Run ID: SRR9940986
Sample name:
Date: 04-04-2023 23:02:32
Number of reads: 1100372
Percentage reads mapped: 99.39
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 | 2154100 | p.Ser671* | stop_gained | 0.13 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
fgd1 | 491016 | c.234C>A | synonymous_variant | 0.14 |
fgd1 | 491574 | p.Asp264Glu | missense_variant | 0.22 |
mshA | 576544 | c.1197C>A | synonymous_variant | 0.2 |
rpoC | 764087 | p.Leu240Phe | missense_variant | 0.17 |
rpoC | 764618 | p.Leu417Val | missense_variant | 0.12 |
rpoC | 765026 | p.Ala553Ser | missense_variant | 0.12 |
rpsL | 781524 | c.-36C>A | upstream_gene_variant | 0.13 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474131 | n.474C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474282 | n.625G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474482 | n.825G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475425 | n.1768G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475564 | n.1907C>A | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673993 | p.Tyr185Cys | missense_variant | 0.18 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.26 |
ndh | 2102634 | p.Gly137Ser | missense_variant | 0.13 |
ndh | 2103040 | c.3G>T | start_lost | 0.14 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.29 |
katG | 2155067 | p.Gly349Cys | missense_variant | 0.15 |
PPE35 | 2168759 | c.1854C>G | synonymous_variant | 0.11 |
PPE35 | 2170598 | c.15G>A | synonymous_variant | 1.0 |
whiB7 | 3568501 | p.Ala60Asp | missense_variant | 0.11 |
alr | 3840612 | p.Gly270Val | missense_variant | 0.16 |
rpoA | 3878623 | c.-116C>A | upstream_gene_variant | 0.13 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.36 |
embC | 4240849 | c.987C>T | synonymous_variant | 0.13 |
embB | 4245650 | c.-864C>A | upstream_gene_variant | 0.12 |
embB | 4247208 | p.Ala232Glu | missense_variant | 0.13 |
embB | 4248884 | p.Asn791Asp | missense_variant | 0.13 |
aftB | 4268588 | c.249G>T | synonymous_variant | 0.22 |