Run ID: ERR4815772
Sample name:
Date: 01-04-2023 14:03:13
Number of reads: 516786
Percentage reads mapped: 94.63
Strain: lineage4.4.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
thyA | 3074095 | p.Arg126Gln | missense_variant | 0.12 | para-aminosalicylic_acid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5107 | c.-133C>A | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9026 | c.1725G>A | synonymous_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9635 | c.2334T>C | synonymous_variant | 0.1 |
mshA | 576142 | c.795G>A | synonymous_variant | 0.12 |
rpoB | 760537 | p.Glu244Val | missense_variant | 0.29 |
rpoC | 763802 | p.His145Tyr | missense_variant | 0.4 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.2 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.2 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.2 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.2 |
rpoC | 764668 | c.1299C>A | synonymous_variant | 0.18 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.18 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.15 |
rpoC | 766524 | p.Arg1052Gln | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777258 | c.1222delC | frameshift_variant | 0.14 |
mmpR5 | 778025 | c.-965T>C | upstream_gene_variant | 0.13 |
mmpL5 | 778357 | p.Thr42Ser | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303065 | c.135C>T | synonymous_variant | 0.17 |
fbiC | 1304350 | p.Glu474Gln | missense_variant | 0.2 |
fbiC | 1305313 | p.Arg795Gly | missense_variant | 0.14 |
embR | 1416637 | p.Asp237Glu | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472841 | n.996G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.67 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673947 | p.Glu170Lys | missense_variant | 0.17 |
inhA | 1674493 | p.Met98Leu | missense_variant | 0.25 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.25 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.29 |
rpsA | 1834057 | c.516G>A | synonymous_variant | 0.29 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.4 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.17 |
rpsA | 1834213 | c.672G>A | synonymous_variant | 0.15 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.14 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.16 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.16 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.15 |
rpsA | 1834788 | p.Ala416Asp | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102389 | c.653delC | frameshift_variant | 0.14 |
ndh | 2102550 | p.Glu165Gln | missense_variant | 0.18 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2155455 | c.657G>T | synonymous_variant | 0.22 |
katG | 2156569 | c.-458C>T | upstream_gene_variant | 0.4 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170413 | p.Ala67Val | missense_variant | 0.2 |
Rv1979c | 2222532 | c.633C>A | synonymous_variant | 0.22 |
Rv1979c | 2222729 | p.Gly146Ser | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289723 | c.-482C>A | upstream_gene_variant | 0.2 |
eis | 2714136 | c.1197G>C | synonymous_variant | 0.12 |
ahpC | 2726046 | c.-147G>T | upstream_gene_variant | 0.18 |
folC | 2746229 | p.Ala457Val | missense_variant | 0.12 |
folC | 2747228 | c.370delT | frameshift_variant | 0.17 |
folC | 2747625 | c.-27C>T | upstream_gene_variant | 0.2 |
thyA | 3074440 | p.Val11Ala | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087491 | c.672G>A | synonymous_variant | 0.15 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474417 | p.His137Gln | missense_variant | 0.18 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
fbiB | 3641037 | c.-498G>A | upstream_gene_variant | 0.11 |
fbiB | 3642006 | p.Asn158Asp | missense_variant | 0.17 |
alr | 3841459 | c.-39C>T | upstream_gene_variant | 0.17 |
panD | 4044443 | c.-162G>A | upstream_gene_variant | 0.12 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.11 |
embC | 4242607 | p.Met915Ile | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244681 | c.1449A>G | synonymous_variant | 0.11 |
embA | 4245389 | c.2157C>A | synonymous_variant | 0.11 |
embB | 4247584 | c.1074delG | frameshift_variant | 0.17 |
embB | 4248285 | p.Lys591Met | missense_variant | 0.29 |
ubiA | 4268963 | p.Trp291Arg | missense_variant | 0.12 |
ubiA | 4269429 | p.Gln135His | missense_variant | 0.22 |
ethA | 4326692 | p.Arg261Gln | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408219 | c.-17A>G | upstream_gene_variant | 0.12 |