Run ID: ERR4818526
Sample name:
Date: 01-04-2023 15:36:27
Number of reads: 284410
Percentage reads mapped: 98.21
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6077 | p.Gly280Cys | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9645 | p.Gly782Ser | missense_variant | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761465 | c.1659G>A | synonymous_variant | 1.0 |
rpoB | 761665 | c.1862delG | frameshift_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764293 | c.924G>C | synonymous_variant | 1.0 |
rpoC | 764553 | p.Gly395Ala | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776499 | p.Gly661Glu | missense_variant | 0.22 |
mmpL5 | 777327 | p.Ala385Gly | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302970 | p.Ser14Gly | missense_variant | 0.25 |
embR | 1417065 | p.Ala95Thr | missense_variant | 1.0 |
atpE | 1461111 | p.Gly23Cys | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.4 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.29 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.25 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156106 | c.6C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168529 | p.Gly695Val | missense_variant | 0.4 |
PPE35 | 2170064 | c.549G>C | synonymous_variant | 0.22 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859752 | p.Gly223Cys | missense_variant | 0.22 |
thyX | 3067199 | c.747A>G | synonymous_variant | 0.17 |
thyA | 3074654 | c.-184delG | upstream_gene_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474094 | p.Glu30Lys | missense_variant | 0.67 |
fprA | 3474726 | c.720G>A | synonymous_variant | 0.5 |
ddn | 3986932 | p.Arg30Leu | missense_variant | 0.25 |
panD | 4044107 | p.Ala59Thr | missense_variant | 0.25 |
embC | 4240081 | c.219G>A | synonymous_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242610 | c.-623A>G | upstream_gene_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243440 | c.208C>T | synonymous_variant | 1.0 |
embB | 4248549 | p.Ala679Val | missense_variant | 0.17 |
embB | 4249242 | p.Leu910Pro | missense_variant | 0.17 |
embB | 4249381 | c.2868A>T | synonymous_variant | 0.18 |
aftB | 4268781 | p.Trp19Leu | missense_variant | 0.33 |
ethA | 4326753 | p.Lys241Glu | missense_variant | 0.17 |
ethR | 4327335 | c.-214A>G | upstream_gene_variant | 0.33 |
ethA | 4328379 | c.-906C>T | upstream_gene_variant | 1.0 |
ethA | 4328412 | c.-939G>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |