Run ID: ERR2228823
Sample name:
Date: 31-03-2023 16:22:14
Number of reads: 324635
Percentage reads mapped: 98.61
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7562 | c.261C>T | synonymous_variant | 0.5 |
gyrA | 9473 | c.2172G>T | synonymous_variant | 0.15 |
rpoB | 763083 | p.Arg1093Ser | missense_variant | 0.29 |
rpoC | 765674 | p.Glu769Gln | missense_variant | 0.67 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.33 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.33 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304268 | c.1338G>T | synonymous_variant | 0.4 |
embR | 1416506 | p.Thr281Ile | missense_variant | 0.29 |
embR | 1417487 | c.-140T>C | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472043 | n.198T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475719 | n.2062G>A | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.33 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.33 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102422 | c.621C>A | synonymous_variant | 0.5 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.5 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.5 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.5 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.25 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.29 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.33 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.33 |
PPE35 | 2169457 | p.His386Asp | missense_variant | 0.15 |
PPE35 | 2169462 | p.Val384Pro | missense_variant | 0.14 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.18 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.22 |
PPE35 | 2169986 | p.Leu209Phe | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.29 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.14 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289182 | c.60G>T | synonymous_variant | 0.25 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.5 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.5 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.5 |
kasA | 2518896 | c.783_784delGT | frameshift_variant | 0.5 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.4 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.4 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.4 |
kasA | 2519338 | c.1224T>C | synonymous_variant | 1.0 |
ahpC | 2725938 | c.-255_-254insA | upstream_gene_variant | 0.15 |
ribD | 2986803 | c.-36A>T | upstream_gene_variant | 0.33 |
Rv2752c | 3066128 | p.Gly22Cys | missense_variant | 0.5 |
thyA | 3074660 | c.-189C>A | upstream_gene_variant | 0.25 |
alr | 3841539 | c.-119C>T | upstream_gene_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
clpC1 | 4038182 | c.2523C>G | synonymous_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248883 | c.2370C>A | synonymous_variant | 1.0 |
embB | 4249449 | p.Gly979Val | missense_variant | 0.2 |
aftB | 4268228 | c.609C>T | synonymous_variant | 0.5 |
aftB | 4269735 | c.-899G>T | upstream_gene_variant | 0.12 |
ethA | 4327064 | p.Cys137Ser | missense_variant | 0.4 |
whiB6 | 4338205 | p.Val106Ala | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |