Run ID: ERR2229121
Sample name:
Date: 31-03-2023 16:42:26
Number of reads: 875693
Percentage reads mapped: 99.46
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491502 | p.Glu240Asp | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.42 |
rpoB | 761869 | p.Asp688Val | missense_variant | 0.12 |
rpoC | 764026 | p.Leu219Phe | missense_variant | 0.2 |
rpoC | 764766 | p.Ala466Glu | missense_variant | 0.12 |
rpoC | 765006 | c.1640delT | frameshift_variant | 0.15 |
rpoC | 765459 | p.Ile697Asn | missense_variant | 0.12 |
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 |
atpE | 1460913 | c.-132G>A | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472207 | n.362A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473651 | n.-7G>A | upstream_gene_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.16 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.36 |
fabG1 | 1674009 | p.Met190Ile | missense_variant | 0.12 |
rpsA | 1834892 | p.Ala451Thr | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102450 | p.Lys198Arg | missense_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168812 | p.Thr601Ser | missense_variant | 0.12 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.16 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.11 |
PPE35 | 2169882 | p.Ser244Asn | missense_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.3 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289542 | c.-302delG | upstream_gene_variant | 0.13 |
pncA | 2289550 | c.-310delC | upstream_gene_variant | 0.13 |
kasA | 2518685 | p.Asp191Asn | missense_variant | 0.17 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.12 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.13 |
eis | 2714170 | p.Ala388Glu | missense_variant | 0.15 |
eis | 2715155 | p.Gly60Arg | missense_variant | 0.12 |
ahpC | 2726188 | c.-5G>T | upstream_gene_variant | 0.12 |
ald | 3087316 | p.Val166Ala | missense_variant | 0.18 |
ald | 3087319 | c.500_501insTC | frameshift_variant | 0.18 |
ald | 3087334 | p.Val172Ala | missense_variant | 0.25 |
ald | 3087337 | c.519_520delGA | frameshift_variant | 0.22 |
ald | 3087343 | p.Gly175Asp | missense_variant | 0.22 |
fbiD | 3339711 | c.594A>T | synonymous_variant | 0.12 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.13 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.14 |
rpoA | 3877691 | p.Gly273Ser | missense_variant | 0.12 |
embC | 4240923 | p.Thr354Asn | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244898 | p.Thr556Ser | missense_variant | 0.22 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.36 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
embB | 4247028 | p.Leu172Gln | missense_variant | 0.29 |
embB | 4248617 | p.Leu702Met | missense_variant | 0.13 |
embB | 4249339 | c.2826T>C | synonymous_variant | 0.14 |
ethA | 4328434 | c.-961C>A | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |