31 |
clpC1 | 4039742 | c.963C>G | synonymous_variant | 0.17 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.36 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.43 |
clpC1 | 4039754 | c.951G>C | synonymous_variant | 0.29 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.29 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.43 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.29 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.43 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.43 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.43 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.36 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.43 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.42 |
clpC1 | 4039793 | c.912C>T | synonymous_variant | 0.18 |
clpC1 | 4039799 | p.Ile302Val | missense_variant | 0.25 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.25 |
clpC1 | 4039805 | c.900C>G | synonymous_variant | 0.25 |
clpC1 | 4039811 | c.894C>T | synonymous_variant | 0.18 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.33 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.25 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.71 |
clpC1 | 4039835 | c.870C>T | synonymous_variant | 0.25 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.57 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.83 |
clpC1 | 4039858 | p.Ile283Val | missense_variant | 0.22 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.44 |
clpC1 | 4039873 | p.Thr278Ser | missense_variant | 0.22 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.43 |
clpC1 | 4039877 | c.828C>T | synonymous_variant | 0.29 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 0.29 |
clpC1 | 4039889 | c.816G>T | synonymous_variant | 0.33 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.4 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.3 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.2 |
clpC1 | 4039981 | p.Leu242Ile | missense_variant | 0.18 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.33 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.33 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.25 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.25 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.22 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.33 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.33 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.43 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.33 |
clpC1 | 4040072 | c.633C>T | synonymous_variant | 0.33 |
panD | 4044337 | c.-56G>A | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245296 | c.2064G>A | synonymous_variant | 0.4 |
embB | 4246214 | c.-300C>A | upstream_gene_variant | 0.33 |
embB | 4247216 | p.Ala235Thr | missense_variant | 0.29 |
embB | 4247328 | p.Ser272Asn | missense_variant | 0.33 |
embB | 4248723 | p.Trp737Leu | missense_variant | 0.5 |
embB | 4248808 | c.2295G>A | synonymous_variant | 1.0 |
aftB | 4267690 | p.Ala383Ser | missense_variant | 1.0 |
aftB | 4268874 | c.-38T>C | upstream_gene_variant | 0.22 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |