Run ID: SRR6207283
Sample name:
Date: 02-08-2023 15:09:45
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.3.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5863 | c.624G>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491532 | c.750G>C | synonymous_variant | 0.29 |
mshA | 575397 | p.Arg17His | missense_variant | 0.18 |
mshA | 575751 | p.Gly135Glu | missense_variant | 0.11 |
rpoB | 759780 | c.-27T>C | upstream_gene_variant | 0.17 |
rpoB | 761165 | c.1359G>T | synonymous_variant | 0.13 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.1 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.12 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.13 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.12 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.12 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776020 | p.Leu821Val | missense_variant | 0.11 |
mmpL5 | 777621 | p.Glu287Gly | missense_variant | 0.18 |
mmpL5 | 777678 | p.Val268Gly | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1460855 | c.-190_-189insC | upstream_gene_variant | 0.33 |
atpE | 1461040 | c.-4delG | upstream_gene_variant | 0.13 |
atpE | 1461063 | p.Ala7Thr | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472446 | n.601T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472466 | n.621C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472971 | n.1126G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.14 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.2 |
rpsA | 1833706 | c.165C>T | synonymous_variant | 0.12 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155160 | p.Glu318Lys | missense_variant | 0.17 |
katG | 2155477 | p.Gly212Asp | missense_variant | 0.13 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223284 | c.-120C>A | upstream_gene_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290094 | c.-853A>G | upstream_gene_variant | 0.22 |
kasA | 2517947 | c.-168C>A | upstream_gene_variant | 0.11 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.27 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475358 | p.Leu451Ser | missense_variant | 0.33 |
alr | 3841124 | c.297G>A | synonymous_variant | 0.2 |
rpoA | 3878218 | p.Leu97Pro | missense_variant | 0.18 |
rpoA | 3878430 | c.78G>T | synonymous_variant | 0.22 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040241 | p.Thr155Ile | missense_variant | 0.11 |
clpC1 | 4040249 | p.Glu152Gly | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244729 | c.1497C>T | synonymous_variant | 1.0 |
embA | 4245245 | c.2013C>T | synonymous_variant | 0.2 |
embB | 4246825 | p.Lys104Asn | missense_variant | 0.33 |
aftB | 4267445 | c.1392G>T | synonymous_variant | 0.11 |
aftB | 4267933 | p.Ala302Pro | missense_variant | 0.2 |
aftB | 4269108 | c.-272C>A | upstream_gene_variant | 0.12 |
ethA | 4326142 | c.1332C>T | synonymous_variant | 0.17 |
ethA | 4326504 | p.Gly324Arg | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408408 | c.-206G>T | upstream_gene_variant | 0.17 |