Run ID: ERR2652975
Sample name:
Date: 31-03-2023 22:25:37
Number of reads: 851862
Percentage reads mapped: 99.72
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 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 |
mshA | 576562 | c.1215G>A | synonymous_variant | 0.11 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.11 |
rpoC | 766676 | p.Asp1103Asn | missense_variant | 0.12 |
mmpL5 | 777743 | c.736_737dupGG | frameshift_variant | 0.12 |
mmpR5 | 779069 | p.Phe27Ser | missense_variant | 0.1 |
fbiC | 1303643 | p.Pro238Leu | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673537 | p.Gln33Arg | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154296 | p.Ala606Thr | missense_variant | 0.1 |
katG | 2155608 | c.504C>A | synonymous_variant | 0.11 |
PPE35 | 2168914 | p.Pro567Ser | missense_variant | 0.17 |
Rv1979c | 2223029 | p.Phe46Leu | missense_variant | 0.13 |
pncA | 2289530 | c.-289T>C | upstream_gene_variant | 0.11 |
kasA | 2519361 | p.Tyr416Cys | missense_variant | 0.3 |
pepQ | 2859466 | p.Ala318Val | missense_variant | 0.14 |
Rv2752c | 3064999 | p.Gly398Glu | missense_variant | 0.11 |
Rv3083 | 3448664 | p.Arg54Leu | missense_variant | 0.13 |
fprA | 3474142 | c.141delG | frameshift_variant | 0.12 |
fprA | 3475112 | p.Gly369Val | missense_variant | 0.12 |
fbiA | 3640709 | p.Leu56Gln | missense_variant | 0.14 |
fbiA | 3641165 | p.Ile208Thr | missense_variant | 0.14 |
fbiA | 3641167 | p.Ile209Val | missense_variant | 0.12 |
fbiA | 3641315 | c.774delG | frameshift_variant | 0.12 |
fbiB | 3642641 | c.1107G>A | synonymous_variant | 0.13 |
alr | 3840232 | p.Arg397Cys | missense_variant | 0.15 |
clpC1 | 4038179 | c.2526C>T | synonymous_variant | 0.15 |
panD | 4044351 | c.-70T>C | upstream_gene_variant | 0.11 |
embC | 4240860 | p.Leu333Arg | missense_variant | 1.0 |
embA | 4242619 | c.-614C>T | upstream_gene_variant | 0.11 |
embC | 4242710 | p.Gln950Lys | missense_variant | 0.11 |
embA | 4246208 | c.2980delT | frameshift_variant | 0.11 |
embB | 4246448 | c.-66C>T | upstream_gene_variant | 0.12 |
embB | 4247084 | p.Asp191Asn | missense_variant | 0.11 |
embB | 4247096 | p.Pro195Ser | missense_variant | 0.12 |
embB | 4248526 | c.2018delT | frameshift_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338654 | c.-133A>G | upstream_gene_variant | 0.13 |
gid | 4408240 | c.-38A>G | upstream_gene_variant | 0.11 |