Run ID: ERR11043873
Sample name:
Date: 31-03-2023 11:42:44
Number of reads: 432237
Percentage reads mapped: 99.57
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 |
---|---|---|---|---|
gyrB | 6173 | p.Glu312Gln | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575839 | c.492G>A | synonymous_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761398 | p.Asp531Gly | missense_variant | 0.18 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766364 | p.Ala999Thr | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776031 | p.Gly817Glu | missense_variant | 0.25 |
mmpL5 | 776083 | p.Ala800Thr | missense_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776908 | p.Gln525* | stop_gained | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.14 |
embR | 1416216 | p.Phe378Leu | missense_variant | 0.11 |
embR | 1416580 | c.768T>C | synonymous_variant | 0.13 |
atpE | 1460878 | c.-167C>T | upstream_gene_variant | 0.17 |
atpE | 1461160 | p.Val39Gly | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473962 | n.305T>A | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674670 | p.Ala157Thr | missense_variant | 0.12 |
rpsA | 1833551 | p.Pro4Thr | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168896 | p.Gly573Cys | missense_variant | 0.23 |
PPE35 | 2168926 | p.Val563Leu | missense_variant | 0.18 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
PPE35 | 2170545 | p.Pro23Leu | missense_variant | 0.12 |
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 | 2714896 | p.Phe146Ser | missense_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064844 | p.Asp450Asn | missense_variant | 0.22 |
Rv2752c | 3067039 | c.-848T>A | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841394 | c.26delG | frameshift_variant | 0.14 |
clpC1 | 4039830 | p.Leu292Ser | missense_variant | 0.13 |
panD | 4044079 | p.Val68Gly | missense_variant | 0.12 |
embC | 4239705 | c.-158T>A | upstream_gene_variant | 0.17 |
embC | 4240133 | p.Ala91Thr | missense_variant | 0.15 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
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 |
embC | 4242834 | p.Phe991Ser | missense_variant | 0.11 |
embC | 4242963 | p.Gly1034Asp | missense_variant | 0.14 |
whiB6 | 4338470 | p.Asn18Asp | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408345 | c.-143C>T | upstream_gene_variant | 1.0 |