Run ID: SRR9588015
Sample name:
Date: 02-08-2023 15:29:13
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.4.1.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761277 | p.Ile491Phe | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289091 | p.His51Asp | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491316 | c.534C>G | synonymous_variant | 0.12 |
mshA | 576734 | c.1387C>T | synonymous_variant | 0.13 |
ccsA | 620619 | c.729G>A | synonymous_variant | 0.11 |
rpoC | 766467 | p.Glu1033Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777042 | c.1438delC | frameshift_variant | 0.1 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801143 | p.Val112Ala | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.17 |
rpsA | 1833726 | p.Val62Ala | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518496 | c.382C>T | synonymous_variant | 1.0 |
eis | 2715354 | c.-22G>A | upstream_gene_variant | 0.11 |
folC | 2747608 | c.-10C>A | upstream_gene_variant | 0.1 |
pepQ | 2859944 | p.Ala159Ser | missense_variant | 0.14 |
ribD | 2986911 | p.Asp25Asn | missense_variant | 0.12 |
ribD | 2987404 | p.Arg189Leu | missense_variant | 0.11 |
Rv2752c | 3065023 | p.Pro390Leu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448522 | p.Val7Phe | missense_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3448748 | p.Arg82Gln | missense_variant | 0.12 |
Rv3083 | 3449105 | p.Pro201His | missense_variant | 0.22 |
Rv3083 | 3449552 | p.Ile350Thr | missense_variant | 0.1 |
Rv3083 | 3449606 | p.Pro368Leu | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474802 | p.Arg266Gly | missense_variant | 0.12 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244847 | p.Gly539Cys | missense_variant | 0.2 |
embA | 4244984 | p.Leu584Phe | missense_variant | 0.12 |
embB | 4249425 | p.Leu971Pro | missense_variant | 0.11 |
aftB | 4268888 | c.-52C>A | upstream_gene_variant | 0.14 |
ubiA | 4269299 | p.Ile179Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408034 | c.168_169insCG | frameshift_variant | 0.13 |