Run ID: ERR2514479
Sample name:
Date: 31-03-2023 20:21:48
Number of reads: 1458976
Percentage reads mapped: 99.28
Strain: lineage4.8.2
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 |
lineage4.8.2 | 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 | 0.4 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8135 | c.834C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776891 | p.Gln530His | 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 | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.38 |
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 | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473792 | n.135C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.24 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.12 |
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 | 3448508 | c.6_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |