Run ID: ERR245747
Sample name:
Date: 31-03-2023 18:18:36
Number of reads: 5653710
Percentage reads mapped: 98.93
Strain: lineage3
Drug-resistance: MDR-TB
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 |
---|---|---|---|---|---|
rpoB | 761095 | p.Leu430Pro | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.3 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 762249 | p.Leu815Val | missense_variant | 0.22 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.26 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
rpoC | 765734 | p.Leu789Ala | missense_variant | 1.0 |
rpoC | 767305 | p.Tyr1312* | stop_gained | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800997 | p.Asn63Lys | missense_variant | 0.19 |
embR | 1417501 | c.-154A>C | upstream_gene_variant | 0.27 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.24 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.26 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167871 | c.2742G>C | synonymous_variant | 0.24 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.32 |
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 | 2518144 | c.29dupG | frameshift_variant | 0.11 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.26 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.45 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.17 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641271 | p.Tyr243* | stop_gained | 0.29 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.22 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.26 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.19 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.28 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.43 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.21 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.27 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.3 |
embA | 4243190 | c.-43G>C | upstream_gene_variant | 1.0 |
embA | 4244375 | c.1143C>G | synonymous_variant | 0.35 |
embB | 4247041 | c.528C>T | synonymous_variant | 0.23 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.19 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |