Run ID: SRR18912067
Sample name:
Date: 03-04-2023 20:48:16
Number of reads: 106908
Percentage reads mapped: 99.66
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6127 | c.888G>T | synonymous_variant | 0.25 |
gyrA | 6328 | c.-974C>T | upstream_gene_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7555 | p.His85Arg | missense_variant | 0.67 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8983 | p.Cys561Phe | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9687 | p.Arg796Trp | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619950 | c.60G>A | synonymous_variant | 0.4 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 0.25 |
rpoB | 762405 | p.Val867Leu | missense_variant | 0.33 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 764718 | p.Glu450Gly | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781629 | p.Leu24Val | missense_variant | 0.67 |
rplC | 800635 | c.-174G>A | upstream_gene_variant | 0.67 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.36 |
fbiC | 1305075 | p.Ser715Arg | missense_variant | 0.29 |
fbiC | 1305443 | p.Glu838Val | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472002 | n.157A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473260 | n.1415G>A | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102734 | c.309G>A | synonymous_variant | 0.25 |
katG | 2154155 | p.Leu653Met | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156429 | c.-318C>T | upstream_gene_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289878 | c.-637C>T | upstream_gene_variant | 0.4 |
kasA | 2518917 | p.Ala268Val | missense_variant | 0.4 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2987187 | c.349C>T | synonymous_variant | 1.0 |
Rv2752c | 3065159 | p.Glu345* | stop_gained | 0.67 |
Rv2752c | 3065694 | c.498G>A | synonymous_variant | 0.33 |
thyX | 3067592 | c.354G>T | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641755 | p.Arg74His | missense_variant | 0.33 |
alr | 3841204 | p.Gly73Ser | missense_variant | 0.29 |
alr | 3841299 | p.Asp41Gly | missense_variant | 0.2 |
clpC1 | 4038660 | c.2044delT | frameshift_variant | 0.14 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.4 |
panD | 4043995 | p.Ala96Asp | missense_variant | 0.4 |
embC | 4239788 | c.-75C>T | upstream_gene_variant | 0.33 |
embC | 4239883 | c.25delC | frameshift_variant | 0.18 |
embC | 4239907 | c.45A>C | synonymous_variant | 0.15 |
embC | 4240862 | p.Trp334Arg | missense_variant | 0.4 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246921 | c.408G>C | synonymous_variant | 1.0 |
embB | 4249399 | c.2886G>T | synonymous_variant | 1.0 |
ethA | 4326152 | p.Arg441His | missense_variant | 0.29 |
ethA | 4326291 | p.Ala395Thr | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407880 | p.Leu108Gln | missense_variant | 0.25 |
gid | 4407980 | p.Pro75Ser | missense_variant | 1.0 |