Run ID: ERR4814437
Sample name:
Date: 01-04-2023 13:17:41
Number of reads: 906354
Percentage reads mapped: 99.34
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1917940 | c.2delT | frameshift_variant | 0.12 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8906 | c.1605C>A | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491316 | c.534C>G | synonymous_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619864 | c.-27G>A | upstream_gene_variant | 0.2 |
ccsA | 620855 | p.Gly322Val | missense_variant | 1.0 |
rpoB | 759852 | p.Ser16Cys | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.19 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776092 | p.Ser797Arg | missense_variant | 0.1 |
mmpL5 | 777824 | p.Leu219Phe | missense_variant | 1.0 |
mmpL5 | 778242 | p.Lys80Met | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.35 |
embR | 1416786 | p.Ser188Gly | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102389 | c.654G>C | synonymous_variant | 0.25 |
ndh | 2102392 | c.651C>A | synonymous_variant | 0.24 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.38 |
ndh | 2102407 | c.636T>C | synonymous_variant | 0.13 |
ndh | 2102739 | p.Glu102* | stop_gained | 0.14 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.12 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.11 |
PPE35 | 2169272 | c.1341C>A | synonymous_variant | 0.11 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
PPE35 | 2169789 | p.Leu275* | stop_gained | 0.12 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.16 |
PPE35 | 2169974 | c.639T>C | synonymous_variant | 0.11 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.97 |
folC | 2746999 | p.Asp200Glu | missense_variant | 0.11 |
thyA | 3074346 | c.126C>T | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.1 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.11 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.11 |
clpC1 | 4040027 | c.678C>G | synonymous_variant | 0.11 |
clpC1 | 4040032 | p.Val225Ile | missense_variant | 0.11 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.12 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242660 | p.Leu933Gln | missense_variant | 0.15 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4246285 | p.Ser1018Leu | missense_variant | 0.11 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |