Run ID: ERR4816852
Sample name:
Date: 01-04-2023 14:39:55
Number of reads: 60396
Percentage reads mapped: 4.28
Strain: lineage4.9
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
| gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrA | 6778 | c.-524C>T | upstream_gene_variant | 1.0 |
| gyrB | 6798 | p.Gly520Glu | missense_variant | 1.0 |
| gyrA | 6820 | c.-482C>T | upstream_gene_variant | 1.0 |
| gyrA | 6835 | c.-467C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 8294 | c.993T>G | synonymous_variant | 1.0 |
| gyrA | 8304 | p.Thr335Ser | missense_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8327 | c.1026C>T | synonymous_variant | 1.0 |
| gyrA | 8330 | c.1029C>G | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>C | synonymous_variant | 1.0 |
| gyrA | 8342 | c.1041G>C | synonymous_variant | 1.0 |
| gyrA | 8354 | c.1053G>T | synonymous_variant | 1.0 |
| gyrA | 8360 | c.1059G>A | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760241 | c.435G>T | synonymous_variant | 1.0 |
| rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
| rpoB | 760250 | p.Met148Ile | missense_variant | 1.0 |
| rpoB | 760271 | c.465C>G | synonymous_variant | 1.0 |
| rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
| rpoB | 760280 | c.474C>T | synonymous_variant | 1.0 |
| rpoB | 760290 | p.Ile162Val | missense_variant | 1.0 |
| rpoB | 760298 | c.492G>A | synonymous_variant | 1.0 |
| rpoB | 760301 | c.495C>T | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760313 | c.507G>T | synonymous_variant | 1.0 |
| rpoB | 760316 | c.510C>T | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_513delAGCinsTCT | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760334 | c.528G>T | synonymous_variant | 1.0 |
| rpoB | 760337 | c.531C>G | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>C | synonymous_variant | 1.0 |
| rpoB | 760343 | c.537G>C | synonymous_variant | 1.0 |
| rpoB | 760352 | c.546C>T | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 762795 | p.Asp997Asn | missense_variant | 1.0 |
| rpoC | 762800 | c.-570C>T | upstream_gene_variant | 1.0 |
| rpoC | 762806 | c.-564C>T | upstream_gene_variant | 1.0 |
| rpoB | 762814 | p.Met1003Thr | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-537delAGCinsTCT | upstream_gene_variant | 1.0 |
| rpoC | 762839 | c.-531G>A | upstream_gene_variant | 1.0 |
| rpoB | 762840 | p.Pro1012Lys | missense_variant | 1.0 |
| rpoB | 762850 | p.Tyr1015Phe | missense_variant | 1.0 |
| rpoC | 762857 | c.-513C>T | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
| rpoB | 762878 | p.Ile1024Met | missense_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoB | 762905 | p.Asp1033Glu | missense_variant | 1.0 |
| rpoC | 762911 | c.-459C>T | upstream_gene_variant | 1.0 |
| rpoC | 762917 | c.-453C>T | upstream_gene_variant | 1.0 |
| rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762938 | c.-432G>C | upstream_gene_variant | 1.0 |
| rpoC | 762944 | c.-426C>T | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>T | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoB | 763005 | p.Cys1067Gly | missense_variant | 0.95 |
| rpoC | 763013 | c.-357C>A | upstream_gene_variant | 1.0 |
| rpoC | 763022 | c.-348C>A | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763079 | c.-291C>T | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>A | upstream_gene_variant | 1.0 |
| rpoC | 763109 | c.-261C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoB | 763118 | p.Glu1104Asp | missense_variant | 1.0 |
| rpoC | 763124 | c.-246C>T | upstream_gene_variant | 1.0 |
| rpoB | 763130 | p.Glu1108Asp | missense_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.96 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>T | upstream_gene_variant | 1.0 |
| rpoC | 763163 | c.-207C>G | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763181 | c.-189G>C | upstream_gene_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763462 | c.93G>C | synonymous_variant | 1.0 |
| rpoC | 763471 | c.102C>T | synonymous_variant | 1.0 |
| rpoC | 763480 | c.111C>T | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763495 | c.126G>A | synonymous_variant | 1.0 |
| rpoC | 763501 | c.132C>T | synonymous_variant | 1.0 |
| rpoC | 763507 | c.138G>T | synonymous_variant | 1.0 |
| rpoC | 763513 | c.144C>T | synonymous_variant | 1.0 |
| rpoC | 763517 | p.Lys50Arg | missense_variant | 1.0 |
| rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763537 | c.168C>T | synonymous_variant | 1.0 |
| rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
| rpoC | 763558 | c.189C>T | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>T | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763597 | c.228G>A | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763609 | c.240C>T | synonymous_variant | 1.0 |
| rpoC | 763630 | c.261G>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
| rpoC | 763654 | c.285C>T | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>T | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>C | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>T | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
| rpoC | 763769 | p.Tyr134Asn | missense_variant | 1.0 |
| rpoC | 763772 | p.Val135Ile | missense_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 0.88 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 0.88 |
| rpoC | 764374 | c.1005C>T | synonymous_variant | 0.88 |
| rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764383 | c.1014C>G | synonymous_variant | 1.0 |
| rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
| rpoC | 764404 | c.1035C>T | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764419 | c.1050C>A | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764438 | p.Leu357Met | missense_variant | 1.0 |
| rpoC | 764443 | c.1074C>T | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764455 | c.1086G>T | synonymous_variant | 1.0 |
| rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>T | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>T | synonymous_variant | 1.0 |
| rpoC | 764509 | c.1140G>A | synonymous_variant | 1.0 |
| rpoC | 764515 | c.1146C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>A | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764530 | c.1161C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764545 | c.1176C>T | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
| rpoC | 764554 | c.1185C>T | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 0.88 |
| rpoC | 764572 | c.1203G>C | synonymous_variant | 0.88 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.88 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 0.91 |
| rpoC | 764602 | c.1233C>T | synonymous_variant | 0.95 |
| rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764623 | c.1254C>G | synonymous_variant | 0.94 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764635 | c.1266C>T | synonymous_variant | 0.92 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 0.92 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>T | synonymous_variant | 0.92 |
| rpoC | 764659 | c.1290C>T | synonymous_variant | 0.92 |
| rpoC | 764660 | p.Val431Ile | missense_variant | 0.92 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 0.94 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>T | synonymous_variant | 1.0 |
| rpoC | 764716 | c.1347G>T | synonymous_variant | 1.0 |
| rpoC | 764737 | c.1368G>T | synonymous_variant | 1.0 |
| rpoC | 764744 | p.Arg459Glu | missense_variant | 1.0 |
| rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
| rpoC | 764754 | p.Asp462Ala | missense_variant | 1.0 |
| rpoC | 764756 | p.Leu463Lys | missense_variant | 1.0 |
| rpoC | 764760 | p.Asn464Ser | missense_variant | 1.0 |
| rpoC | 764762 | p.His465Tyr | missense_variant | 1.0 |
| rpoC | 764785 | c.1416C>G | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>T | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>A | synonymous_variant | 1.0 |
| rpoC | 764813 | p.Gln482Glu | missense_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764836 | p.Glu489Asp | missense_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>T | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764896 | c.1527C>T | synonymous_variant | 1.0 |
| rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Val | missense_variant | 1.0 |
| rpoC | 764920 | c.1551G>T | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764926 | c.1557C>T | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764947 | c.1578G>A | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764952 | p.Val528Ala | missense_variant | 1.0 |
| rpoC | 764962 | c.1593G>T | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>A | synonymous_variant | 1.0 |
| rpoC | 764998 | c.1629G>T | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>T | synonymous_variant | 1.0 |
| rpoC | 765022 | c.1653G>A | synonymous_variant | 1.0 |
| rpoC | 765038 | p.Ile557Val | missense_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 765064 | c.1695C>T | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>T | synonymous_variant | 1.0 |
| rpoC | 766300 | c.2931C>G | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>T | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766321 | c.2952C>A | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>A | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766351 | c.2982C>T | synonymous_variant | 1.0 |
| rpoC | 766357 | c.2988C>T | synonymous_variant | 1.0 |
| rpoC | 766360 | c.2991C>T | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766366 | c.2997C>T | synonymous_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766378 | c.3009C>T | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766387 | c.3018C>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766434 | p.Glu1022Gly | missense_variant | 1.0 |
| rpoC | 766441 | c.3072C>T | synonymous_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>T | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>T | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781805 | c.246G>C | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781820 | c.261G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781851 | p.Ile98Val | missense_variant | 1.0 |
| rpsL | 781856 | c.297C>T | synonymous_variant | 1.0 |
| rpsL | 781862 | c.303G>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781884 | p.Asn109Asp | missense_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781901 | c.342C>T | synonymous_variant | 1.0 |
| rpsL | 781902 | c.343_344delAGinsTC | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>A | synonymous_variant | 1.0 |
| rplC | 800630 | c.-179G>T | upstream_gene_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800639 | c.-170C>T | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>T | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>T | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800714 | c.-95C>T | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>A | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800741 | c.-68C>T | upstream_gene_variant | 1.0 |
| rplC | 800744 | c.-65G>A | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>T | upstream_gene_variant | 1.0 |
| rplC | 800756 | c.-53C>T | upstream_gene_variant | 1.0 |
| rplC | 800768 | c.-41C>A | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800777 | c.-32C>T | upstream_gene_variant | 1.0 |
| rplC | 800780 | c.-29C>G | upstream_gene_variant | 1.0 |
| rplC | 800786 | c.-23C>T | upstream_gene_variant | 1.0 |
| rrs | 1471858 | n.13A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.186_187insTGTG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472036 | n.192_197delATGTCT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472057 | n.212C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472297 | n.454_457delTCCG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472304 | n.459G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472307 | n.464_471delCTCGGATT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472325 | n.480G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472843 | n.998_999insT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1003delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472993 | n.1148G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473097 | n.1252G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473100 | n.1255G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473122 | n.1277T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473697 | n.40C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473700 | n.43G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473701 | n.44A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473718 | n.61G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473751 | n.94C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473911 | n.254G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473918 | n.261C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474112 | n.455T>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 | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474178 | n.522dupC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474289 | n.633_647delTTTTCCTCTCCGGAG | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1474374 | n.717_718insTTG | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 0.95 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.89 |
| rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.94 |
| rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1097delC | 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 | 1.0 |
| rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474952 | n.1295_1296insAT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475094 | n.1437C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475137 | n.1480A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475201 | n.1544G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475212 | n.1555A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475223 | n.1566G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475442 | n.1785C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475485 | n.1828C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475514 | n.1857G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475756 | n.2101_2108delACCCGCAA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476029 | n.2372A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476091 | n.2434_2435insC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476194 | n.2537A>G | 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 | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476269 | n.2612C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476274 | n.2617G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476523 | n.2867delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476600 | n.2943A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476675 | n.3018C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476684 | n.3027C>T | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833631 | p.Ile30Met | missense_variant | 1.0 |
| rpsA | 1833649 | c.108C>T | synonymous_variant | 1.0 |
| rpsA | 1833658 | c.117C>T | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833668 | p.Ile43Val | missense_variant | 1.0 |
| rpsA | 1833673 | c.132C>T | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>T | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>T | synonymous_variant | 1.0 |
| rpsA | 1833718 | c.177C>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833730 | c.189C>T | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833769 | c.228C>T | synonymous_variant | 1.0 |
| rpsA | 1833770 | p.Asn77Asp | missense_variant | 1.0 |
| rpsA | 1833823 | c.282G>A | synonymous_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833877 | c.336C>T | synonymous_variant | 1.0 |
| rpsA | 1833893 | p.Ala118Gln | missense_variant | 1.0 |
| rpsA | 1833907 | p.Lys122Asn | missense_variant | 1.0 |
| rpsA | 1833914 | p.Ala125Pro | missense_variant | 1.0 |
| rpsA | 1833919 | c.378C>T | synonymous_variant | 1.0 |
| rpsA | 1833921 | p.Lys127Thr | missense_variant | 1.0 |
| rpsA | 1833925 | c.384C>T | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833934 | c.393C>T | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833983 | c.442C>T | synonymous_variant | 1.0 |
| rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>T | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>T | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834024 | c.483G>C | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
| rpsA | 1834048 | c.507C>T | synonymous_variant | 1.0 |
| rpsA | 1834069 | c.528G>C | synonymous_variant | 1.0 |
| rpsA | 1834090 | c.549G>C | synonymous_variant | 1.0 |
| rpsA | 1834093 | c.552G>T | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>A | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
| rpsA | 1834129 | c.588C>T | synonymous_variant | 1.0 |
| rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
| rpsA | 1834139 | c.598_599delAGinsTC | synonymous_variant | 1.0 |
| rpsA | 1834172 | p.Ile211Val | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>T | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>A | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>T | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>T | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834252 | c.711C>T | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 0.98 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 0.98 |
| rpsA | 1834327 | c.786G>T | synonymous_variant | 0.98 |
| rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.98 |
| rpsA | 1834340 | p.Met267Leu | missense_variant | 0.98 |
| rpsA | 1834343 | p.Asp268Asn | missense_variant | 0.98 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 0.98 |
| rpsA | 1834354 | c.813G>C | synonymous_variant | 0.98 |
| rpsA | 1834360 | c.819G>C | synonymous_variant | 0.96 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 0.96 |
| rpsA | 1834366 | c.825A>C | synonymous_variant | 0.96 |
| rpsA | 1834369 | c.828C>G | synonymous_variant | 0.96 |
| rpsA | 1834375 | c.834G>T | synonymous_variant | 0.96 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 0.96 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 0.95 |
| rpsA | 1834397 | p.His286Val | missense_variant | 0.95 |
| rpsA | 1834402 | c.861C>T | synonymous_variant | 0.95 |
| rpsA | 1834417 | c.876G>A | synonymous_variant | 0.95 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 0.97 |
| rpsA | 1834429 | c.888C>T | synonymous_variant | 0.9 |
| rpsA | 1834432 | c.891G>A | synonymous_variant | 0.95 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834486 | c.945G>A | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834504 | c.963G>T | synonymous_variant | 1.0 |
| rpsA | 1834591 | c.1050C>T | synonymous_variant | 1.0 |
| rpsA | 1834600 | c.1059G>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>T | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834624 | c.1083G>C | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834636 | c.1095C>T | synonymous_variant | 1.0 |
| rpsA | 1834637 | p.Asn366Asp | missense_variant | 1.0 |
| rpsA | 1834647 | p.Tyr369Phe | missense_variant | 1.0 |
| rpsA | 1834654 | c.1113G>A | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Thr | missense_variant | 1.0 |
| rpsA | 1834683 | p.Ala381Gly | missense_variant | 1.0 |
| rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| fbiB | 3642232 | c.699delG | frameshift_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878358 | c.150C>A | synonymous_variant | 1.0 |
| rpoA | 3878361 | c.147G>T | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878373 | c.135G>C | synonymous_variant | 1.0 |
| rpoA | 3878384 | c.124C>T | synonymous_variant | 1.0 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 1.0 |
| rpoA | 3878388 | c.120C>T | synonymous_variant | 1.0 |
| rpoA | 3878394 | c.114G>T | synonymous_variant | 1.0 |
| rpoA | 3878397 | c.111G>T | synonymous_variant | 1.0 |
| rpoA | 3878400 | c.108T>C | synonymous_variant | 1.0 |
| rpoA | 3878403 | c.105C>T | synonymous_variant | 1.0 |
| rpoA | 3878406 | c.102G>C | synonymous_variant | 1.0 |
| rpoA | 3878415 | c.93C>T | synonymous_variant | 1.0 |
| rpoA | 3878421 | c.87A>T | synonymous_variant | 1.0 |
| rpoA | 3878442 | c.66G>T | synonymous_variant | 1.0 |
| rpoA | 3878449 | p.Gln20Arg | missense_variant | 1.0 |
| rpoA | 3878454 | c.54A>C | synonymous_variant | 1.0 |
| clpC1 | 4038793 | c.1912C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038803 | c.1902C>T | synonymous_variant | 1.0 |
| clpC1 | 4038811 | p.Gln632Lys | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>C | synonymous_variant | 1.0 |
| clpC1 | 4038824 | c.1881C>T | synonymous_variant | 1.0 |
| clpC1 | 4038836 | c.1869G>T | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038857 | c.1848C>T | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038872 | c.1833C>T | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038890 | c.1815G>A | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>T | synonymous_variant | 1.0 |
| clpC1 | 4038917 | c.1788C>T | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>C | synonymous_variant | 1.0 |
| clpC1 | 4038926 | c.1779G>C | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>T | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038962 | c.1743C>T | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038977 | c.1728G>C | synonymous_variant | 1.0 |
| clpC1 | 4038983 | p.Asp574Glu | missense_variant | 1.0 |
| clpC1 | 4038986 | p.Asp573Glu | missense_variant | 1.0 |
| clpC1 | 4038995 | c.1708_1710delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039001 | p.Asn568Glu | missense_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039010 | c.1695G>C | synonymous_variant | 1.0 |
| clpC1 | 4039016 | c.1689C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039034 | c.1671C>T | synonymous_variant | 1.0 |
| clpC1 | 4039058 | c.1647C>T | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
| clpC1 | 4039094 | c.1611C>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>T | synonymous_variant | 1.0 |
| clpC1 | 4039505 | p.Ile400Val | missense_variant | 1.0 |
| clpC1 | 4039508 | c.1197G>C | synonymous_variant | 1.0 |
| clpC1 | 4039514 | c.1191C>T | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039526 | c.1179G>C | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>T | synonymous_variant | 1.0 |
| clpC1 | 4039685 | c.1020C>T | synonymous_variant | 1.0 |
| clpC1 | 4039691 | c.1014G>T | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>T | synonymous_variant | 1.0 |
| clpC1 | 4039709 | c.996C>T | synonymous_variant | 1.0 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
| clpC1 | 4039718 | c.987C>T | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039727 | c.978C>T | synonymous_variant | 1.0 |
| clpC1 | 4039730 | c.973_975delCTCinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>T | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>T | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039784 | c.921C>T | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>A | synonymous_variant | 1.0 |
| clpC1 | 4039796 | c.909C>T | synonymous_variant | 1.0 |
| clpC1 | 4039799 | c.906C>T | synonymous_variant | 1.0 |
| clpC1 | 4039802 | c.903G>A | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>T | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
| clpC1 | 4039847 | c.858C>T | synonymous_variant | 1.0 |
| clpC1 | 4039871 | p.Thr278Gln | missense_variant | 1.0 |
| clpC1 | 4039877 | c.828C>T | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039901 | c.804C>T | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039925 | c.780C>T | synonymous_variant | 1.0 |
| clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>T | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | p.Thr249Ser | missense_variant | 1.0 |
| clpC1 | 4039964 | c.741C>T | synonymous_variant | 1.0 |
| clpC1 | 4039973 | c.732C>T | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
