Run ID: SRR15296920
Sample name:
Date: 03-04-2023 12:42:09
Number of reads: 401256
Percentage reads mapped: 99.16
Strain: La1.7.1
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
pncA | 2288682 | c.559_560insA | frameshift_variant&splice_region_variant | 1.0 | pyrazinamide |
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 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.15 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.33 |
rpoB | 761129 | c.1323G>A | synonymous_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1304948 | p.Asp673Gly | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917954 | c.15C>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.92 |
katG | 2154984 | c.1128G>A | synonymous_variant | 0.93 |
katG | 2155468 | p.Asp215Gly | missense_variant | 0.12 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
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 | 2170004 | c.609C>T | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.31 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288921 | p.Glu107Asp | missense_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726529 | p.Asp113Asn | missense_variant | 0.4 |
pepQ | 2859693 | c.726C>T | synonymous_variant | 1.0 |
pepQ | 2860178 | p.Arg81Ser | missense_variant | 1.0 |
ribD | 2987071 | p.Ala78Val | missense_variant | 0.11 |
Rv2752c | 3065475 | c.717C>T | synonymous_variant | 0.22 |
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 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3641958 | p.Val142Ile | missense_variant | 0.88 |
fbiB | 3642121 | p.Asp196Val | missense_variant | 0.12 |
fbiB | 3642204 | p.Asp224Asn | missense_variant | 0.2 |
fbiB | 3642478 | p.Asp315Ala | missense_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038605 | p.Glu700Asp | missense_variant | 0.13 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.33 |
embC | 4240080 | p.Pro73Gln | missense_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 | 4244666 | c.1434G>C | synonymous_variant | 0.22 |
embA | 4244721 | p.Gln497* | stop_gained | 0.22 |
embA | 4245603 | p.Gly791Arg | missense_variant | 0.12 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247276 | p.Pro255Ser | missense_variant | 0.12 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248833 | p.Trp774Arg | missense_variant | 0.18 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
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 |
ethR | 4328045 | p.Leu166Pro | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |