Run ID: SRR9940975
Sample name:
Date: 04-04-2023 23:04:29
Number of reads: 750597
Percentage reads mapped: 99.9
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 | 5632 | c.393A>G | synonymous_variant | 0.11 |
gyrB | 6464 | p.Lys409Glu | missense_variant | 0.12 |
gyrB | 7127 | p.Val630Phe | missense_variant | 0.14 |
rpoB | 759819 | p.Arg5Ser | missense_variant | 0.15 |
rpoC | 765275 | c.1906C>A | synonymous_variant | 0.11 |
mmpL5 | 776778 | p.Arg568His | missense_variant | 0.11 |
mmpL5 | 777296 | c.1185C>T | synonymous_variant | 0.14 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472434 | n.589T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474773 | n.1116C>A | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.16 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.16 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.33 |
rpsA | 1834046 | p.Ile169Val | missense_variant | 0.12 |
ndh | 2102538 | p.Lys169Gln | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.53 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.53 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.25 |
PPE35 | 2170598 | c.15G>A | synonymous_variant | 1.0 |
kasA | 2519242 | c.1128C>A | synonymous_variant | 0.25 |
folC | 2746257 | p.Asp448His | missense_variant | 0.11 |
folC | 2747254 | c.345C>T | synonymous_variant | 0.12 |
Rv2752c | 3064855 | p.Lys446Arg | missense_variant | 0.12 |
Rv3236c | 3611992 | c.1125T>G | synonymous_variant | 0.25 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.67 |
clpC1 | 4040415 | p.Gln97Arg | missense_variant | 0.12 |
embC | 4240432 | c.570C>A | synonymous_variant | 0.11 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.42 |
embC | 4241756 | c.1894C>T | synonymous_variant | 0.15 |
embA | 4245391 | p.Lys720Met | missense_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.2 |
embB | 4248434 | c.1928_1930delCCA | disruptive_inframe_deletion | 0.12 |
aftB | 4267867 | p.Leu324Met | missense_variant | 0.18 |