Run ID: ERR4816201
Sample name:
Date: 01-04-2023 14:17:46
Number of reads: 905829
Percentage reads mapped: 99.59
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288775 | p.Leu156Pro | missense_variant | 0.1 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575161 | c.-187T>A | upstream_gene_variant | 0.25 |
mshA | 575175 | c.-173G>A | upstream_gene_variant | 0.18 |
mshA | 576500 | p.Ile385Leu | missense_variant | 0.15 |
ccsA | 619813 | c.-78C>A | upstream_gene_variant | 0.17 |
ccsA | 620461 | p.Val191Phe | missense_variant | 0.1 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.21 |
rpoC | 763355 | c.-15G>A | upstream_gene_variant | 1.0 |
rpoC | 765158 | p.Gly597Ser | missense_variant | 0.11 |
rpoC | 766490 | p.Arg1041Gly | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302983 | p.Pro18Leu | missense_variant | 1.0 |
fbiC | 1304070 | c.1140C>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833423 | c.-119C>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.11 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.24 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726552 | c.360A>G | synonymous_variant | 0.11 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3236c | 3612375 | p.Gly248Ser | missense_variant | 0.11 |
Rv3236c | 3612955 | c.162C>T | synonymous_variant | 0.25 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244902 | p.Ala557Glu | missense_variant | 0.2 |
embA | 4245484 | p.Gln751Pro | missense_variant | 0.12 |
embA | 4245756 | c.2525dupG | frameshift_variant | 0.11 |
embB | 4247749 | c.1236G>T | synonymous_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |