Run ID: ERR144557
Sample name:
Date: 31-03-2023 14:05:33
Number of reads: 10184195
Percentage reads mapped: 89.92
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472222 | n.377G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472229 | n.384C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474816 | n.1159G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474830 | n.1173A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.98 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.28 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.25 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.24 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 0.64 |
fbiB | 3641578 | p.Leu15Arg | missense_variant | 0.97 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.24 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.2 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.99 |
embA | 4244510 | c.1278G>A | synonymous_variant | 0.95 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |