Run ID: ERR2229266
Sample name:
Date: 31-03-2023 16:54:03
Number of reads: 1130501
Percentage reads mapped: 99.21
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 |
fgd1 | 491457 | c.675C>A | synonymous_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.5 |
mshA | 576518 | p.Ser391Ala | missense_variant | 0.33 |
rpoC | 765302 | p.Glu645Gln | missense_variant | 0.11 |
rpoC | 766819 | p.His1150Gln | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.11 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.18 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_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 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167746 | p.Thr956Ser | missense_variant | 0.15 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169091 | p.Val508Leu | missense_variant | 0.26 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.12 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.19 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.12 |
PPE35 | 2169944 | c.669G>C | synonymous_variant | 0.12 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.26 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518791 | p.Ala226Val | missense_variant | 0.15 |
kasA | 2519099 | c.987delC | frameshift_variant | 0.13 |
pepQ | 2859818 | p.Ala201Ser | missense_variant | 0.14 |
fprA | 3474875 | p.Gly290Asp | missense_variant | 0.17 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.19 |
embC | 4241836 | c.1974A>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244666 | c.1434G>A | synonymous_variant | 0.12 |
embA | 4244814 | c.1582C>T | synonymous_variant | 0.25 |
embA | 4245390 | p.Lys720Glu | missense_variant | 0.2 |
embB | 4246553 | c.40C>A | synonymous_variant | 0.29 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |