Run ID: SRR1173385
Sample name:
Date: 03-04-2023 03:23:24
Number of reads: 11406
Percentage reads mapped: 2.46
Strain: lineage4.9
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 1.0 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 1.0 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 1.0 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 1.0 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
rpoB | 762057 | p.Ile751Val | missense_variant | 1.0 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 1.0 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 1.0 |
rpoB | 762175 | c.2369_2370insCG | frameshift_variant | 1.0 |
rpoB | 762179 | c.2374_2375delGA | frameshift_variant | 1.0 |
rpoB | 762185 | c.2379G>T | synonymous_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 | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
rpoB | 762909 | p.Ile1035Leu | missense_variant | 1.0 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>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>T | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>T | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>T | synonymous_variant | 1.0 |
rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763711 | c.342G>C | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764440 | c.1071G>C | 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 | 764458 | c.1089G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 1.0 |
rpoC | 764563 | c.1194G>C | synonymous_variant | 1.0 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 1.0 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
rpoC | 764705 | p.Leu446Ala | missense_variant | 1.0 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764768 | p.Gln467Lys | missense_variant | 0.33 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
rpsL | 781772 | c.213C>A | synonymous_variant | 1.0 |
rpsL | 781793 | c.234G>C | synonymous_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 | 781832 | c.273T>G | synonymous_variant | 1.0 |
rpsL | 781838 | c.279G>T | synonymous_variant | 1.0 |
rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
rplC | 800643 | c.-166_-164delCGCinsAAG | 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 | 800669 | c.-140G>T | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 1.0 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 1.0 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
rplC | 800742 | c.-67G>T | upstream_gene_variant | 1.0 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
rplC | 800753 | c.-56C>T | upstream_gene_variant | 1.0 |
rplC | 800754 | c.-55A>C | upstream_gene_variant | 1.0 |
rplC | 800762 | c.-47T>C | upstream_gene_variant | 1.0 |
rplC | 800769 | c.-40A>G | upstream_gene_variant | 1.0 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471980 | n.135G>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 | 1.0 |
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 | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473026 | n.1181T>C | 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 | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473109 | n.1264T>C | 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 | 1473120 | n.1275C>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 | 1.0 |
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 | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473202 | n.1357C>T | 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 | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473702 | n.45G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473725 | n.68G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473732 | n.75G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473735 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473765 | n.108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473768 | n.111A>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 | 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 | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474317 | n.660G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474348 | n.691C>T | 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 | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474381 | n.724T>A | 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 | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | 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 | 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>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 | 1474651 | n.995delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474662 | n.1005C>G | 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 | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474690 | n.1033C>T | 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 | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>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 | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
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 | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475532 | n.1875A>G | 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 | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | 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 | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475982 | n.2325G>A | 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 | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476126 | n.2469C>T | 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 | 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 | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476255 | n.2598A>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 | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | 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 | 0.75 |
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 | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>A | 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 | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | 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 | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476601 | n.2944G>A | 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 | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834327 | c.786G>C | 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 | 1834360 | c.819G>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 | 1834399 | p.His286Gln | missense_variant | 1.0 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
rpoA | 3877968 | c.540C>G | synonymous_variant | 1.0 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
rpoA | 3877983 | c.525C>G | synonymous_variant | 1.0 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 1.0 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 1.0 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
clpC1 | 4039442 | c.1263A>C | synonymous_variant | 1.0 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
clpC1 | 4039481 | p.Ala408Ser | missense_variant | 1.0 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
clpC1 | 4039647 | p.Glu353Pro | missense_variant | 1.0 |
clpC1 | 4039651 | p.Val352Leu | missense_variant | 1.0 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 1.0 |
clpC1 | 4039661 | p.Gly348Ala | missense_variant | 1.0 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 1.0 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 1.0 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
clpC1 | 4040081 | c.624C>G | synonymous_variant | 1.0 |
clpC1 | 4040084 | c.621C>G | synonymous_variant | 1.0 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 1.0 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |