Run ID: ERR4815528
Sample name:
Date: 01-04-2023 13:54:54
Number of reads: 385727
Percentage reads mapped: 75.06
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 | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.71 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6105 | p.Ile289Thr | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576390 | p.Val348Ala | missense_variant | 0.25 |
rpoC | 763655 | p.Glu96Arg | missense_variant | 0.13 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.12 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.12 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.12 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.17 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.17 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.18 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.17 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.17 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.18 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.17 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.17 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.18 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.2 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.2 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.2 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.18 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.17 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.14 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.14 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781672 | p.Tyr38Phe | missense_variant | 0.14 |
rplC | 800986 | p.Arg60Ser | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.15 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.43 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.43 |
alr | 3840310 | p.Arg371Trp | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.22 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.22 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.22 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |