Run ID: SRR13837600
Sample name:
Date: 03-04-2023 09:14:20
Number of reads: 2938966
Percentage reads mapped: 95.03
Strain: lineage4.9
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2155185 | c.926_927insA | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8396 | p.Tyr365* | stop_gained | 1.0 |
fgd1 | 490821 | p.Glu13Asp | missense_variant | 1.0 |
mshA | 575959 | p.Gln204His | missense_variant | 1.0 |
rpoC | 766364 | p.Ala999Ser | missense_variant | 1.0 |
mmpL5 | 775945 | p.Val846Leu | missense_variant | 1.0 |
mmpL5 | 778345 | p.Leu46Ile | missense_variant | 1.0 |
mmpL5 | 778992 | c.-512C>T | upstream_gene_variant | 1.0 |
mmpR5 | 779231 | p.Glu81Val | missense_variant | 1.0 |
fbiC | 1303186 | p.Tyr86His | missense_variant | 1.0 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673157 | c.-283G>C | upstream_gene_variant | 0.99 |
ndh | 2101749 | p.Thr432Ser | missense_variant | 0.99 |
katG | 2155982 | p.Asn44His | missense_variant | 1.0 |
PPE35 | 2168042 | c.2571G>C | synonymous_variant | 1.0 |
PPE35 | 2169365 | c.1248C>T | synonymous_variant | 1.0 |
thyX | 3067878 | p.Val23Gly | missense_variant | 1.0 |
fbiD | 3339188 | p.Thr24Ser | missense_variant | 1.0 |
fprA | 3474999 | c.993G>T | synonymous_variant | 1.0 |
whiB7 | 3568496 | p.Pro62Ser | missense_variant | 1.0 |
Rv3236c | 3612323 | p.Pro265Gln | missense_variant | 1.0 |
fbiB | 3641121 | c.-414C>A | upstream_gene_variant | 1.0 |
clpC1 | 4038346 | p.Glu787* | stop_gained | 1.0 |
embC | 4239894 | p.Ala11Gly | missense_variant | 1.0 |
ethA | 4327073 | p.Leu134Pro | missense_variant | 1.0 |