Run ID: SRR13837760
Sample name:
Date: 03-04-2023 09:17:46
Number of reads: 147539
Percentage reads mapped: 96.42
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 | 5149 | c.-91G>C | upstream_gene_variant | 1.0 |
gyrB | 7090 | p.Asp617Glu | missense_variant | 1.0 |
gyrA | 8436 | p.Tyr379Asn | missense_variant | 1.0 |
fgd1 | 491701 | p.His307Asn | missense_variant | 1.0 |
ccsA | 619765 | c.-126G>A | upstream_gene_variant | 1.0 |
rpoC | 764443 | c.1074C>T | synonymous_variant | 0.33 |
mmpL5 | 775867 | p.Arg872Gly | missense_variant | 1.0 |
mmpL5 | 776710 | p.Cys591Ser | missense_variant | 1.0 |
mmpL5 | 777625 | p.Gln286Lys | missense_variant | 1.0 |
mmpS5 | 778811 | p.Phe32Ser | missense_variant | 1.0 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.2 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.2 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.22 |
embR | 1416901 | c.447G>C | synonymous_variant | 1.0 |
rrl | 1474466 | n.810delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475224 | n.1567T>C | non_coding_transcript_exon_variant | 1.0 |
PPE35 | 2170487 | c.126T>A | synonymous_variant | 1.0 |
Rv1979c | 2221853 | p.Phe438Ile | missense_variant | 1.0 |
ribD | 2987369 | c.531G>A | synonymous_variant | 1.0 |
thyA | 3073975 | p.Arg166Pro | missense_variant | 1.0 |
Rv3236c | 3612013 | c.1104A>T | synonymous_variant | 1.0 |
Rv3236c | 3612032 | p.Met362Arg | missense_variant | 1.0 |
embC | 4240425 | p.Arg188Pro | missense_variant | 1.0 |
embC | 4240477 | c.615C>A | synonymous_variant | 1.0 |
embA | 4244214 | p.Ala328Ser | missense_variant | 1.0 |
embA | 4244849 | c.1617C>G | synonymous_variant | 1.0 |
embB | 4247198 | p.Thr229Pro | missense_variant | 1.0 |
embB | 4247381 | p.Trp290Arg | missense_variant | 1.0 |
aftB | 4268115 | p.Leu241Arg | missense_variant | 1.0 |
aftB | 4268696 | c.141G>A | synonymous_variant | 1.0 |
ethA | 4326298 | c.1176G>A | synonymous_variant | 1.0 |
whiB6 | 4338567 | c.-46C>A | upstream_gene_variant | 1.0 |