Run ID: ERR2515055
Sample name:
Date: 17-08-2022 18:34:01
Number of reads: 680799
Percentage reads mapped: 83.3
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.22 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6610 | c.-692C>T | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9390 | p.Thr697Ala | missense_variant | 1.0 |
gyrA | 9556 | p.Thr752Lys | missense_variant | 0.11 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.1 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.1 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.11 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.12 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.11 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.11 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.11 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.11 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.12 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.11 |
rpoB | 762177 | p.Arg791Ser | missense_variant | 0.12 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.15 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762612 | p.Ser936Arg | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.1 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.1 |
rpoC | 764517 | p.Asp383Gly | missense_variant | 0.15 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.18 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.2 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.13 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.12 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303151 | p.Gly74Ala | missense_variant | 0.13 |
embR | 1416196 | c.1152G>A | synonymous_variant | 0.18 |
embR | 1416225 | p.Glu375Gln | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471981 | n.136C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473293 | n.1449A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475731 | n.2074G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475760 | n.2103C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.6 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.11 |
rpsA | 1833727 | c.186G>T | synonymous_variant | 0.11 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.12 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.12 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.12 |
rpsA | 1833757 | c.216C>T | synonymous_variant | 0.11 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.11 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.19 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.23 |
rpsA | 1833976 | c.435C>G | synonymous_variant | 0.14 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.13 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.31 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.13 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.21 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.27 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.12 |
rpsA | 1834023 | c.482_483insC | frameshift_variant | 0.13 |
rpsA | 1834026 | c.486delG | frameshift_variant | 0.12 |
rpsA | 1834030 | c.489C>T | synonymous_variant | 0.12 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.12 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.12 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.25 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.12 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.12 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.12 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 0.11 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.1 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.11 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.14 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.13 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.13 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.13 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.13 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.12 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.12 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.14 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.15 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
eis | 2715130 | p.Arg68Leu | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.27 |
folC | 2747372 | p.Thr76Asn | missense_variant | 0.12 |
thyX | 3067244 | c.702C>A | synonymous_variant | 0.13 |
thyA | 3074036 | p.Cys146Ser | missense_variant | 0.12 |
thyA | 3074402 | p.Thr24Ala | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiB | 3641658 | p.Asp42His | missense_variant | 0.12 |
fbiB | 3641665 | p.Asp44Ala | missense_variant | 0.11 |
fbiB | 3641668 | p.Val45Ala | missense_variant | 0.11 |
fbiB | 3642627 | p.Arg365Cys | missense_variant | 0.12 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
alr | 3841503 | c.-83G>A | upstream_gene_variant | 0.12 |
embC | 4241118 | c.1257_1258insGGCAGC | conservative_inframe_insertion | 0.14 |
embC | 4242073 | c.2211C>T | synonymous_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethR | 4328102 | c.555_560delGTCATT | disruptive_inframe_deletion | 0.12 |
ethR | 4328111 | p.Ala188Gly | missense_variant | 0.12 |
ethR | 4328113 | c.565_566insAATGAC | stop_gained&disruptive_inframe_insertion | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |