Run ID: ERR2652962
Sample name:
Date: 31-03-2023 22:25:16
Number of reads: 592566
Percentage reads mapped: 99.74
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 |
---|---|---|---|---|
gyrB | 5487 | p.Gly83Asp | missense_variant | 0.13 |
gyrB | 5739 | p.Thr167Met | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9814 | p.Asn838Ser | missense_variant | 0.12 |
mshA | 575424 | p.Arg26His | missense_variant | 0.11 |
rpoB | 762334 | p.Gly843Asp | missense_variant | 0.13 |
rpoC | 763917 | p.Glu183Gly | missense_variant | 0.22 |
rpoC | 766826 | p.His1153Tyr | missense_variant | 0.12 |
mmpR5 | 779471 | p.Thr161Ile | missense_variant | 0.12 |
rplC | 801349 | c.541T>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673431 | c.-771G>A | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102656 | c.387C>T | synonymous_variant | 0.11 |
PPE35 | 2169722 | c.891C>T | synonymous_variant | 0.14 |
pncA | 2290211 | c.-970G>A | upstream_gene_variant | 0.14 |
kasA | 2518018 | c.-97A>T | upstream_gene_variant | 0.11 |
kasA | 2518331 | c.218_219delGC | frameshift_variant | 0.14 |
kasA | 2518697 | p.Cys195Arg | missense_variant | 0.12 |
folC | 2746834 | c.764delC | frameshift_variant | 0.13 |
Rv2752c | 3065955 | p.Leu79Phe | missense_variant | 0.11 |
thyX | 3067344 | p.Ser201Asn | missense_variant | 0.17 |
fprA | 3474327 | c.321G>A | synonymous_variant | 0.11 |
fprA | 3474751 | p.Ile249Phe | missense_variant | 0.14 |
Rv3236c | 3612515 | p.Arg201His | missense_variant | 0.15 |
fbiB | 3642178 | c.646delG | frameshift_variant | 0.11 |
embC | 4240860 | p.Leu333Arg | missense_variant | 1.0 |
embA | 4244337 | c.1105C>T | synonymous_variant | 0.14 |
embA | 4244407 | p.Thr392Met | missense_variant | 0.13 |
embB | 4247377 | c.864G>A | synonymous_variant | 0.12 |
embB | 4248353 | p.Val614Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |