Run ID: SRR6650192
Sample name:
Date: 04-04-2023 15:18:37
Number of reads: 473666
Percentage reads mapped: 99.62
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5332 | c.93C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8168 | p.Glu289Asp | missense_variant | 1.0 |
rpoC | 764431 | c.1066delA | frameshift_variant | 0.17 |
rpoC | 767033 | p.Ser1222Ala | missense_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775734 | p.Phe916Cys | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305303 | c.2373T>G | synonymous_variant | 0.25 |
Rv1258c | 1406462 | c.879C>T | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475567 | n.1910C>A | non_coding_transcript_exon_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101721 | p.Arg441Leu | missense_variant | 0.17 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714887 | p.Phe149Cys | missense_variant | 0.18 |
pepQ | 2860072 | p.Gly116Asp | missense_variant | 0.25 |
Rv2752c | 3065126 | p.Ser356Pro | missense_variant | 0.12 |
ald | 3087714 | p.Ala299Ser | missense_variant | 0.13 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
panD | 4044356 | c.-75T>C | upstream_gene_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245010 | p.Ala593Val | missense_variant | 0.4 |
embA | 4245417 | p.Gly729Arg | missense_variant | 1.0 |
embA | 4246368 | p.Leu1046Met | missense_variant | 0.25 |
embB | 4246596 | p.Trp28Leu | missense_variant | 0.17 |
embB | 4248542 | p.Ala677Ser | missense_variant | 0.22 |
embB | 4249010 | c.2497C>T | synonymous_variant | 0.15 |
aftB | 4268568 | p.Leu90Arg | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407712 | p.Gly164Asp | missense_variant | 1.0 |