Run ID: SRR6046710
Sample name:
Date: 04-04-2023 12:21:58
Number of reads: 1094666
Percentage reads mapped: 84.41
Strain: lineage4.8.2
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 |
lineage4.8.2 | 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 | 0.89 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7740 | p.Glu147Lys | missense_variant | 0.12 |
gyrA | 8135 | c.834C>T | synonymous_variant | 1.0 |
mshA | 576490 | c.1143G>C | synonymous_variant | 0.17 |
ccsA | 619715 | c.-176C>T | upstream_gene_variant | 0.12 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776891 | p.Gln530His | 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 | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.38 |
tlyA | 1917783 | c.-157G>T | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859690 | c.729C>T | synonymous_variant | 0.13 |
Rv3236c | 3612878 | p.Thr80Asn | missense_variant | 0.12 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244774 | c.1542G>A | synonymous_variant | 0.18 |
embB | 4247656 | p.Lys381Asn | missense_variant | 0.14 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.19 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |