Run ID: ERR3077959
Sample name:
Date: 01-04-2023 00:12:38
Number of reads: 632460
Percentage reads mapped: 99.46
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575294 | c.-54C>T | upstream_gene_variant | 0.29 |
mshA | 576354 | p.Leu336Pro | missense_variant | 0.11 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.62 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761043 | p.Asn413Asp | missense_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.94 |
rpoC | 762824 | c.-546C>T | upstream_gene_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777471 | p.Val337Ala | missense_variant | 0.13 |
mmpL5 | 778804 | c.-324C>T | upstream_gene_variant | 0.12 |
mmpS5 | 779675 | c.-770G>A | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406671 | p.Val224Ile | missense_variant | 0.15 |
Rv1258c | 1407387 | c.-47T>A | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103199 | c.-157G>A | upstream_gene_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168105 | c.2508C>G | synonymous_variant | 0.11 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 0.9 |
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 |
eis | 2715327 | c.6T>C | synonymous_variant | 0.11 |
eis | 2715505 | c.-173A>G | upstream_gene_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860050 | c.369G>A | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087012 | c.196delG | frameshift_variant | 0.12 |
Rv3083 | 3448596 | c.93A>G | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568737 | c.-58C>T | upstream_gene_variant | 1.0 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.24 |
alr | 3840247 | p.Thr392Ala | missense_variant | 0.14 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243201 | c.-32G>A | upstream_gene_variant | 0.11 |
embB | 4248271 | c.1760delT | frameshift_variant | 0.12 |
ethA | 4328387 | c.-914A>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |