Run ID: SRR6046839
Sample name:
Date: 04-04-2023 12:24:02
Number of reads: 64967
Percentage reads mapped: 5.52
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 | 0.82 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8406 | p.Gln369Lys | missense_variant | 1.0 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.75 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.75 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.75 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.71 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.71 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.71 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.71 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.71 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.71 |
rpoB | 761276 | c.1470G>C | synonymous_variant | 1.0 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 1.0 |
rpoB | 761289 | p.Ser495Ala | missense_variant | 1.0 |
rpoB | 761292 | p.Val496Ser | missense_variant | 1.0 |
rpoB | 761296 | p.Tyr497Phe | missense_variant | 1.0 |
rpoB | 761299 | p.Ala498Gly | missense_variant | 1.0 |
rpoB | 761303 | c.1497G>C | synonymous_variant | 1.0 |
rpoB | 761304 | p.Val500Ile | missense_variant | 1.0 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 1.0 |
rpoB | 761322 | p.Ile506Val | missense_variant | 1.0 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
rpoB | 761928 | p.Ala708Ser | missense_variant | 1.0 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 1.0 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 1.0 |
rpoB | 761973 | p.His723Tyr | missense_variant | 1.0 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 1.0 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 1.0 |
rpoB | 762024 | p.Val740Thr | missense_variant | 1.0 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 1.0 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
rpoB | 762074 | c.2268C>G | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
rpoB | 762162 | p.Ile786Val | missense_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762189 | p.Ile795Leu | missense_variant | 1.0 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 1.0 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 1.0 |
rpoB | 762287 | c.2481C>A | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 1.0 |
rpoB | 762297 | p.Leu831Met | missense_variant | 1.0 |
rpoB | 762305 | c.2499G>T | synonymous_variant | 1.0 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 1.0 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.83 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.83 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.83 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.83 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.88 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.9 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.94 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.94 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.89 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.89 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.89 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.89 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 0.89 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.89 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.89 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
rpoC | 763462 | c.93G>C | synonymous_variant | 1.0 |
rpoC | 763465 | c.96G>A | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
rpoC | 763504 | c.135C>A | synonymous_variant | 1.0 |
rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763576 | c.207C>T | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
rpoC | 763618 | c.249C>G | synonymous_variant | 1.0 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
rpoC | 763625 | p.Lys86Ala | missense_variant | 1.0 |
rpoC | 763630 | c.261G>T | synonymous_variant | 1.0 |
rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>C | synonymous_variant | 1.0 |
rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>T | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
rpoC | 763796 | p.Met143Leu | missense_variant | 1.0 |
rpoC | 764326 | c.957G>C | synonymous_variant | 1.0 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 1.0 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 1.0 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 1.0 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>A | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 1.0 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 1.0 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 1.0 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 1.0 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
rpoC | 764759 | p.Asn464Glu | missense_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
rpoC | 764785 | c.1416C>G | synonymous_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 1.0 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 1.0 |
rpoC | 766846 | c.3477C>T | synonymous_variant | 1.0 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
rpsL | 781670 | c.111G>C | synonymous_variant | 1.0 |
rpsL | 781679 | c.120C>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
rpsL | 781721 | c.162C>T | synonymous_variant | 1.0 |
rpsL | 781728 | c.169_171delTTGinsCTC | synonymous_variant | 1.0 |
rpsL | 781738 | p.Gln60Leu | missense_variant | 1.0 |
rpsL | 781740 | c.181_182insCA | frameshift_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 | 781768 | p.Glu70Val | missense_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781829 | c.270G>T | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
rpsL | 781860 | p.Ser101Ala | missense_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.Asn109Gly | missense_variant | 1.0 |
rpsL | 781892 | p.Lys111Asn | missense_variant | 1.0 |
rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
rpsL | 781901 | c.342C>T | synonymous_variant | 1.0 |
rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
rrs | 1471853 | n.8T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472309 | n.464C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472310 | n.465T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472426 | n.581T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472495 | n.650C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>G | 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 | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472970 | n.1126delG | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472974 | n.1129A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472975 | n.1130T>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | 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>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474153 | n.496C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474166 | n.509G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474289 | n.633_647delTTTTCCTCTCCGGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474936 | n.1279C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475063 | n.1406A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475078 | n.1421T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475091 | n.1434G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475111 | n.1454G>A | 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 | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475173 | n.1516A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476100 | n.2443A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476113 | n.2456T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.96 |
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 | 1476213 | n.2556G>T | non_coding_transcript_exon_variant | 0.85 |
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 | 0.88 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476267 | n.2610G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476276 | n.2619C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>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 | 0.91 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476613 | n.2956G>A | 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 | 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 | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833664 | c.123C>T | synonymous_variant | 1.0 |
rpsA | 1833665 | p.Thr42Val | missense_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 1.0 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 1.0 |
rpsA | 1833988 | c.447C>T | synonymous_variant | 1.0 |
rpsA | 1833991 | c.450C>G | 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 | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.94 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.93 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 1.0 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 1.0 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 1.0 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 1.0 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
rpsA | 1834405 | c.864C>T | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 1.0 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 1.0 |
rpsA | 1834538 | p.Val333Leu | missense_variant | 1.0 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 1.0 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 1.0 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
rpsA | 1834751 | p.Leu404Met | missense_variant | 1.0 |
rpsA | 1834756 | c.1215G>A | synonymous_variant | 1.0 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
rpsA | 1834766 | p.Lys409Ala | missense_variant | 1.0 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 1.0 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
rpsA | 1834793 | c.1253delA | frameshift_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
rpoA | 3877625 | p.Asp295His | missense_variant | 1.0 |
rpoA | 3877629 | c.879C>G | synonymous_variant | 1.0 |
rpoA | 3877636 | p.Gln291Ser | missense_variant | 1.0 |
rpoA | 3877650 | c.858C>T | synonymous_variant | 1.0 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 1.0 |
rpoA | 3877667 | p.Ser281Ala | missense_variant | 1.0 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
rpoA | 3877672 | p.Thr279Ser | missense_variant | 1.0 |
rpoA | 3877677 | p.Ala277Ser | missense_variant | 1.0 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 1.0 |
rpoA | 3877689 | c.819C>T | synonymous_variant | 1.0 |
rpoA | 3877701 | p.Val269Ile | missense_variant | 1.0 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 1.0 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 1.0 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 1.0 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 1.0 |
clpC1 | 4039533 | p.Asn391Thr | missense_variant | 1.0 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 1.0 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
clpC1 | 4039763 | c.942C>T | synonymous_variant | 1.0 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 1.0 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
clpC1 | 4039793 | c.912C>T | synonymous_variant | 1.0 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 1.0 |
clpC1 | 4039805 | c.900C>G | synonymous_variant | 1.0 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4039833 | p.Thr291Ser | missense_variant | 1.0 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 1.0 |
clpC1 | 4039874 | p.Asn277Arg | missense_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 1.0 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 1.0 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
clpC1 | 4039949 | c.756G>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 | c.747G>C | synonymous_variant | 1.0 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245515 | c.-999C>T | upstream_gene_variant | 1.0 |