Run ID: ERR4818944
Sample name:
Date: 01-04-2023 15:50:21
Number of reads: 494533
Percentage reads mapped: 99.39
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 | 6689 | p.Lys484Glu | missense_variant | 0.4 |
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 | 490745 | c.-38G>A | upstream_gene_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760082 | c.276C>T | synonymous_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764058 | p.Ala230Val | missense_variant | 1.0 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776673 | p.Val603Gly | missense_variant | 0.18 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.18 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.24 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302959 | p.Thr10Ile | missense_variant | 0.12 |
fbiC | 1305188 | p.Leu753Pro | missense_variant | 0.13 |
Rv1258c | 1407098 | c.243G>A | synonymous_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.12 |
rpsA | 1833491 | c.-51A>T | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103097 | c.-55C>A | upstream_gene_variant | 0.2 |
ndh | 2103113 | c.-71C>T | upstream_gene_variant | 0.29 |
katG | 2154667 | p.Ser482Leu | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155624 | p.Asp163Gly | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.11 |
PPE35 | 2168059 | p.Gln852Glu | missense_variant | 0.15 |
PPE35 | 2168068 | p.Phe849Leu | missense_variant | 0.12 |
PPE35 | 2168070 | p.Glu848Pro | missense_variant | 0.12 |
PPE35 | 2168860 | p.Ser585Gly | missense_variant | 0.2 |
PPE35 | 2169125 | p.Val496Ile | missense_variant | 0.22 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.4 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.29 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.19 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.21 |
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 |
pncA | 2289510 | c.-269G>C | upstream_gene_variant | 0.33 |
kasA | 2519321 | p.Gly403Arg | missense_variant | 0.4 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860294 | p.Ala42Glu | missense_variant | 0.2 |
Rv2752c | 3065078 | p.Val372Ile | missense_variant | 0.14 |
thyX | 3067964 | c.-19C>T | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449492 | p.Leu330Pro | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840576 | p.Ala282Glu | missense_variant | 0.15 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.2 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.2 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.12 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.13 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.17 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.15 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.15 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
clpC1 | 4040494 | p.Gln71Lys | missense_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.91 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244659 | p.Leu476Pro | missense_variant | 0.17 |
embA | 4244666 | c.1434G>C | synonymous_variant | 0.13 |
ethR | 4327324 | c.-225A>G | upstream_gene_variant | 0.2 |
ethR | 4327327 | c.-222A>G | upstream_gene_variant | 0.2 |
ethR | 4327336 | c.-213A>G | upstream_gene_variant | 0.18 |
whiB6 | 4338424 | p.Val33Ala | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408059 | c.144T>C | synonymous_variant | 0.13 |