Run ID: ERR2660545
Sample name:
Date: 31-03-2023 22:55:06
Number of reads: 4992641
Percentage reads mapped: 88.84
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | 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 | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472669 | n.824_825insTAG | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472677 | n.832C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472679 | n.834_835insAC | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472684 | n.841_846delGATCCG | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475150 | n.1493C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 0.33 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |