Run ID: ERR4024812
Sample name:
Date: 01-04-2023 04:09:43
Number of reads: 1680973
Percentage reads mapped: 80.37
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.96 |
lineage4.1.2 | Euro-American | T;H | None | 0.97 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.34 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9470 | c.2169G>A | synonymous_variant | 0.38 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.98 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.36 |
rpoB | 760106 | c.300G>A | synonymous_variant | 0.33 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.97 |
rpoC | 764263 | c.894G>A | synonymous_variant | 0.64 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.97 |
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 | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472669 | n.824_825insTAG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472677 | n.832C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472679 | n.834_835insAC | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472684 | n.841_846delGATCCG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472953 | n.1109_1112delTCTC | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472959 | n.1114_1115insTTTA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472975 | n.1130T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472991 | n.1146G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472992 | n.1147A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473020 | n.1175T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.93 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.97 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
fbiB | 3641454 | c.-81G>A | upstream_gene_variant | 0.38 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.92 |
embB | 4248705 | p.Pro731Leu | missense_variant | 0.66 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |