Run ID: SRR8692882
Sample name:
Date: 13-08-2023 21:33:05
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 1.0 | linezolid |
katG | 2155786 | p.Ala109Val | missense_variant | 0.12 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5615 | p.Ser126Ala | missense_variant | 0.12 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.11 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.11 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.11 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.11 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.11 |
gyrA | 7404 | p.Val35Met | missense_variant | 0.17 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.12 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.12 |
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.13 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.11 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.16 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.11 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.14 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.13 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.15 |
gyrA | 8531 | c.1230G>C | synonymous_variant | 0.12 |
gyrA | 8536 | p.Glu412Ala | missense_variant | 0.11 |
gyrA | 8542 | p.Val414Ala | missense_variant | 0.1 |
gyrA | 8547 | p.Ile416Val | missense_variant | 0.11 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.11 |
gyrA | 8557 | p.Ala419Gly | missense_variant | 0.11 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.1 |
gyrA | 8567 | p.Ile422Met | missense_variant | 0.11 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.11 |
fgd1 | 491325 | c.543G>T | synonymous_variant | 0.14 |
fgd1 | 491335 | p.Ala185Ser | missense_variant | 0.14 |
mshA | 576459 | p.Ala371Val | missense_variant | 0.17 |
ccsA | 620795 | p.Ala302Asp | missense_variant | 0.13 |
rpoB | 759844 | p.Pro13His | missense_variant | 0.12 |
rpoB | 760331 | c.525G>T | synonymous_variant | 0.2 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.2 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.18 |
rpoB | 760353 | p.Glu183Ser | missense_variant | 0.18 |
rpoB | 760356 | p.Thr184Ser | missense_variant | 0.14 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.13 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.12 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.12 |
rpoB | 760380 | p.Thr192Asp | missense_variant | 0.12 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.14 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.13 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.13 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.13 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.19 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.21 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.2 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.18 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.18 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.18 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.18 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.16 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.16 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.11 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.12 |
rpoB | 761887 | p.Gln694Arg | missense_variant | 0.11 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.12 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.12 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.13 |
rpoC | 764346 | p.Pro326Gln | missense_variant | 0.13 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.15 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.11 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.11 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.11 |
rpoC | 765807 | p.Gln813Arg | missense_variant | 0.1 |
rpoC | 766055 | p.Gly896Cys | missense_variant | 0.12 |
rpoC | 766155 | p.Ala929Glu | missense_variant | 0.14 |
rpoC | 766344 | p.Gly992Val | missense_variant | 0.14 |
rpoC | 766351 | c.2982C>A | synonymous_variant | 0.13 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.1 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.12 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.12 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.12 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.14 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.17 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.22 |
rpoC | 766771 | c.3402G>C | synonymous_variant | 0.25 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.22 |
rpoC | 766775 | p.Arg1136Lys | missense_variant | 0.22 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.22 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766807 | c.3438T>C | synonymous_variant | 0.22 |
rpoC | 766840 | c.3471C>A | synonymous_variant | 0.25 |
mmpL5 | 775749 | p.Gly911Val | missense_variant | 0.14 |
mmpL5 | 776527 | p.Met652Val | missense_variant | 0.11 |
rpsL | 781640 | p.Ser27Arg | missense_variant | 0.11 |
rpsL | 781673 | p.Tyr38* | stop_gained | 0.15 |
rplC | 801333 | c.525G>T | synonymous_variant | 0.22 |
fbiC | 1304103 | c.1173G>T | synonymous_variant | 0.12 |
fbiC | 1305408 | c.2478G>T | synonymous_variant | 0.25 |
Rv1258c | 1406421 | p.Phe307Ser | missense_variant | 0.12 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 1.0 |
Rv1258c | 1407050 | c.291C>A | synonymous_variant | 0.2 |
embR | 1416424 | c.924C>A | synonymous_variant | 0.14 |
embR | 1417238 | p.Ala37Asp | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471973 | n.128C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472866 | n.1021C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474034 | n.377G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474518 | n.861C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474669 | n.1012G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474749 | n.1092C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476404 | n.2747G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476430 | n.2773G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476439 | n.2782G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1674076 | p.Thr213Ala | missense_variant | 0.11 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.19 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.18 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.17 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.17 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.15 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.14 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.14 |
rpsA | 1833727 | c.186G>A | synonymous_variant | 0.17 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.17 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.19 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.18 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.14 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.13 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.12 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.11 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.11 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.14 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.14 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.14 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.15 |
rpsA | 1834705 | c.1164C>G | synonymous_variant | 0.15 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.12 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.12 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.14 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.14 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.14 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.14 |
ndh | 2102464 | c.579C>T | synonymous_variant | 0.2 |
PPE35 | 2170339 | p.Val92Leu | missense_variant | 0.15 |
kasA | 2518618 | c.504G>T | synonymous_variant | 0.17 |
kasA | 2518720 | c.606C>A | synonymous_variant | 0.17 |
kasA | 2518735 | c.621C>A | synonymous_variant | 0.15 |
kasA | 2518746 | p.Ser211Tyr | missense_variant | 0.15 |
kasA | 2518769 | p.Arg219Ser | missense_variant | 0.15 |
folC | 2746265 | p.Ser445* | stop_gained | 0.13 |
folC | 2746590 | p.Gly337Cys | missense_variant | 0.15 |
pepQ | 2859746 | p.Leu225Met | missense_variant | 0.12 |
thyX | 3067265 | p.Phe227Leu | missense_variant | 0.13 |
fprA | 3474083 | p.Ala26Asp | missense_variant | 0.21 |
fprA | 3475173 | c.1169delA | frameshift_variant | 0.17 |
fprA | 3475272 | p.His422Gln | missense_variant | 0.15 |
whiB7 | 3568771 | c.-92C>A | upstream_gene_variant | 0.15 |
whiB7 | 3568875 | c.-196C>A | upstream_gene_variant | 0.12 |
fbiA | 3640679 | p.Asn46Ser | missense_variant | 0.12 |
fbiB | 3641310 | c.-225C>A | upstream_gene_variant | 0.14 |
alr | 3840629 | c.792C>G | synonymous_variant | 0.11 |
rpoA | 3877591 | p.Leu306Pro | missense_variant | 0.12 |
clpC1 | 4038180 | p.Gly842Val | missense_variant | 0.17 |
clpC1 | 4038185 | c.2520G>T | synonymous_variant | 0.17 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.14 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.17 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.18 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.17 |
clpC1 | 4039100 | c.1605C>A | synonymous_variant | 0.13 |
clpC1 | 4039268 | c.1437C>T | synonymous_variant | 0.13 |
clpC1 | 4039356 | p.Leu450Pro | missense_variant | 0.12 |
clpC1 | 4040065 | p.Leu214Met | missense_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.12 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.12 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.12 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.13 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.13 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.12 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.12 |
clpC1 | 4040175 | p.Asn177Ile | missense_variant | 0.12 |
clpC1 | 4040195 | c.510G>C | synonymous_variant | 0.13 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.12 |
clpC1 | 4040201 | c.504C>A | synonymous_variant | 0.12 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.12 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.12 |
clpC1 | 4040213 | p.Ser164Tyr | missense_variant | 0.12 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.14 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.15 |
embC | 4239736 | c.-127C>A | upstream_gene_variant | 0.12 |
embC | 4242368 | p.Arg836Ser | missense_variant | 0.15 |
embC | 4242987 | p.Ala1042Glu | missense_variant | 0.12 |
embA | 4244201 | p.Trp323Cys | missense_variant | 0.12 |
embA | 4244317 | p.Phe362Ser | missense_variant | 0.11 |
embA | 4245977 | p.Asp915Glu | missense_variant | 0.15 |
embB | 4246760 | p.Val83Met | missense_variant | 0.12 |
embB | 4248542 | p.Ala677Ser | missense_variant | 0.14 |
embB | 4248934 | p.Asn807Lys | missense_variant | 0.17 |
aftB | 4267168 | p.Gln557Lys | missense_variant | 0.13 |
ubiA | 4269273 | p.Met187Ile | missense_variant | 0.12 |
ethA | 4326159 | p.Val439Leu | missense_variant | 0.13 |
ethA | 4326732 | p.Ala248Ser | missense_variant | 0.14 |
ethR | 4326742 | c.-807C>A | upstream_gene_variant | 0.13 |
ethR | 4326838 | c.-711G>T | upstream_gene_variant | 0.13 |
ethR | 4327441 | c.-108G>T | upstream_gene_variant | 0.17 |
ethR | 4327989 | c.442delT | frameshift_variant | 0.13 |
ethA | 4328061 | c.-588C>A | upstream_gene_variant | 0.22 |
ethR | 4328111 | p.Ala188Val | missense_variant | 0.29 |
gid | 4408153 | p.Gly17Val | missense_variant | 0.15 |