Run ID: SRR6832659
Sample name:
Date: 04-04-2023 17:33:47
Number of reads: 2724877
Percentage reads mapped: 93.15
Strain: lineage4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.5 | streptomycin |
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 |
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 | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472222 | n.377G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472229 | n.384C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.33 |
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 | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.97 |
PPE35 | 2170419 | p.Met65Thr | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
ddn | 3987233 | c.390C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |