Run ID: SRR18911131
Sample name:
Date: 03-04-2023 20:41:01
Number of reads: 596228
Percentage reads mapped: 99.54
Strain: lineage4.4.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.2 | Euro-American | T1;T2 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490824 | c.42A>G | synonymous_variant | 0.95 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.36 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.25 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778895 | p.Thr4Asn | missense_variant | 0.11 |
mmpR5 | 779228 | p.Ile80Thr | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475187 | n.1530C>G | non_coding_transcript_exon_variant | 0.2 |
inhA | 1673952 | c.-250G>A | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2222778 | p.Asp129Glu | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518492 | p.Tyr126* | stop_gained | 0.12 |
eis | 2714570 | p.Ala255Ser | missense_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.23 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
ald | 3086712 | c.-108C>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568628 | c.52T>C | synonymous_variant | 0.11 |
clpC1 | 4038565 | p.Asp714Asn | missense_variant | 1.0 |
embC | 4241527 | c.1665C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244967 | p.Gly579Trp | missense_variant | 0.2 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407535 | p.Thr223Met | missense_variant | 1.0 |