Run ID: ERR4407476
Sample name:
Date: 01-04-2023 05:45:41
Number of reads: 274613
Percentage reads mapped: 99.55
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 | 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 |
ccsA | 620444 | p.Val185Glu | missense_variant | 0.18 |
rpoB | 763245 | p.Glu1147* | stop_gained | 0.12 |
rpoC | 763328 | c.-42_-41insT | upstream_gene_variant | 1.0 |
rpoC | 764081 | p.Glu238Lys | missense_variant | 0.12 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776407 | p.Pro692Ala | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406254 | p.Gly363Ser | missense_variant | 0.12 |
Rv1258c | 1407421 | c.-81A>G | upstream_gene_variant | 0.2 |
embR | 1417076 | c.270_271delAC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473608 | n.-50G>A | upstream_gene_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917885 | c.-55G>A | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170606 | p.Tyr3His | missense_variant | 0.29 |
Rv1979c | 2221948 | p.Ala406Asp | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518197 | p.Asp28Ala | missense_variant | 0.29 |
kasA | 2518200 | p.Ile29Asn | missense_variant | 0.29 |
kasA | 2518201 | c.88delG | frameshift_variant | 0.29 |
kasA | 2518218 | p.Gly35Ala | missense_variant | 0.15 |
kasA | 2518226 | p.Ala38Ser | missense_variant | 0.15 |
pepQ | 2859886 | p.Ala178Asp | missense_variant | 0.12 |
ald | 3087095 | c.276C>T | synonymous_variant | 1.0 |
fbiB | 3641614 | c.83_108delATCTGAGCGCCGCCGTCGCCGCGGCG | frameshift_variant | 0.17 |
rpoA | 3877842 | c.666A>G | synonymous_variant | 0.12 |
ddn | 3987103 | p.Met87Thr | missense_variant | 0.11 |
clpC1 | 4038324 | p.Val794Ala | missense_variant | 0.13 |
panD | 4044122 | p.Arg54* | stop_gained | 0.25 |
embC | 4240974 | p.Val371Ala | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243405 | c.175_176delAC | frameshift_variant | 0.2 |
embB | 4249042 | c.2531delT | frameshift_variant | 0.12 |
ubiA | 4269990 | c.-157G>T | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |