Run ID: SRR13837699
Sample name:
Date: 03-04-2023 09:16:10
Number of reads: 295602
Percentage reads mapped: 95.58
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 | 6027 | p.His263Arg | missense_variant | 1.0 |
mshA | 576327 | p.Phe327Tyr | missense_variant | 1.0 |
rpoB | 759707 | c.-100C>T | upstream_gene_variant | 1.0 |
rpoB | 760178 | c.372G>C | synonymous_variant | 1.0 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.18 |
rpoB | 762284 | c.2478G>A | synonymous_variant | 1.0 |
rpoC | 764262 | p.Val298Ala | missense_variant | 1.0 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.11 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.11 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.12 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.12 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.14 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.14 |
mmpL5 | 777280 | p.Ala401Ser | missense_variant | 1.0 |
mmpS5 | 778853 | p.Val18Ala | missense_variant | 1.0 |
embR | 1416662 | p.Arg229Pro | missense_variant | 1.0 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476682 | n.3025C>T | non_coding_transcript_exon_variant | 0.2 |
katG | 2155675 | p.Arg146Leu | missense_variant | 1.0 |
Rv1979c | 2222433 | c.732A>G | synonymous_variant | 1.0 |
ald | 3086631 | c.-189A>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612954 | c.162delC | frameshift_variant | 1.0 |
alr | 3840284 | p.Trp379* | stop_gained | 1.0 |
embC | 4240042 | p.Asn60Lys | missense_variant | 1.0 |
embB | 4245806 | c.-708G>A | upstream_gene_variant | 0.93 |
embB | 4247075 | c.563dupT | frameshift_variant | 1.0 |
embB | 4247839 | c.1326G>A | synonymous_variant | 1.0 |
embB | 4249763 | p.Thr1084Pro | missense_variant | 1.0 |
ethA | 4326860 | p.Leu205Pro | missense_variant | 1.0 |