Run ID: ERR11050087
Sample name:
Date: 02-04-2023 11:04:25
Number of reads: 3769352
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 | 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 | 9647 | c.2346C>G | synonymous_variant | 0.26 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.42 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.25 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.36 |
mshA | 576606 | p.Ala420Gly | missense_variant | 0.24 |
mshA | 576609 | p.Ala421Gly | missense_variant | 0.24 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.43 |
mshA | 576618 | p.His424Pro | missense_variant | 0.25 |
rpoB | 760975 | p.Met390Thr | missense_variant | 0.99 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.27 |
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 | 1.0 |
rrl | 1475090 | n.1433A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.38 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.14 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170035 | p.Val193Gly | missense_variant | 0.2 |
PPE35 | 2170041 | p.Thr191Arg | missense_variant | 0.24 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.27 |
pepQ | 2859933 | c.486C>G | synonymous_variant | 0.18 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.19 |
ribD | 2987498 | c.660C>G | synonymous_variant | 0.19 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.17 |
Rv2752c | 3065602 | p.Asp197Gly | missense_variant | 0.27 |
thyX | 3067944 | p.Val1Gly | missense_variant | 0.22 |
ald | 3086767 | c.-53A>C | upstream_gene_variant | 1.0 |
ald | 3087816 | p.Cys333Gly | missense_variant | 0.19 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.25 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.33 |
rpoA | 3878580 | c.-73A>C | upstream_gene_variant | 0.33 |
rpoA | 3878587 | c.-80T>A | upstream_gene_variant | 0.29 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.77 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.35 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243682 | c.450T>G | synonymous_variant | 0.29 |
embA | 4244990 | c.1758G>C | synonymous_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.28 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.28 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.33 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.14 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.32 |
aftB | 4267715 | c.1122G>A | synonymous_variant | 0.97 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |