Run ID: SRR14782595
Sample name:
Date: 03-04-2023 11:31:49
Number of reads: 2203006
Percentage reads mapped: 99.62
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.25 |
fgd1 | 491424 | c.650_655delCCGCTG | disruptive_inframe_deletion | 1.0 |
mshA | 575915 | p.Asp190Asn | missense_variant | 0.99 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.17 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.32 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.17 |
mshA | 576479 | p.Pro378Ala | missense_variant | 0.15 |
mshA | 576616 | c.1269G>C | synonymous_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 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.96 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.19 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.15 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.24 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.62 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.19 |
Rv3083 | 3448322 | c.-182G>A | upstream_gene_variant | 0.98 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 0.67 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.17 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.28 |
rpoA | 3878590 | c.-83G>C | upstream_gene_variant | 0.33 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.5 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.8 |
embC | 4240373 | c.511C>T | synonymous_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.43 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.35 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.2 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.2 |
embB | 4246904 | p.Val131Met | missense_variant | 1.0 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.18 |
whiB6 | 4338205 | p.Val106Gly | missense_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |