Run ID: ERR2229147
Sample name:
Date: 31-03-2023 16:44:34
Number of reads: 574625
Percentage reads mapped: 90.79
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7424 | c.123G>A | synonymous_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576697 | c.1350C>T | synonymous_variant | 0.22 |
ccsA | 620631 | c.741T>A | synonymous_variant | 0.12 |
rpoB | 761697 | p.Asp631Tyr | missense_variant | 0.17 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.15 |
rpoB | 762236 | c.2430G>T | synonymous_variant | 0.15 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 0.15 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.14 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.12 |
rpoC | 762899 | c.-471G>T | upstream_gene_variant | 0.13 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.15 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.29 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.26 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.35 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.35 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.27 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.14 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775857 | p.Gly875Val | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781679 | c.120C>G | synonymous_variant | 0.12 |
rpsL | 781682 | c.123T>G | synonymous_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305455 | p.Arg842Leu | missense_variant | 0.17 |
embR | 1417382 | c.-35G>A | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472522 | n.677T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472585 | n.740A>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474166 | n.509G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474167 | n.510T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474287 | n.631_649delCCTTTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474467 | n.810A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474799 | n.1143delT | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474803 | n.1146_1147insA | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475991 | n.2334T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475996 | n.2339T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476288 | n.2635_2643delGCACCCCCG | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476301 | n.2644_2645insCGGTGGCTT | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476316 | n.2659G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476546 | n.2889C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834123 | c.582C>T | synonymous_variant | 0.13 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.29 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.31 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.31 |
rpsA | 1834492 | c.951C>T | synonymous_variant | 0.31 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.17 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.17 |
rpsA | 1834508 | p.Ile323Val | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918579 | p.Arg214Trp | missense_variant | 0.12 |
ndh | 2102599 | c.444T>C | synonymous_variant | 0.15 |
ndh | 2102604 | c.439T>C | synonymous_variant | 0.15 |
ndh | 2102610 | c.433T>C | synonymous_variant | 0.17 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.14 |
ndh | 2103095 | c.-53T>A | upstream_gene_variant | 0.29 |
katG | 2155251 | c.861A>G | synonymous_variant | 0.15 |
katG | 2155862 | p.Met84Leu | missense_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168990 | c.1623T>C | synonymous_variant | 0.15 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.16 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.17 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.17 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.28 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.32 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.19 |
Rv1979c | 2222551 | p.Tyr205Phe | missense_variant | 0.12 |
Rv1979c | 2222575 | p.Trp197Leu | missense_variant | 0.15 |
Rv1979c | 2223283 | c.-119G>A | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290038 | c.-797G>A | upstream_gene_variant | 0.13 |
kasA | 2518645 | c.531G>T | synonymous_variant | 0.15 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.29 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.29 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.29 |
eis | 2714563 | p.Ile257Asn | missense_variant | 0.17 |
pepQ | 2860107 | c.312G>A | synonymous_variant | 0.17 |
pepQ | 2860597 | c.-179A>C | upstream_gene_variant | 0.18 |
ribD | 2987291 | p.Asp151Glu | missense_variant | 0.18 |
thyX | 3068108 | c.-163G>A | upstream_gene_variant | 0.2 |
thyA | 3074022 | p.Phe150Leu | missense_variant | 0.15 |
thyA | 3074188 | p.Gly95Asp | missense_variant | 0.12 |
ald | 3087918 | p.Ala367Ser | missense_variant | 0.33 |
fprA | 3475361 | p.Arg452Gln | missense_variant | 0.13 |
Rv3236c | 3613002 | p.Ala39Ser | missense_variant | 0.14 |
fbiA | 3641370 | c.830delG | frameshift_variant | 0.14 |
alr | 3840395 | p.Cys342* | stop_gained | 0.17 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
clpC1 | 4038691 | p.Asp672Asn | missense_variant | 0.12 |
embC | 4241865 | p.Leu668Pro | missense_variant | 0.18 |
embC | 4242195 | p.Gly778Val | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246395 | p.Gly1055* | stop_gained | 0.11 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |