Run ID: SRR6824423
Sample name:
Date: 04-04-2023 16:35:39
Number of reads: 8541622
Percentage reads mapped: 84.42
Strain: lineage4.4.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.2 | Euro-American | T1;T2 | None | 1.0 |
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 |
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 | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472149 | n.304G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472974 | n.1129A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472975 | n.1130T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1834168 | c.627C>T | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155080 | c.1032G>A | synonymous_variant | 1.0 |
PPE35 | 2168863 | c.1750C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |