Run ID: ERR2514345
Sample name:
Date: 31-03-2023 20:16:50
Number of reads: 1573700
Percentage reads mapped: 94.25
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.58 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.24 |
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 | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475900 | n.2243A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475938 | n.2281C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475954 | n.2297A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.36 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.26 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |