Run ID: ERR11050176
Sample name:
Date: 02-04-2023 14:54:14
Number of reads: 318547
Percentage reads mapped: 99.45
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7689 | p.Thr130Ser | missense_variant | 0.5 |
gyrA | 8206 | p.Ile302Thr | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760220 | c.414C>T | synonymous_variant | 0.17 |
rpoB | 761571 | p.Pro589Thr | missense_variant | 0.29 |
rpoB | 762540 | p.Asn912Tyr | missense_variant | 0.33 |
rpoB | 763087 | p.Val1094Gly | missense_variant | 0.25 |
rpoC | 764171 | p.Phe268Ile | missense_variant | 0.33 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766591 | p.Glu1074Asp | missense_variant | 0.33 |
rpoC | 766703 | p.Met1112Val | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303956 | p.Glu342Asp | missense_variant | 0.33 |
fbiC | 1303966 | p.Leu346Val | missense_variant | 0.29 |
fbiC | 1305477 | c.2547C>T | synonymous_variant | 0.22 |
embR | 1416697 | c.651C>T | synonymous_variant | 0.43 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473412 | n.-246T>G | upstream_gene_variant | 0.21 |
rrl | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.56 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.75 |
rpsA | 1833676 | p.Lys45Asn | missense_variant | 0.29 |
rpsA | 1834371 | p.Lys277Thr | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170573 | p.Leu14Val | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.4 |
folC | 2747409 | p.Tyr64Asn | missense_variant | 0.18 |
folC | 2747416 | p.Gln61His | missense_variant | 0.22 |
ribD | 2987386 | p.Ala183Val | missense_variant | 0.29 |
ribD | 2987498 | c.660C>G | synonymous_variant | 0.4 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.33 |
Rv2752c | 3065739 | c.453G>A | synonymous_variant | 0.22 |
Rv2752c | 3067053 | c.-862C>T | upstream_gene_variant | 0.17 |
thyA | 3074671 | c.-200G>A | upstream_gene_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087361 | p.Tyr181Phe | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568759 | c.-80A>T | upstream_gene_variant | 0.33 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
fbiA | 3640414 | c.-129G>C | upstream_gene_variant | 0.13 |
fbiB | 3642149 | c.615C>G | synonymous_variant | 0.29 |
fbiB | 3642233 | c.699G>A | synonymous_variant | 0.5 |
alr | 3840549 | p.Glu291Ala | missense_variant | 0.29 |
rpoA | 3877885 | p.Leu208Gln | missense_variant | 0.29 |
rpoA | 3878306 | p.Gly68Arg | missense_variant | 0.22 |
ddn | 3987097 | p.Asn85Ile | missense_variant | 0.17 |
clpC1 | 4039738 | p.Thr323Pro | missense_variant | 0.4 |
clpC1 | 4039822 | p.Ala295Pro | missense_variant | 0.18 |
panD | 4044268 | p.Met5Arg | missense_variant | 0.33 |
embC | 4241059 | c.1197G>A | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243585 | p.Phe118Ser | missense_variant | 0.33 |
embA | 4246383 | p.Tyr1051Asn | missense_variant | 0.2 |
embB | 4247445 | p.Asp311Ala | missense_variant | 0.3 |
aftB | 4267400 | c.1437G>C | synonymous_variant | 0.31 |
ethA | 4327409 | p.His22Leu | missense_variant | 0.2 |
whiB6 | 4338449 | p.Ala25Thr | missense_variant | 0.22 |
whiB6 | 4338491 | p.Thr11Ser | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407970 | p.Pro78Gln | missense_variant | 0.33 |
gid | 4407995 | p.Ser70Cys | missense_variant | 0.33 |
gid | 4408003 | p.Asp67Gly | missense_variant | 0.29 |