Run ID: SRR4035549
Sample name:
Date: 04-04-2023 07:10:14
Number of reads: 940126
Percentage reads mapped: 99.39
Strain: lineage3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
katG | 2155149 | p.Trp321Cys | missense_variant | 0.12 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5656 | c.417C>A | synonymous_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7899 | p.Ala200Thr | missense_variant | 0.14 |
gyrA | 8056 | p.Arg252Leu | missense_variant | 1.0 |
gyrA | 8870 | c.1569G>T | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760545 | p.Gly247Trp | missense_variant | 0.17 |
rpoB | 761055 | p.Val417Phe | missense_variant | 0.22 |
rpoB | 761970 | p.Gly722Cys | missense_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762623 | p.Lys939Asn | missense_variant | 0.14 |
rpoB | 762926 | c.3123delG | frameshift_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775609 | c.2868_2871delATCG | frameshift_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777041 | c.1440G>T | synonymous_variant | 0.17 |
mmpL5 | 777780 | p.Thr234Arg | missense_variant | 0.25 |
mmpR5 | 777992 | c.-998G>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781718 | c.159C>A | synonymous_variant | 0.12 |
rplC | 800991 | p.Lys61Asn | missense_variant | 0.14 |
fbiC | 1304807 | p.Pro626His | missense_variant | 0.12 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.12 |
fbiC | 1305372 | p.Glu814Asp | missense_variant | 0.18 |
embR | 1416659 | c.688delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473580 | n.-78G>T | upstream_gene_variant | 0.12 |
rrl | 1475793 | n.2139delA | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674304 | p.Gln35Lys | missense_variant | 0.12 |
rpsA | 1833507 | c.-35C>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918201 | p.Asp88Tyr | missense_variant | 0.18 |
ndh | 2101913 | c.1129delT | frameshift_variant | 0.2 |
ndh | 2103114 | c.-72G>T | upstream_gene_variant | 0.13 |
ndh | 2103214 | c.-172T>G | upstream_gene_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156487 | c.-377delC | upstream_gene_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | 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 | 2290189 | c.-948G>A | upstream_gene_variant | 0.12 |
kasA | 2518110 | c.-5T>G | upstream_gene_variant | 0.15 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.16 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.32 |
pepQ | 2859720 | p.Met233Ile | missense_variant | 0.14 |
pepQ | 2859816 | c.603G>A | synonymous_variant | 0.14 |
pepQ | 2860245 | c.174C>A | synonymous_variant | 0.25 |
ribD | 2986800 | c.-39T>C | upstream_gene_variant | 0.1 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.18 |
Rv2752c | 3064663 | p.Lys510Arg | missense_variant | 0.14 |
Rv2752c | 3064985 | c.1207C>T | synonymous_variant | 0.12 |
Rv2752c | 3065673 | p.Phe173Leu | missense_variant | 0.15 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.29 |
thyA | 3074424 | c.48G>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449054 | p.Gly184Asp | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474179 | p.Pro58His | missense_variant | 0.13 |
fprA | 3474658 | p.Leu218Ile | missense_variant | 0.18 |
fbiB | 3642622 | p.Ala363Val | missense_variant | 0.12 |
clpC1 | 4038292 | p.Asp805Tyr | missense_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243745 | c.513C>A | synonymous_variant | 0.14 |
aftB | 4268770 | p.Gln23* | stop_gained | 0.29 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 1.0 |
whiB6 | 4338312 | c.210G>T | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |