Run ID: SRR18391698
Sample name:
Date: 03-04-2023 19:40:19
Number of reads: 534522
Percentage reads mapped: 97.68
Strain: La1.7.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.7 | M.bovis | None | None | 1.0 |
La1.7.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrB | 6883 | p.Leu548Phe | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490749 | c.-34G>T | upstream_gene_variant | 0.12 |
fgd1 | 491379 | c.597C>T | synonymous_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576549 | p.Ala401Gly | missense_variant | 0.11 |
rpoB | 759793 | c.-14T>C | upstream_gene_variant | 0.12 |
rpoB | 761539 | p.Arg578Leu | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763530 | p.Pro54Arg | missense_variant | 0.11 |
rpoC | 764038 | p.Trp223Cys | missense_variant | 0.12 |
rpoC | 767071 | c.3702C>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775642 | p.Pro947Ala | missense_variant | 0.11 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777264 | p.Leu406Pro | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472912 | n.1067C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473354 | n.1509G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473592 | n.-65delA | upstream_gene_variant | 0.18 |
rrl | 1476175 | n.2518G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476367 | n.2710G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476787 | n.3130C>A | non_coding_transcript_exon_variant | 0.22 |
inhA | 1673718 | c.-484G>T | upstream_gene_variant | 0.15 |
inhA | 1674449 | p.Gly83Val | missense_variant | 0.12 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102267 | p.Val259Ala | missense_variant | 0.14 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2155708 | p.Trp135Ser | missense_variant | 0.1 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2169138 | p.Thr492Met | missense_variant | 0.11 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289925 | c.-684T>C | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518284 | p.Ala57Glu | missense_variant | 0.13 |
kasA | 2518511 | p.Gly133Ser | missense_variant | 0.17 |
eis | 2714571 | c.762G>A | synonymous_variant | 0.12 |
ahpC | 2726608 | p.Asp139Val | missense_variant | 0.12 |
folC | 2746474 | c.1125G>T | synonymous_variant | 0.12 |
folC | 2746523 | p.Ala359Glu | missense_variant | 0.12 |
Rv2752c | 3065556 | c.636G>T | synonymous_variant | 0.11 |
thyA | 3073880 | p.Glu198Lys | missense_variant | 0.12 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3449396 | p.Cys298Phe | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3474981 | c.975C>A | synonymous_variant | 0.12 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiA | 3640636 | p.Ser32Pro | missense_variant | 1.0 |
fbiB | 3641325 | c.-210G>A | upstream_gene_variant | 0.12 |
fbiB | 3642239 | c.705G>T | synonymous_variant | 0.14 |
fbiB | 3642478 | p.Asp315Ala | missense_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244556 | p.Arg442Gly | missense_variant | 0.1 |
embA | 4244711 | c.1479C>T | synonymous_variant | 0.15 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247163 | p.Leu217Pro | missense_variant | 0.11 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267373 | c.1464C>T | synonymous_variant | 0.12 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268535 | p.Gly101Val | missense_variant | 0.12 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |