Run ID: ERR025832
Sample name:
Date: 31-03-2023 08:17:46
Number of reads: 382338
Percentage reads mapped: 99.01
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.37 |
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 | 0.75 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.62 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.3 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.45 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.83 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.83 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.43 |
mmpS5 | 779565 | c.-660G>A | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471840 | n.-6T>G | upstream_gene_variant | 0.25 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.82 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.88 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.5 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.33 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.22 |
folC | 2747263 | c.336C>A | synonymous_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.86 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.7 |
whiB7 | 3568515 | c.165G>C | synonymous_variant | 0.43 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.29 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.33 |
alr | 3840765 | p.Leu219Pro | missense_variant | 0.29 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.5 |
embC | 4241562 | p.Arg567His | missense_variant | 0.83 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.55 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.43 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.5 |
embB | 4246754 | c.243delC | frameshift_variant | 0.15 |
embB | 4247975 | p.Val488Ile | missense_variant | 0.4 |
embB | 4249531 | p.Ile1006Met | missense_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.33 |
ethA | 4327546 | c.-73T>C | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.44 |
gid | 4407620 | p.Tyr195His | missense_variant | 0.38 |