Run ID: SRR6046096
Sample name:
Date: 04-04-2023 12:11:08
Number of reads: 377351
Percentage reads mapped: 56.23
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.44 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6904 | c.-398C>A | upstream_gene_variant | 0.17 |
gyrB | 6992 | p.Arg585Cys | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7702 | p.Leu134Pro | missense_variant | 0.25 |
gyrA | 7772 | c.471C>T | synonymous_variant | 0.2 |
gyrA | 9233 | c.1932C>T | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9536 | c.2235C>G | synonymous_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575241 | c.-107C>T | upstream_gene_variant | 0.29 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.22 |
rpoB | 759663 | c.-144G>A | upstream_gene_variant | 0.22 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761825 | p.Asn673Lys | missense_variant | 0.22 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.18 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.18 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.15 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.15 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.23 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.15 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.2 |
rpoC | 764737 | c.1368G>T | synonymous_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766516 | c.3147C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777878 | c.603C>T | synonymous_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781791 | p.Ser78Pro | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473726 | n.69C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474011 | n.354G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2107_2108delAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673250 | c.-189delT | upstream_gene_variant | 0.22 |
inhA | 1673787 | c.-415G>C | upstream_gene_variant | 0.17 |
rpsA | 1834579 | c.1038C>A | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101791 | p.Thr418Ala | missense_variant | 1.0 |
PPE35 | 2169128 | c.1484dupA | frameshift_variant | 1.0 |
Rv1979c | 2222797 | p.Pro123Leu | missense_variant | 0.13 |
Rv1979c | 2223237 | c.-73C>T | upstream_gene_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288966 | c.276G>A | synonymous_variant | 0.13 |
pncA | 2289999 | c.-758G>C | upstream_gene_variant | 0.2 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.27 |
Rv2752c | 3066078 | c.113delG | frameshift_variant | 0.11 |
thyX | 3067406 | c.540A>G | synonymous_variant | 0.18 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.22 |
Rv3083 | 3448817 | p.Asn105Thr | missense_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474204 | p.Gln66His | missense_variant | 0.25 |
Rv3236c | 3612331 | c.785delT | frameshift_variant | 0.13 |
ddn | 3986752 | c.-92C>T | upstream_gene_variant | 0.13 |
clpC1 | 4038394 | p.Arg771Ser | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.92 |
aftB | 4267514 | c.1323G>A | synonymous_variant | 0.17 |
aftB | 4268958 | c.-122A>G | upstream_gene_variant | 0.17 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.29 |
whiB6 | 4338480 | c.42T>G | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |