Run ID: ERR3077960
Sample name:
Date: 01-04-2023 00:12:44
Number of reads: 423686
Percentage reads mapped: 99.28
Strain: lineage4.2.2
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 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761100 | p.Gln432Glu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Met | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6375 | p.Glu379Gly | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9155 | c.1854C>A | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9720 | p.Gly807Cys | missense_variant | 0.12 |
fgd1 | 490936 | p.Pro52Thr | missense_variant | 0.13 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.6 |
rpoB | 759981 | p.Ile59Phe | missense_variant | 0.15 |
rpoB | 761248 | p.Glu481Ala | missense_variant | 1.0 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 1.0 |
rpoB | 762112 | p.Asn769Thr | missense_variant | 1.0 |
rpoB | 762977 | p.Phe1057Leu | missense_variant | 0.2 |
rpoC | 765358 | p.Met663Ile | missense_variant | 0.17 |
rpoC | 766966 | p.Glu1199Asp | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775736 | c.2745C>A | synonymous_variant | 0.2 |
mmpL5 | 775853 | c.2628C>T | synonymous_variant | 0.15 |
mmpR5 | 779370 | p.Asp127Glu | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781653 | p.Gly32Ser | missense_variant | 0.2 |
rplC | 801229 | c.424dupC | frameshift_variant | 0.14 |
fbiC | 1303041 | c.112delA | frameshift_variant | 0.4 |
fbiC | 1303517 | p.Met196Lys | missense_variant | 0.2 |
fbiC | 1304929 | p.Thr667Ala | missense_variant | 0.17 |
Rv1258c | 1406405 | c.936G>A | synonymous_variant | 0.18 |
Rv1258c | 1406432 | p.Met303Ile | missense_variant | 0.13 |
embR | 1416787 | c.561C>A | synonymous_variant | 0.14 |
embR | 1416971 | p.Ala126Asp | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475259 | n.1602T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475337 | n.1680C>T | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101981 | c.1062C>A | synonymous_variant | 0.12 |
ndh | 2102196 | p.Ser283Gly | missense_variant | 0.12 |
katG | 2155478 | p.Gly212Ser | missense_variant | 0.17 |
PPE35 | 2169895 | p.Gly240Cys | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288911 | p.Glu111* | stop_gained | 1.0 |
pncA | 2288972 | c.270C>A | synonymous_variant | 0.15 |
eis | 2715470 | c.-138G>T | upstream_gene_variant | 0.22 |
folC | 2746270 | c.1329C>A | synonymous_variant | 0.25 |
folC | 2746388 | p.Thr404Ile | missense_variant | 0.22 |
folC | 2746684 | c.915C>G | synonymous_variant | 0.14 |
folC | 2746909 | c.690C>A | synonymous_variant | 0.2 |
folC | 2747485 | p.Trp38* | stop_gained | 0.17 |
ribD | 2986985 | c.147G>A | synonymous_variant | 0.17 |
ribD | 2987209 | p.Gly124Ala | missense_variant | 0.15 |
Rv2752c | 3065319 | c.873C>T | synonymous_variant | 0.29 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
thyX | 3067479 | p.Asp156Val | missense_variant | 0.33 |
thyA | 3074641 | c.-170C>T | upstream_gene_variant | 0.4 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475325 | p.Pro440Arg | missense_variant | 0.18 |
Rv3236c | 3612746 | c.370dupG | frameshift_variant | 0.29 |
fbiB | 3642801 | p.Ala423Pro | missense_variant | 0.22 |
fbiB | 3642805 | p.Ile424Thr | missense_variant | 0.25 |
alr | 3841348 | p.Met25Leu | missense_variant | 0.18 |
rpoA | 3877506 | c.1001delG | frameshift_variant | 0.15 |
panD | 4044374 | c.-93G>A | upstream_gene_variant | 0.22 |
embC | 4241983 | c.2121G>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244830 | p.Phe533Tyr | missense_variant | 0.12 |
embA | 4244848 | p.Gly539Val | missense_variant | 0.14 |
embB | 4246022 | c.-492C>A | upstream_gene_variant | 0.22 |
embA | 4246314 | p.Gly1028Cys | missense_variant | 0.22 |
embA | 4246434 | p.Gln1068Lys | missense_variant | 0.15 |
embB | 4248028 | c.1515C>T | synonymous_variant | 0.18 |
aftB | 4267531 | p.Ala436Ser | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |