Run ID: ERR11044895
Sample name:
Date: 31-03-2023 12:02:21
Number of reads: 375680
Percentage reads mapped: 99.4
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 |
---|---|---|---|---|
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 | 9596 | c.2295G>T | synonymous_variant | 1.0 |
gyrA | 9777 | p.Asn826Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575991 | p.Val215Asp | missense_variant | 0.18 |
mshA | 576100 | p.Asp251Glu | missense_variant | 0.22 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.33 |
ccsA | 620865 | c.975A>T | stop_lost&splice_region_variant | 0.22 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761401 | p.Arg532Leu | missense_variant | 0.18 |
rpoB | 761482 | p.Ala559Gly | missense_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762636 | p.Lys944Glu | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
rpoC | 764365 | c.996C>G | synonymous_variant | 0.22 |
rpoC | 764953 | c.1584G>A | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778154 | c.-836G>A | upstream_gene_variant | 0.18 |
mmpL5 | 778668 | c.-188C>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472194 | n.349G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474008 | n.351G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474978 | n.1321A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475367 | n.1710C>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834853 | p.Ala438Thr | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918535 | p.His199Leu | missense_variant | 0.22 |
ndh | 2101759 | c.1284G>A | synonymous_variant | 0.12 |
ndh | 2101891 | c.1152C>A | synonymous_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168085 | p.Glu843Gly | missense_variant | 0.29 |
PPE35 | 2169216 | p.Glu466Val | missense_variant | 0.13 |
PPE35 | 2170517 | c.96C>T | synonymous_variant | 0.11 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_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 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.67 |
eis | 2715427 | c.-95T>G | upstream_gene_variant | 0.29 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859359 | p.Thr354Ala | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.33 |
Rv2752c | 3065499 | c.693A>G | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474087 | c.81C>T | synonymous_variant | 0.2 |
fprA | 3474525 | p.Leu173Phe | missense_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245825 | p.Asp865Asn | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407560 | p.Ser215Pro | missense_variant | 0.13 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |