Run ID: SRR3675230
Sample name:
Date: 04-04-2023 05:23:00
Number of reads: 349615
Percentage reads mapped: 13.91
Strain: lineage3
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.5 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.5 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.59 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.23 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6415 | c.-887G>T | upstream_gene_variant | 0.5 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9016 | p.Thr572Ser | missense_variant | 0.33 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.33 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620396 | p.Ser169Tyr | missense_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.25 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.38 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.43 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.38 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.38 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.38 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.44 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.44 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.44 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.44 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.44 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.2 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.56 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.62 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.57 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.62 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.62 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.57 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.6 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.6 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.5 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.5 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.5 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.4 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.18 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.25 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.27 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.29 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.29 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.33 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.33 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.41 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.44 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.44 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.38 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.41 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.41 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.41 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.44 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.47 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.38 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.2 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.43 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.3 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.3 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.3 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.3 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.3 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.17 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.23 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.23 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.14 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.25 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.24 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.3 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.29 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.35 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.17 |
rpoC | 762968 | c.-402G>A | upstream_gene_variant | 0.21 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.48 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.42 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.5 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.45 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.23 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.45 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.45 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.5 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.24 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.48 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.6 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.33 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.67 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.46 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.5 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.2 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.27 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.22 |
rpoC | 763480 | c.111C>T | synonymous_variant | 0.22 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.25 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.38 |
rpoC | 763504 | c.135C>G | synonymous_variant | 0.22 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.38 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.5 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.36 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.27 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.45 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.45 |
rpoC | 763558 | c.189C>G | synonymous_variant | 0.25 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.18 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.45 |
rpoC | 763588 | c.219C>T | synonymous_variant | 0.27 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.33 |
rpoC | 763600 | c.231C>G | synonymous_variant | 0.4 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.5 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.44 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.44 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.22 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.56 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.27 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.33 |
rpoC | 763655 | p.Glu96Asn | missense_variant | 0.22 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.71 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.6 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.29 |
rpoC | 763672 | c.303C>A | synonymous_variant | 0.4 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.29 |
rpoC | 763681 | c.312C>T | synonymous_variant | 0.25 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.57 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.86 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.86 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.57 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.57 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.57 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.6 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.67 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.75 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.8 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.43 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.22 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.3 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.3 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.3 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.3 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.2 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.38 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.38 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.38 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.33 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.33 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.3 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.3 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.42 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.5 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.5 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.47 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.4 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.38 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.46 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.46 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.46 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.46 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.43 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.57 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.57 |
rpoC | 764681 | c.1312C>T | synonymous_variant | 0.38 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.35 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.5 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.38 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.44 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.33 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.25 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.17 |
rpoC | 764756 | p.Leu463Lys | missense_variant | 0.17 |
rpoC | 764762 | p.His465Tyr | missense_variant | 0.2 |
rpoC | 764774 | p.Ile469Val | missense_variant | 0.22 |
rpoC | 764780 | p.Ser471Ala | missense_variant | 0.25 |
rpoC | 764793 | p.Met475Lys | missense_variant | 0.38 |
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 |
atpE | 1461082 | p.Gly13Ala | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472274 | n.429A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.57 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.34 |
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 | 0.61 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474326 | n.669T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474381 | n.724T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475079 | n.1422T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.27 |
rpsA | 1833641 | p.Asn34Asp | missense_variant | 0.14 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.14 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.31 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.31 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.38 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.36 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.36 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.23 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.2 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.33 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.19 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.33 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.36 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.36 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.36 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.15 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.38 |
rpsA | 1833775 | p.Glu78Asp | missense_variant | 0.15 |
rpsA | 1833776 | p.Val79Ile | missense_variant | 0.23 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.18 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.2 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.33 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.57 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.57 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.33 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.83 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.78 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.62 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.8 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.73 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.82 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.91 |
rpsA | 1834018 | c.477C>T | synonymous_variant | 0.17 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.73 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.58 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.17 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.67 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.83 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.23 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.69 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.58 |
rpsA | 1834066 | c.525G>A | synonymous_variant | 0.29 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.47 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.54 |
rpsA | 1834099 | c.558C>T | synonymous_variant | 0.23 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.36 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.2 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.31 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.38 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.4 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.44 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.29 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.35 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.33 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.33 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.27 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.27 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.28 |
rpsA | 1834333 | c.792C>T | synonymous_variant | 0.31 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.25 |
rpsA | 1834340 | p.Met267Phe | missense_variant | 0.27 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.41 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.36 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.44 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.41 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.47 |
rpsA | 1834366 | c.825A>C | synonymous_variant | 0.44 |
rpsA | 1834375 | c.834G>T | synonymous_variant | 0.31 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.4 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.19 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.33 |
rpsA | 1834397 | p.His286Ala | missense_variant | 0.25 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.86 |
Rv3083 | 3448488 | c.-16C>A | upstream_gene_variant | 0.33 |
Rv3083 | 3449555 | p.Gln351Arg | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877474 | p.Glu345Val | missense_variant | 0.33 |
ddn | 3986882 | c.39C>G | synonymous_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245188 | c.1956G>T | synonymous_variant | 0.25 |
embB | 4246325 | c.-189G>A | upstream_gene_variant | 0.25 |
ubiA | 4269989 | c.-156G>T | upstream_gene_variant | 0.22 |
ethA | 4326226 | c.1248C>T | synonymous_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |