Run ID: SRR5007161
Sample name:
Date: 04-04-2023 07:51:04
Number of reads: 222057
Percentage reads mapped: 9.34
Strain: lineage4.1.1.3.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
lineage4.1.1.3.1 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.62 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.42 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.48 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.21 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.22 | kanamycin, capreomycin, aminoglycosides, amikacin |
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 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.5 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.67 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.5 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.8 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.4 |
rpoB | 761031 | p.Gln409Asn | missense_variant | 0.4 |
rpoB | 761037 | c.1231_1233delTTGinsCTC | synonymous_variant | 0.83 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.4 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.83 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761058 | p.Val418Thr | missense_variant | 0.33 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.23 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.62 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.64 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.2 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.67 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.6 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.62 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.57 |
rpoB | 761154 | p.Ser450Asn | missense_variant | 0.33 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.53 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.62 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.5 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.56 |
rpoB | 761193 | p.Gly463Ser | missense_variant | 0.5 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.36 |
rpoB | 761217 | p.Pro471Thr | missense_variant | 0.33 |
rpoB | 761231 | c.1425C>G | synonymous_variant | 0.33 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.25 |
rpoB | 761521 | p.Tyr572Phe | missense_variant | 0.43 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.33 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.33 |
rpoB | 761557 | p.Ala584Gly | missense_variant | 0.27 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.25 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.3 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.3 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.4 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.3 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.31 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.31 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.21 |
rpoB | 761642 | c.1836G>C | synonymous_variant | 0.2 |
rpoB | 761643 | p.Val613Ile | missense_variant | 0.2 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.27 |
rpoB | 761649 | p.Ser615Pro | missense_variant | 0.2 |
rpoB | 761654 | p.Glu616Asp | missense_variant | 0.2 |
rpoB | 761672 | c.1866C>G | synonymous_variant | 0.14 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.21 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.25 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.29 |
rpoB | 761997 | p.Leu731Ile | missense_variant | 0.29 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.29 |
rpoB | 762009 | p.Leu735Val | missense_variant | 0.25 |
rpoB | 762016 | p.Glu737Ala | missense_variant | 0.22 |
rpoB | 762024 | p.Val740Met | missense_variant | 0.44 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.5 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.5 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.56 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.56 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.2 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.45 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.18 |
rpoB | 762085 | p.Ala760Asp | missense_variant | 0.45 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.42 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.15 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.58 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.58 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.6 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.6 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.55 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.5 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.43 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.57 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.62 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.5 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.58 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.5 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.55 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.58 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.7 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.36 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.18 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.3 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.5 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.5 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.18 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.27 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.14 |
rpoC | 762842 | c.-528G>C | upstream_gene_variant | 0.2 |
rpoC | 762854 | c.-516G>C | upstream_gene_variant | 0.27 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.62 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.65 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.65 |
rpoB | 762871 | p.Met1022Thr | missense_variant | 0.35 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.35 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.71 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.69 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.28 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.39 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.33 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.29 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.65 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.69 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.24 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.24 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.56 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.28 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.76 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.62 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.78 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.75 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.29 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.74 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.81 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.83 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.44 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.83 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.7 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.79 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.79 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.72 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.67 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.54 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.29 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.29 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.44 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.55 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.64 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.77 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.73 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.87 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.87 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.87 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.75 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.81 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.81 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.9 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.9 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.81 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.79 |
rpoC | 763606 | c.237C>A | synonymous_variant | 0.85 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.79 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.83 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.79 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.67 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.68 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.6 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.58 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.61 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.52 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.52 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.53 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.58 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.47 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.43 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.43 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.43 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.46 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.46 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.46 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.3 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.4 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.4 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.4 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.4 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.4 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.4 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.4 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.33 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.4 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.9 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.87 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.58 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.2 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.82 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.87 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.67 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.87 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.2 |
rpoC | 764527 | c.1158C>A | synonymous_variant | 0.2 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.33 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 0.25 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.83 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.2 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.62 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.73 |
rpoC | 764549 | p.Pro394Val | missense_variant | 0.17 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.18 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.41 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.22 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.54 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.54 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.72 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.72 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.52 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.56 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.17 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.17 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.57 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.18 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.17 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.39 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.55 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.17 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.25 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.58 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.17 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.38 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.38 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.24 |
rpoC | 764703 | p.Lys445Ser | missense_variant | 0.15 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.42 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.45 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.33 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.23 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.17 |
rpoC | 765988 | c.2619G>C | synonymous_variant | 0.2 |
rpoC | 765991 | c.2622C>G | synonymous_variant | 0.2 |
rpoC | 765994 | c.2625A>C | synonymous_variant | 0.2 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 0.18 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.25 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.3 |
rplC | 800632 | c.-177_-176delATinsTC | upstream_gene_variant | 0.3 |
rplC | 800639 | c.-170C>G | upstream_gene_variant | 0.3 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.3 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.3 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.27 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.3 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.3 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.38 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.38 |
rplC | 800715 | c.-94A>G | upstream_gene_variant | 0.38 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.38 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.38 |
rplC | 800729 | c.-80G>C | upstream_gene_variant | 0.43 |
rplC | 800733 | c.-76A>G | upstream_gene_variant | 0.43 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.43 |
rplC | 800742 | c.-67G>T | upstream_gene_variant | 0.43 |
rplC | 800753 | c.-56C>T | upstream_gene_variant | 0.43 |
rplC | 800754 | c.-55A>C | upstream_gene_variant | 0.43 |
fbiC | 1303601 | p.Glu224Gly | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472290 | n.445C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472295 | n.450A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472297 | n.453_454insCCTG | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472686 | n.843dupT | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473284 | n.1439A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.17 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474309 | n.653delT | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474309 | n.653T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474315 | n.658A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474945 | n.1288C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833641 | p.Asn34Asp | missense_variant | 0.41 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.47 |
rpsA | 1833652 | c.111C>T | synonymous_variant | 0.5 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.73 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.67 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.67 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.67 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.62 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.54 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.67 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.58 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.6 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.61 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.61 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.14 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.6 |
rpsA | 1833776 | p.Val79Ile | missense_variant | 0.5 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.36 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.33 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.3 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.33 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.33 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.33 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.33 |
rpsA | 1833926 | p.Thr129Ser | missense_variant | 0.3 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.62 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.38 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.38 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.39 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.68 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.19 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.7 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.69 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.3 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.27 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.61 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.65 |
rpsA | 1834015 | c.474G>T | synonymous_variant | 0.53 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.6 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.29 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.32 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.23 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.68 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.32 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.22 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.65 |
rpsA | 1834063 | c.522C>T | synonymous_variant | 0.31 |
rpsA | 1834066 | c.525G>A | synonymous_variant | 0.25 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.31 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.53 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.21 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.18 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.27 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.2 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.3 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.18 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.18 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.18 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.18 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.2 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.3 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.21 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.31 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.27 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.18 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.35 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.35 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.31 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.23 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.19 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.19 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.23 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.2 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.29 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.31 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.31 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.31 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.31 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.18 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.27 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.33 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.25 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.22 |
rpsA | 1834397 | p.His286Asp | missense_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.5 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.33 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.33 |
rpsA | 1834523 | p.Glu328Gln | missense_variant | 0.33 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 0.4 |
rpsA | 1834558 | c.1017_1018insAAG | conservative_inframe_insertion | 0.4 |
rpsA | 1834570 | p.Asp343Glu | missense_variant | 0.4 |
rpsA | 1834572 | p.Ala344Val | missense_variant | 0.4 |
rpsA | 1834574 | p.Met345Phe | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2222895 | c.270C>A | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066045 | c.147T>C | synonymous_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.18 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.2 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.29 |
clpC1 | 4039711 | c.991_993delTAC | conservative_inframe_deletion | 0.33 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.33 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.33 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.33 |
clpC1 | 4039742 | c.963C>G | synonymous_variant | 0.33 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.33 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.33 |
clpC1 | 4039754 | c.951G>C | synonymous_variant | 0.33 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.4 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.67 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.67 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.67 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.67 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.75 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.75 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.67 |
clpC1 | 4039801 | p.Ile302Val | missense_variant | 0.67 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.67 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.75 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.6 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.5 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.33 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.29 |
clpC1 | 4039858 | p.Ile283Val | missense_variant | 0.29 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.29 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.29 |
clpC1 | 4039877 | p.Ile276Val | missense_variant | 0.29 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.25 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.25 |
clpC1 | 4040828 | c.-124T>A | upstream_gene_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
aftB | 4269540 | c.-704C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |