Run ID: ERR4818646
Sample name:
Date: 01-04-2023 15:40:25
Number of reads: 1183903
Percentage reads mapped: 22.19
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.36 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.39 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.4 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.36 |
gyrB | 6302 | p.Ala355Thr | missense_variant | 0.35 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.34 |
gyrB | 6308 | p.Val357Ile | missense_variant | 0.34 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.36 |
gyrB | 6323 | p.Val362Leu | missense_variant | 0.34 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.39 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.31 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 759888 | p.Gly28* | stop_gained | 0.15 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.13 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.12 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.27 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.34 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.38 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.5 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.59 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.65 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.65 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.65 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.74 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.76 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.66 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.66 |
rpoB | 761129 | c.1323G>T | synonymous_variant | 0.57 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.52 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.52 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.5 |
rpoB | 761147 | c.1341C>G | synonymous_variant | 0.46 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.47 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.44 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.42 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.37 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.38 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.18 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.18 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.16 |
rpoB | 761519 | c.1713C>T | synonymous_variant | 0.14 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.35 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.57 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.57 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.61 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.63 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.61 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.51 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.54 |
rpoB | 761622 | p.Gln606Met | missense_variant | 0.48 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.44 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.4 |
rpoB | 761643 | p.Val613Ile | missense_variant | 0.24 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 0.23 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.42 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.42 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.46 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.45 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.45 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.51 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.51 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.5 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.49 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.48 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.46 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 0.46 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.32 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.31 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.31 |
rpoB | 762098 | c.2292C>T | synonymous_variant | 0.35 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.36 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.48 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.61 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.65 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.58 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.58 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.59 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.65 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 0.67 |
rpoB | 762175 | c.2369_2370insCG | frameshift_variant | 0.67 |
rpoB | 762179 | c.2374_2375delGA | frameshift_variant | 0.61 |
rpoB | 762185 | c.2379G>T | synonymous_variant | 0.66 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.71 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.63 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.61 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.61 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.61 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.6 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.6 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.59 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 0.56 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.53 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 0.17 |
rpoB | 762426 | p.Ser874Thr | missense_variant | 0.12 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.14 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.24 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.3 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.33 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.31 |
rpoC | 762866 | c.-504C>G | upstream_gene_variant | 0.42 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.53 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.55 |
rpoB | 762909 | p.Ile1035Leu | missense_variant | 0.56 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.56 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.54 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.55 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.43 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.32 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.27 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.28 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.28 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.45 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.44 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.54 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.57 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.56 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.58 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.58 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.53 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.49 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.49 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.47 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.34 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.14 |
rpoB | 763161 | p.Leu1119Ile | missense_variant | 0.14 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.14 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.14 |
rpoB | 763170 | p.Leu1122Met | missense_variant | 0.14 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 0.15 |
rpoC | 763455 | c.87A>G | synonymous_variant | 0.25 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.31 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.39 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.56 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.57 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.63 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.63 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.67 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.66 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.65 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.66 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.66 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.65 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.68 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.72 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.74 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.67 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.68 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.66 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.61 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.49 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.51 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.51 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.54 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.54 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.54 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.56 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.55 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.46 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.33 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.28 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.24 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.17 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.19 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.38 |
rpoC | 763947 | p.Ala193Val | missense_variant | 0.38 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.4 |
rpoC | 763960 | c.591T>G | synonymous_variant | 0.43 |
rpoC | 763966 | p.Asp199Glu | missense_variant | 0.43 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.4 |
rpoC | 763971 | p.Gly201Ala | missense_variant | 0.4 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.21 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 0.48 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.54 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.56 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.56 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.56 |
rpoC | 764440 | c.1071G>T | synonymous_variant | 0.56 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.56 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.54 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.54 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.57 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.58 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.58 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.55 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.46 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.38 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.53 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.57 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.56 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.61 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.6 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.59 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.61 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.66 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.68 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.68 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.69 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.69 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.72 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.63 |
rpoC | 764646 | p.Gly426Ala | missense_variant | 0.52 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.49 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.48 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.48 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.51 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.53 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.59 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.57 |
rpoC | 764705 | p.Leu446Ala | missense_variant | 0.54 |
rpoC | 764734 | c.1365C>T | synonymous_variant | 0.47 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.46 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.45 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.4 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.44 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.36 |
rpoC | 764804 | p.Gln479Gly | missense_variant | 0.36 |
rpoC | 764810 | p.Pro481Thr | missense_variant | 0.35 |
rpoC | 764813 | p.Gln482Val | missense_variant | 0.35 |
rpoC | 764820 | p.Trp484Tyr | missense_variant | 0.34 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.38 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.37 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.37 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.15 |
rpoC | 764971 | c.1602C>G | synonymous_variant | 0.18 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.24 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.24 |
rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 0.24 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.26 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.26 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.25 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.25 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.26 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.26 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.26 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777043 | c.1438C>A | synonymous_variant | 0.14 |
mmpR5 | 779217 | c.230_231delTT | frameshift_variant | 0.13 |
mmpR5 | 779393 | p.Arg135Gln | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.41 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.51 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.53 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.64 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.67 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.66 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.61 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.62 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.6 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.6 |
rpsL | 781856 | c.297C>T | synonymous_variant | 0.42 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.45 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.4 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.4 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.4 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.45 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.4 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.2 |
rplC | 800644 | c.-165G>A | upstream_gene_variant | 0.13 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471917 | n.72G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1471991 | n.146T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1471998 | n.153G>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472005 | n.160T>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472023 | n.178G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472673 | n.828T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472675 | n.830T>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472863 | n.1018T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1473392 | n.-266C>T | upstream_gene_variant | 0.2 |
rrl | 1473666 | n.9G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473702 | n.45G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473735 | n.78T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473744 | n.87T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473753 | n.96A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473765 | n.108A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474153 | n.496C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474166 | n.509G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474349 | n.692A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474359 | n.702C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474406 | n.749T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474651 | n.995delT | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474662 | n.1005C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474777 | n.1120T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474896 | n.1239A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475011 | n.1354G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475089 | n.1432A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475115 | n.1458A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476015 | n.2358G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476708 | n.3051C>T | non_coding_transcript_exon_variant | 0.4 |
inhA | 1674252 | c.51C>T | synonymous_variant | 0.12 |
inhA | 1674365 | p.Pro55Arg | missense_variant | 0.25 |
inhA | 1674823 | p.Gly208Ser | missense_variant | 0.14 |
rpsA | 1833661 | p.Glu40Asp | missense_variant | 0.13 |
rpsA | 1833665 | p.Thr42Val | missense_variant | 0.13 |
rpsA | 1833673 | c.132C>G | synonymous_variant | 0.24 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.28 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.26 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.43 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.48 |
rpsA | 1833709 | c.168C>G | synonymous_variant | 0.6 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.66 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.64 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.64 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.64 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.61 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.59 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.59 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.46 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.44 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 0.44 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.46 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.46 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.35 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 0.33 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.34 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.36 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.37 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.37 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.31 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.31 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.29 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.18 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.17 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.32 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.32 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.39 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.4 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.39 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.43 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.44 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.49 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.5 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.43 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.43 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.48 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.49 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.53 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.51 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.6 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.57 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.49 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.48 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.46 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.49 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.29 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.29 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.29 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.38 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.4 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.4 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.47 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.5 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 0.61 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.61 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.61 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.56 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.55 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.54 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.55 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.55 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.52 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.4 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.28 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.27 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.26 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.28 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.29 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.29 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.37 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.41 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.43 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.4 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.26 |
rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.24 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.33 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.3 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.35 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 0.52 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.54 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.48 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.42 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.42 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.42 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.42 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.46 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.46 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.32 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.19 |
rpsA | 1834538 | p.Val333Met | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.95 |
ndh | 2102055 | p.Pro330Thr | missense_variant | 0.15 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288710 | p.Ala178Thr | missense_variant | 0.14 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086823 | p.Arg2Cys | missense_variant | 0.13 |
ald | 3087704 | c.885T>C | synonymous_variant | 0.15 |
ald | 3087713 | c.894G>C | synonymous_variant | 0.19 |
ald | 3087716 | c.897G>C | synonymous_variant | 0.19 |
ald | 3087727 | p.Ala303Gly | missense_variant | 0.21 |
ald | 3087729 | p.Ser304Ala | missense_variant | 0.21 |
ald | 3087737 | c.918G>C | synonymous_variant | 0.19 |
ald | 3087740 | p.Lys307Asn | missense_variant | 0.19 |
ald | 3087743 | c.924G>C | synonymous_variant | 0.2 |
ald | 3087746 | c.927G>C | synonymous_variant | 0.19 |
ald | 3087767 | c.948G>C | synonymous_variant | 0.15 |
ald | 3087771 | p.Met318Leu | missense_variant | 0.16 |
Rv3083 | 3448368 | c.-136C>T | upstream_gene_variant | 0.17 |
Rv3083 | 3449091 | p.Met196Ile | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474208 | c.206delA | frameshift_variant | 0.25 |
Rv3236c | 3612360 | p.Gly253Arg | missense_variant | 0.14 |
Rv3236c | 3612649 | c.468G>A | synonymous_variant | 0.33 |
alr | 3840627 | p.Ala265Asp | missense_variant | 0.12 |
alr | 3840688 | p.Asp245Asn | missense_variant | 0.11 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.24 |
rpoA | 3877926 | p.Leu194Val | missense_variant | 0.29 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.44 |
rpoA | 3877965 | c.543C>G | synonymous_variant | 0.4 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.42 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.42 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.32 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.32 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.3 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.36 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.23 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.23 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.14 |
clpC1 | 4038826 | p.Ile627Val | missense_variant | 0.31 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.29 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.29 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.35 |
clpC1 | 4038872 | c.1833C>G | synonymous_variant | 0.38 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.36 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.36 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.17 |
clpC1 | 4038905 | c.1800A>T | synonymous_variant | 0.2 |
clpC1 | 4038911 | c.1794G>C | synonymous_variant | 0.13 |
clpC1 | 4038983 | p.Asp574Glu | missense_variant | 0.15 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.15 |
clpC1 | 4039001 | p.Asn568Glu | missense_variant | 0.14 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.14 |
clpC1 | 4039034 | c.1671C>G | synonymous_variant | 0.14 |
clpC1 | 4039067 | p.Ser546Gly | missense_variant | 0.15 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.15 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.15 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.16 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.16 |
clpC1 | 4039094 | c.1611C>G | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.16 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.18 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.21 |
clpC1 | 4039121 | p.Val528Leu | missense_variant | 0.2 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.21 |
clpC1 | 4039382 | p.Ala441Ser | missense_variant | 0.21 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.19 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.2 |
clpC1 | 4039403 | p.Glu434Asp | missense_variant | 0.2 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.2 |
clpC1 | 4039412 | p.Ala431Val | missense_variant | 0.24 |
clpC1 | 4039416 | p.Glu430Ala | missense_variant | 0.27 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.42 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.47 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.47 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.48 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.46 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.46 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.45 |
clpC1 | 4039481 | p.Ala408Ser | missense_variant | 0.45 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.45 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.46 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.5 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.38 |
clpC1 | 4039532 | p.Asn391Ser | missense_variant | 0.17 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.42 |
clpC1 | 4039555 | c.1147_1149delGCG | conservative_inframe_deletion | 0.4 |
clpC1 | 4039565 | c.1139_1140insTCA | disruptive_inframe_insertion | 0.4 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.44 |
clpC1 | 4039575 | p.Ala377Glu | missense_variant | 0.38 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.38 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.4 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.4 |
clpC1 | 4039592 | c.1113G>T | synonymous_variant | 0.42 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.42 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.33 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.27 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.27 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.28 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.28 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.37 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.41 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.43 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.42 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.5 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.5 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.37 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.33 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.33 |
clpC1 | 4039943 | p.Ser254Ala | missense_variant | 0.36 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.34 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.33 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.32 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.43 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 0.51 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.5 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.34 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.34 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.38 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.36 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.4 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.45 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.41 |
clpC1 | 4040054 | c.651G>A | synonymous_variant | 0.31 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.31 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.45 |
clpC1 | 4040084 | c.621C>T | synonymous_variant | 0.37 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.45 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.41 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.37 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.44 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.44 |
clpC1 | 4040257 | p.Ala150Thr | missense_variant | 0.24 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.37 |
clpC1 | 4040300 | c.405C>G | synonymous_variant | 0.42 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.4 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.41 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.41 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.4 |
clpC1 | 4040318 | c.387C>T | synonymous_variant | 0.41 |
clpC1 | 4040336 | c.369G>C | synonymous_variant | 0.47 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.31 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.24 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.26 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.23 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.23 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.2 |
clpC1 | 4040648 | c.57G>A | synonymous_variant | 0.19 |
clpC1 | 4040669 | c.36C>T | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245786 | p.Ala852Thr | missense_variant | 1.0 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.13 |
embB | 4246235 | c.-279G>A | upstream_gene_variant | 0.13 |
embB | 4246256 | c.-258G>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |