Run ID: SRR6785216
Sample name:
Date: 04-04-2023 15:37:11
Number of reads: 1945662
Percentage reads mapped: 99.75
Strain: lineage4.8
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6076 | c.837C>T | synonymous_variant | 0.15 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.26 |
rpoB | 759640 | c.-167G>T | upstream_gene_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474880 | n.1223T>C | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168076 | p.Thr846Met | missense_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169125 | c.1488T>C | synonymous_variant | 0.15 |
PPE35 | 2169198 | p.Val472Ala | missense_variant | 0.12 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.11 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.14 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.18 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.2 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.15 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.19 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.14 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.13 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245751 | c.2522delG | frameshift_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.21 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.21 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.2 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.2 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.3 |
embB | 4246669 | c.156C>A | synonymous_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv1979c | 2222416 | c.-597_748del | frameshift_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |