Run ID: ERR4820410
Sample name:
Date: 01-04-2023 16:40:02
Number of reads: 467164
Percentage reads mapped: 21.2
Strain: lineage3.1.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7572 | p.Ser91Ala | missense_variant | 0.5 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.7 | rifampicin |
rpoB | 761185 | p.Glu460Gly | missense_variant | 0.14 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.35 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6142 | c.903G>C | synonymous_variant | 1.0 |
gyrB | 6170 | p.His311Thr | missense_variant | 0.67 |
gyrB | 6175 | c.936G>A | synonymous_variant | 0.67 |
gyrB | 6183 | p.Thr315Met | missense_variant | 0.67 |
gyrB | 6190 | c.951A>G | synonymous_variant | 0.67 |
gyrB | 6204 | p.Ser322Thr | missense_variant | 0.67 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.67 |
gyrB | 6302 | p.Ala355Thr | missense_variant | 0.67 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.67 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.67 |
gyrB | 6323 | p.Val362Leu | missense_variant | 0.67 |
gyrB | 6327 | p.Ser363Thr | missense_variant | 0.67 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.25 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.25 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.44 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.22 |
gyrA | 7591 | p.Val97Ala | missense_variant | 0.44 |
gyrA | 7596 | p.Met99Leu | missense_variant | 0.5 |
gyrA | 7600 | p.Ala100Val | missense_variant | 0.4 |
gyrA | 7606 | p.Pro102Arg | missense_variant | 0.13 |
gyrA | 7613 | c.312G>C | synonymous_variant | 0.14 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.43 |
gyrA | 7628 | c.327G>C | synonymous_variant | 0.43 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.46 |
gyrA | 7633 | p.Asp111Ala | missense_variant | 0.58 |
gyrA | 7643 | c.342C>T | synonymous_variant | 0.23 |
gyrA | 7653 | p.Ser118Thr | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9791 | c.2490C>T | synonymous_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575919 | p.Gly191Asp | missense_variant | 0.12 |
ccsA | 620677 | p.Pro263Thr | missense_variant | 0.14 |
rpoB | 760318 | p.Ser171Ile | missense_variant | 0.25 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.18 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.18 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.39 |
rpoB | 761037 | c.1231_1233delTTGinsCTC | synonymous_variant | 0.58 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.5 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.63 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.55 |
rpoB | 761058 | p.Val418Thr | missense_variant | 0.15 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.69 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.88 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.85 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.69 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.86 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.67 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.67 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.53 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.53 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.4 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.21 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.25 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.25 |
rpoB | 761520 | p.Tyr572Leu | missense_variant | 0.17 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.25 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.25 |
rpoB | 761557 | p.Ala584Gly | missense_variant | 0.27 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.27 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.27 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.27 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.21 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.27 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.31 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.18 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.41 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.56 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.65 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.64 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.64 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.58 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.65 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.62 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.62 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.61 |
rpoB | 762104 | c.2298C>T | synonymous_variant | 0.43 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.68 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.63 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.27 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.38 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.44 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.41 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.41 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.21 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.35 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.35 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.35 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.41 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.59 |
rpoB | 762218 | c.2412T>A | synonymous_variant | 0.52 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.69 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.59 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.57 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.69 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.69 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.13 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.13 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.12 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.19 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.13 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.14 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.33 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.5 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.29 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.2 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.13 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.4 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.55 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.43 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.67 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.6 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.4 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.33 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.44 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.92 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.65 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.71 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.73 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.7 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.73 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.7 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.68 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.68 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.7 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.59 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.25 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.38 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.44 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.55 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.36 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.67 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.6 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.6 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.6 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.58 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.5 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.27 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.27 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.23 |
rpoC | 763606 | c.237C>A | synonymous_variant | 0.19 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.14 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.15 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.27 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.18 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.17 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.2 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.2 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.29 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.17 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.24 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.29 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.12 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.64 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.73 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.77 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.81 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.64 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.73 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.73 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.71 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.8 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.76 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.67 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.84 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.13 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.79 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.15 |
rpoC | 764322 | p.Pro318Gln | missense_variant | 0.12 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.17 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.6 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.67 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 0.7 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.7 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.7 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.7 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.7 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.75 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.76 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.77 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.77 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.78 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.83 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.81 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.75 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.88 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.89 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.82 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.79 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.2 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.2 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.15 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.71 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.24 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.47 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.46 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.61 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.12 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.38 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.35 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.47 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.47 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.23 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.59 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.65 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.69 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.16 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.41 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.65 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.14 |
rpoC | 764644 | c.1275G>T | synonymous_variant | 0.14 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.56 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.76 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.58 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.68 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.81 |
rpoC | 764664 | p.Val432Gly | missense_variant | 0.14 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.22 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.54 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.54 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.48 |
rpoC | 764703 | p.Lys445Ser | missense_variant | 0.21 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.53 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.53 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.31 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.15 |
rpoC | 765852 | p.Lys828Arg | missense_variant | 0.22 |
rpoC | 765907 | c.2538G>C | synonymous_variant | 0.33 |
rpoC | 765923 | p.Asn852Ala | missense_variant | 0.22 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.25 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.3 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.27 |
rpoC | 765958 | c.2589C>G | synonymous_variant | 0.3 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.27 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.27 |
rpoC | 765988 | c.2619G>C | synonymous_variant | 0.27 |
rpoC | 765991 | c.2622C>G | synonymous_variant | 0.2 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 0.2 |
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 |
rpsL | 781616 | c.57C>G | synonymous_variant | 0.17 |
rpsL | 781623 | p.Ala22Pro | missense_variant | 0.22 |
rpsL | 781628 | c.69T>G | synonymous_variant | 0.22 |
rpsL | 781638 | c.79_80delAGinsTC | synonymous_variant | 0.25 |
rpsL | 781643 | c.84G>C | synonymous_variant | 0.25 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.22 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.22 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.22 |
rpsL | 781667 | c.108C>T | synonymous_variant | 0.44 |
rpsL | 781682 | c.123T>G | synonymous_variant | 0.44 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.36 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.29 |
rpsL | 781709 | c.150G>A | synonymous_variant | 0.27 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.17 |
rpsL | 781740 | p.Val61Ile | missense_variant | 0.17 |
rpsL | 781745 | c.186G>A | synonymous_variant | 0.32 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.55 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.46 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.65 |
rpsL | 781768 | p.Glu70Val | missense_variant | 0.17 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.24 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.14 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.75 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.68 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.75 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.65 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.65 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.62 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.5 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.56 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.36 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.4 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.4 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.25 |
Rv1258c | 1407350 | c.-10C>T | upstream_gene_variant | 0.18 |
atpE | 1461063 | p.Ala7Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472023 | n.178G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472484 | n.639A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472682 | n.837T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473365 | n.1520C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.4 |
rrl | 1474123 | n.466A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474142 | n.485C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474143 | n.486T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474150 | n.493C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474270 | n.613T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474282 | n.625G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474326 | n.669T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474381 | n.724T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474405 | n.749delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474928 | n.1271C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475109 | n.1452C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475137 | n.1480A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475180 | n.1523G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475518 | n.1861A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475521 | n.1864T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475529 | n.1872A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475532 | n.1875A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475766 | n.2109_2110insCTTTTTGTT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476140 | n.2483T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476183 | n.2526A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476187 | n.2530T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476592 | n.2935G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476680 | n.3023T>C | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.2 |
rpsA | 1833649 | c.108C>T | synonymous_variant | 0.42 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.46 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.46 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.46 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.43 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.4 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.38 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.46 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.36 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.42 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.25 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.22 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.22 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.22 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.38 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.38 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.43 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.5 |
rpsA | 1833926 | p.Thr129Ser | missense_variant | 0.5 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.43 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.43 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.43 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.4 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.29 |
rpsA | 1834064 | p.Glu175* | stop_gained | 0.25 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.22 |
rpsA | 1834096 | c.555G>T | synonymous_variant | 0.22 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.22 |
rpsA | 1834108 | c.567C>T | synonymous_variant | 0.29 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.25 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.68 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.82 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.9 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.87 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.79 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.92 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.95 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.95 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.86 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.81 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.36 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.73 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.73 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.73 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.76 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.62 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.54 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.25 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.2 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.54 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.54 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.67 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.67 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.73 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.6 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.6 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.69 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.69 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.67 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.67 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.67 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.29 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.29 |
rpsA | 1834522 | c.981C>G | synonymous_variant | 0.25 |
rpsA | 1834523 | p.Glu328Gln | missense_variant | 0.44 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 0.4 |
rpsA | 1834552 | c.1013_1015delTTG | disruptive_inframe_deletion | 0.33 |
rpsA | 1834558 | c.1017_1018insAAG | conservative_inframe_insertion | 0.29 |
rpsA | 1834570 | p.Asp343Glu | missense_variant | 0.29 |
rpsA | 1834572 | p.Ala344Val | missense_variant | 0.29 |
rpsA | 1834574 | p.Met345Phe | missense_variant | 0.29 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.25 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.25 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.2 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.18 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.2 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102646 | p.Glu133Lys | missense_variant | 0.22 |
ndh | 2103081 | c.-39A>T | upstream_gene_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518868 | p.Glu252* | stop_gained | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
thyA | 3073874 | p.Ile200Val | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087621 | p.Ala268Thr | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038826 | p.Ile627Val | missense_variant | 0.18 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.2 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.22 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.22 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.2 |
clpC1 | 4038872 | c.1833C>G | synonymous_variant | 0.22 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.27 |
clpC1 | 4038890 | p.Glu605Asp | missense_variant | 0.27 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.27 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.29 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.25 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.25 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 0.25 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.22 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.15 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.15 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.15 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.27 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.33 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.3 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.3 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.38 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.22 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.29 |
clpC1 | 4040015 | p.Ala230Ser | missense_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.17 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 0.2 |
clpC1 | 4040057 | c.648C>G | synonymous_variant | 0.21 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.15 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.2 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.23 |
clpC1 | 4040096 | c.609G>C | synonymous_variant | 0.17 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4240458 | p.Gly199Val | missense_variant | 0.15 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248468 | p.Tyr652Cys | missense_variant | 0.17 |
aftB | 4266965 | c.1872A>G | synonymous_variant | 0.14 |
ubiA | 4269247 | p.Leu196Pro | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |