Run ID: ERR4769553
Sample name:
Date: 01-04-2023 06:44:16
Number of reads: 36517
Percentage reads mapped: 2.3
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.98 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.57 | rifampicin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.85 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.67 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.67 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.67 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.67 |
rpoB | 760959 | p.Val385Thr | missense_variant | 0.67 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.67 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.75 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.75 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.83 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.71 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.83 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.86 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.86 |
rpoB | 761013 | p.Val403Ile | missense_variant | 0.71 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.88 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.71 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.86 |
rpoB | 761046 | p.Ile414Val | missense_variant | 0.71 |
rpoB | 761051 | c.1245G>A | synonymous_variant | 0.83 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.86 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.86 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.83 |
rpoB | 761071 | p.Lys422Arg | missense_variant | 0.2 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.25 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.57 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.57 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.86 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.8 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.67 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.67 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.67 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.67 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.67 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.5 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.67 |
rpoB | 761196 | p.Leu464Val | missense_variant | 0.5 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.6 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.5 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.5 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.5 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.75 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.75 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.75 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.75 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.75 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.75 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.8 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.8 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 1.0 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.5 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 1.0 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 1.0 |
rpoB | 763077 | p.Val1091Leu | missense_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.5 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.5 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.67 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763551 | p.Tyr61Ser | missense_variant | 1.0 |
rpoC | 763570 | c.201G>A | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763585 | c.216C>A | synonymous_variant | 1.0 |
rpoC | 763589 | p.Ile74Val | missense_variant | 1.0 |
rpoC | 763609 | c.240C>G | 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 | 763666 | c.297G>C | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>C | synonymous_variant | 1.0 |
rpoC | 763703 | c.334_336delTCGinsAGC | 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 | 763720 | c.351G>C | synonymous_variant | 1.0 |
rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763727 | p.Leu120Met | missense_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>C | synonymous_variant | 1.0 |
rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.67 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.71 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.71 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.8 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.89 |
rpoC | 764740 | p.Met457Ile | missense_variant | 0.9 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
rpoC | 764750 | p.Val461Ile | missense_variant | 1.0 |
rpoC | 764760 | p.Asn464Ser | missense_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 1.0 |
rpoC | 764804 | p.Gln479Ser | missense_variant | 1.0 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.75 |
rpoC | 764837 | p.Val490Ile | missense_variant | 0.75 |
rpoC | 764843 | p.Ala492Arg | missense_variant | 0.67 |
rpoC | 764850 | p.His494Arg | missense_variant | 0.67 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 1.0 |
rpoC | 764857 | c.1488G>T | synonymous_variant | 0.67 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.8 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.8 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.8 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.8 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.8 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.8 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.8 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.8 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.8 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.67 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.67 |
rpsL | 781876 | p.Gly106Ala | missense_variant | 0.67 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.5 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.5 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.5 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.5 |
rpsL | 781921 | p.Lys121Met | missense_variant | 0.4 |
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 | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472256 | n.411T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472645 | n.800G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472666 | n.821G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.67 |
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 | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473083 | n.1238G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473128 | n.1283C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473134 | n.1289T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473289 | n.1444T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473291 | n.1446G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474601 | n.944C>T | 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 | 1474660 | n.1003G>A | 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 | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474770 | n.1113G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474778 | n.1121C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475084 | n.1427G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>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 | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.4 |
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 | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476080 | n.2423T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476127 | n.2470C>A | non_coding_transcript_exon_variant | 0.67 |
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 | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.3 |
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 | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.33 |
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 | 0.27 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.57 |
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 | 0.71 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.75 |
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 | 1476543 | n.2886G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.5 |
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 | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833649 | c.108C>A | synonymous_variant | 0.67 |
rpsA | 1833653 | p.Ile38Leu | missense_variant | 0.67 |
rpsA | 1833656 | p.Val39Ile | missense_variant | 0.67 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.67 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.67 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833677 | p.Val46Ile | missense_variant | 0.67 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.67 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.67 |
rpsA | 1833704 | p.Ile55Val | missense_variant | 0.67 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.67 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.67 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.67 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.67 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.67 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.67 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.67 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 0.67 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 1.0 |
rpsA | 1833771 | p.Asn77Thr | missense_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039931 | c.774T>A | synonymous_variant | 0.67 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.67 |
clpC1 | 4039937 | p.Val256Ile | missense_variant | 0.67 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.67 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.67 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.67 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.67 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.67 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.67 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.8 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.75 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.8 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.8 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.8 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.8 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.8 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.8 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.8 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.8 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.8 |
clpC1 | 4040083 | p.Thr208Ser | missense_variant | 1.0 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
clpC1 | 4040096 | p.Val203Ile | missense_variant | 1.0 |
clpC1 | 4040114 | p.Ile197Met | missense_variant | 1.0 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |