Run ID: ERR10796548
Sample name:
Date: 31-03-2023 11:11:08
Number of reads: 794473
Percentage reads mapped: 100.0
Strain: lineage4.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5082 | c.-157delC | upstream_gene_variant | 1.0 |
gyrB | 6507 | p.Ala423Val | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.11 |
gyrA | 9165 | p.Tyr622His | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9656 | c.2355C>G | synonymous_variant | 1.0 |
ccsA | 619792 | c.-99C>T | upstream_gene_variant | 0.4 |
rpoB | 762958 | p.Leu1051Pro | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765187 | c.1818C>T | synonymous_variant | 1.0 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
rplC | 801275 | p.Thr156Met | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474198 | n.541G>T | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1833711 | c.171delC | frameshift_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156007 | c.105C>T | synonymous_variant | 1.0 |
Rv1979c | 2222451 | c.714C>T | synonymous_variant | 0.11 |
Rv1979c | 2222759 | p.Val136Met | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288993 | c.249C>T | synonymous_variant | 1.0 |
pepQ | 2859857 | p.Val188Met | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474235 | c.230delG | frameshift_variant | 0.14 |
alr | 3840605 | c.816G>T | synonymous_variant | 0.13 |
ddn | 3986691 | c.-153G>C | upstream_gene_variant | 0.15 |
clpC1 | 4039028 | c.1676delA | frameshift_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243884 | p.Met218Leu | missense_variant | 0.2 |
embB | 4246817 | p.Ala102Thr | missense_variant | 0.13 |
aftB | 4268391 | p.Gly149Val | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408237 | c.-35C>T | upstream_gene_variant | 0.18 |