Run ID: SRR13837916
Sample name:
Date: 03-04-2023 09:21:59
Number of reads: 1488242
Percentage reads mapped: 97.25
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 | 5760 | p.Trp174Leu | missense_variant | 1.0 |
gyrB | 6662 | p.Phe475Val | missense_variant | 1.0 |
rpoB | 760087 | p.Ser94Phe | missense_variant | 0.98 |
rpoC | 766854 | p.Leu1162Gln | missense_variant | 0.97 |
mmpL5 | 778416 | p.Pro22Leu | missense_variant | 1.0 |
rplC | 801126 | c.318C>T | synonymous_variant | 0.98 |
rrl | 1475354 | n.1697A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674867 | p.Trp222Cys | missense_variant | 0.98 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.13 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.12 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.12 |
katG | 2154601 | p.Gly504Val | missense_variant | 1.0 |
Rv1979c | 2222910 | c.255A>G | synonymous_variant | 1.0 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.12 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.11 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.12 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.12 |
pepQ | 2859714 | c.705C>A | synonymous_variant | 1.0 |
ald | 3087172 | p.Glu118Ala | missense_variant | 1.0 |
ald | 3087905 | c.1086G>A | synonymous_variant | 1.0 |
fprA | 3475069 | c.1064dupA | frameshift_variant&stop_gained | 0.97 |
Rv3236c | 3613280 | c.-164G>C | upstream_gene_variant | 1.0 |
alr | 3841499 | c.-79C>T | upstream_gene_variant | 1.0 |
rpoA | 3878156 | p.Val118Met | missense_variant | 0.98 |
clpC1 | 4039113 | p.Ala531Asp | missense_variant | 0.97 |
embC | 4242095 | p.Ala745Pro | missense_variant | 1.0 |
embB | 4247621 | c.1108C>T | synonymous_variant | 1.0 |
aftB | 4269585 | c.-749G>A | upstream_gene_variant | 0.98 |
ubiA | 4269776 | p.Ala20Pro | missense_variant | 1.0 |
ethA | 4328211 | c.-739delG | upstream_gene_variant | 1.0 |