Run ID: ERR2229813
Sample name:
Date: 31-03-2023 17:36:33
Number of reads: 617907
Percentage reads mapped: 99.66
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491475 | c.693C>A | synonymous_variant | 0.22 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
rpoC | 766025 | p.Val886Met | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406234 | c.1107A>G | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471856 | n.11A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473423 | n.-235C>A | upstream_gene_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476012 | n.2355T>C | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.15 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.17 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.13 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519346 | p.Leu411Pro | missense_variant | 0.12 |
thyX | 3067795 | p.Asn51Asp | missense_variant | 0.17 |
ald | 3086622 | c.-198C>T | upstream_gene_variant | 0.15 |
ald | 3086624 | c.-196T>C | upstream_gene_variant | 0.15 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.17 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.18 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.15 |
clpC1 | 4039530 | p.Asp392Ala | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249392 | p.Trp960Leu | missense_variant | 0.13 |
aftB | 4267190 | c.1647T>A | synonymous_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |