Run ID: ERR4814976
Sample name:
Date: 01-04-2023 13:35:52
Number of reads: 28553
Percentage reads mapped: 3.38
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 | 0.99 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 1.0 |
gyrA | 6787 | c.-515G>A | upstream_gene_variant | 1.0 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
gyrB | 6798 | p.Gly520Glu | missense_variant | 1.0 |
gyrA | 6820 | c.-482C>T | upstream_gene_variant | 1.0 |
gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
gyrA | 7568 | c.267_268insA | frameshift_variant | 1.0 |
gyrA | 7571 | c.271delT | frameshift_variant | 1.0 |
gyrA | 7574 | c.273G>T | synonymous_variant | 1.0 |
gyrA | 7577 | c.276C>T | synonymous_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7587 | p.Leu96Met | missense_variant | 1.0 |
gyrA | 7601 | c.300C>G | synonymous_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
gyrA | 7613 | c.312G>C | synonymous_variant | 1.0 |
gyrA | 7614 | p.Leu105Met | missense_variant | 1.0 |
gyrA | 7622 | c.321C>T | synonymous_variant | 1.0 |
gyrA | 7628 | c.327G>T | synonymous_variant | 1.0 |
gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
gyrA | 7637 | c.336C>T | synonymous_variant | 1.0 |
gyrA | 7643 | c.342C>T | synonymous_variant | 1.0 |
rpoB | 760199 | c.393C>G | synonymous_variant | 1.0 |
rpoB | 760207 | p.Ile134Thr | missense_variant | 1.0 |
rpoB | 760212 | p.Asn136Arg | missense_variant | 1.0 |
rpoB | 760215 | p.Asn137Glu | missense_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
rpoB | 760241 | c.435G>C | synonymous_variant | 1.0 |
rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
rpoB | 760250 | p.Met148Ile | missense_variant | 1.0 |
rpoB | 762840 | p.Pro1012Lys | missense_variant | 0.83 |
rpoB | 762850 | p.Tyr1015Phe | missense_variant | 0.9 |
rpoC | 762857 | c.-513C>T | upstream_gene_variant | 0.9 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.9 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.91 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.92 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.92 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.93 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.94 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.94 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.94 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.94 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.94 |
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 | 0.93 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.93 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.93 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.93 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.93 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.93 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.94 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.95 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.95 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.94 |
rpoC | 763058 | c.-312C>T | upstream_gene_variant | 1.0 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
rpoC | 763079 | c.-291C>T | upstream_gene_variant | 1.0 |
rpoC | 763082 | c.-288C>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 | 1.0 |
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>T | upstream_gene_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 | 764329 | c.960C>T | synonymous_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
rpoC | 764374 | c.1005C>T | synonymous_variant | 1.0 |
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 | 764428 | c.1059G>C | synonymous_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 | 764623 | c.1254C>G | synonymous_variant | 1.0 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 1.0 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 1.0 |
rpoC | 764659 | c.1290C>T | synonymous_variant | 1.0 |
rpoC | 764660 | p.Val431Ile | missense_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
rpsL | 781749 | p.Thr64Ser | missense_variant | 1.0 |
rpsL | 781754 | c.195G>T | synonymous_variant | 1.0 |
rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
rpsL | 781766 | c.207C>T | 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>T | 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 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800621 | c.-188G>A | upstream_gene_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 |
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 | 1472075 | n.230A>G | 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 | 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 | 1.0 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 1.0 |
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 | 1.0 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 1.0 |
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 | 0.99 |
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 | 1473287 | n.1442C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473668 | n.11C>G | 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 | 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 | 1.0 |
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 | 1.0 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474287 | n.630T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474288 | n.631C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474289 | n.632C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474293 | n.637_649delCCTCTCCGGAGGA | 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 | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 0.98 |
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 | 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 | 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 | 0.95 |
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 | 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 | 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 | 1475599 | n.1942A>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 | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475757 | n.2100_2101insG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112_2113insC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
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 | 1.0 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.96 |
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 | 1.0 |
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 | 1.0 |
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 |
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 | 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 | 0.9 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.9 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.89 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.88 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.88 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.88 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.75 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.4 |
rpsA | 1833877 | c.336C>T | synonymous_variant | 0.75 |
rpsA | 1833893 | p.Ala118Gln | missense_variant | 0.75 |
rpsA | 1833907 | p.Lys122Asn | missense_variant | 0.75 |
rpsA | 1833913 | c.372G>A | synonymous_variant | 0.67 |
rpsA | 1833914 | p.Ala125Pro | missense_variant | 0.67 |
rpsA | 1833919 | c.378C>T | synonymous_variant | 0.67 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.67 |
rpsA | 1833925 | c.384C>T | synonymous_variant | 0.67 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.67 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.78 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.92 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.92 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.92 |
rpsA | 1833991 | c.450C>T | synonymous_variant | 0.92 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.92 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.92 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.93 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.94 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.94 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.94 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.95 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834040 | p.Lys167Gln | missense_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 | 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 | 1.0 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 1.0 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 1.0 |
rpsA | 1834343 | p.Asp268Asn | missense_variant | 1.0 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 1.0 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>C | synonymous_variant | 1.0 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
rpsA | 1834375 | c.834G>T | synonymous_variant | 1.0 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 1.0 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
rpsA | 1834397 | p.His286Val | missense_variant | 1.0 |
rpsA | 1834417 | c.876G>A | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 1.0 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834504 | c.963G>T | synonymous_variant | 1.0 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.86 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.86 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.86 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.86 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.86 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.86 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.86 |
rpsA | 1834636 | c.1095C>T | synonymous_variant | 0.86 |
rpsA | 1834637 | p.Asn366Asp | missense_variant | 0.86 |
rpsA | 1834647 | p.Tyr369Phe | missense_variant | 0.88 |
rpsA | 1834654 | c.1113G>A | synonymous_variant | 0.88 |
rpsA | 1834667 | p.Ala376Thr | missense_variant | 0.88 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
clpC1 | 4038860 | c.1845G>C | 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>T | synonymous_variant | 1.0 |
clpC1 | 4038929 | c.1776G>T | synonymous_variant | 1.0 |
clpC1 | 4038932 | c.1773G>T | synonymous_variant | 1.0 |
clpC1 | 4038935 | c.1770C>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 | 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 | 4039856 | c.849C>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 |