Run ID: ERR4816133
Sample name:
Date: 01-04-2023 14:15:23
Number of reads: 1074572
Percentage reads mapped: 80.22
Strain: La1.8.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.2 | M.bovis | None | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.65 | streptomycin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7162 | c.-140C>T | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Gly | missense_variant | 1.0 |
rpoB | 759950 | c.144T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.14 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.26 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.31 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.12 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.24 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.28 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.19 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.21 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.15 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.12 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.12 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.12 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.13 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.13 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.12 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.13 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.13 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.14 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.14 |
rpoC | 764559 | p.Arg397His | missense_variant | 0.18 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.12 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.11 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.11 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.11 |
rpoC | 765838 | c.2469G>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
embR | 1416695 | p.Ser218Tyr | missense_variant | 1.0 |
atpE | 1461173 | c.129C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472274 | n.429A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.23 |
rrl | 1473425 | n.-233G>A | upstream_gene_variant | 0.12 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.12 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.12 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.12 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.22 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.21 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.29 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.25 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.25 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.21 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.25 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.33 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.33 |
rpsA | 1833775 | p.Glu78Asp | missense_variant | 0.29 |
rpsA | 1834099 | c.558C>T | synonymous_variant | 0.11 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.12 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.22 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.26 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.27 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.35 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.35 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.17 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.14 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.14 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.14 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.13 |
rpsA | 1834795 | c.1254C>T | synonymous_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103058 | c.-16T>C | upstream_gene_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2153966 | p.Ala716Ser | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168374 | p.Pro747Ser | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222511 | c.654C>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
folC | 2747631 | c.-33C>T | upstream_gene_variant | 1.0 |
Rv2752c | 3066302 | c.-111C>T | upstream_gene_variant | 0.12 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
ald | 3087871 | p.Leu351Arg | missense_variant | 0.11 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612811 | c.306G>A | synonymous_variant | 0.11 |
fbiB | 3641710 | p.Arg59Leu | missense_variant | 0.12 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039639 | p.Ile356Val | missense_variant | 0.11 |
clpC1 | 4039644 | p.His354Pro | missense_variant | 0.12 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242770 | p.Thr970Pro | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 0.94 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248372 | p.Arg620Pro | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
eis | 2714045 | c.1204_*78delNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNC | stop_lost&conservative_inframe_deletion&splice_region_variant | 1.0 |