Run ID: ERR2512986
Sample name:
Date: 31-03-2023 19:23:14
Number of reads: 2054432
Percentage reads mapped: 76.88
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.58 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575160 | c.-187delT | upstream_gene_variant | 0.12 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.14 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.12 |
rpoB | 761452 | p.Val549Ala | missense_variant | 0.12 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.1 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.12 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.15 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.2 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.19 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.21 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.19 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.21 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.21 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.24 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.27 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.25 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.25 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.23 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.23 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.22 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.21 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.23 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.17 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763397 | p.Leu10Ile | missense_variant | 0.11 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.16 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.14 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.14 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.13 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.12 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.12 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.11 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.15 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.15 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.15 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.16 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.16 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.21 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.21 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.21 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.22 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.2 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.18 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.13 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.11 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.12 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.13 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.13 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.13 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.12 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.12 |
rpoC | 764731 | c.1362G>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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.93 |
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 | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.57 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475768 | n.2112T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475768 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.38 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.1 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.18 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.19 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.2 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.2 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.19 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.17 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.15 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.12 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.11 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.14 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.17 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.13 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.17 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223117 | c.48C>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859846 | p.Glu191Asp | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4039547 | c.1131_1157delGGCGATGGTGGCCGCCGCGACCCTGGC | disruptive_inframe_deletion | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244350 | p.Leu373Pro | missense_variant | 1.0 |
embA | 4244800 | p.Val523Glu | missense_variant | 0.2 |
aftB | 4267146 | p.Ala564Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |