Run ID: SRR11294527
Sample name:
Date: 02-04-2023 20:45:40
Number of reads: 177081
Percentage reads mapped: 99.41
Strain: La1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154359 | c.1752delT | frameshift_variant | 0.18 | isoniazid |
katG | 2154845 | c.1266delC | frameshift_variant | 0.14 | isoniazid |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5333 | p.Met32Val | missense_variant | 0.12 |
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrB | 6055 | c.816T>C | synonymous_variant | 0.11 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.57 |
ccsA | 620830 | p.Thr314Ala | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.14 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776728 | p.Phe585Leu | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1406408 | c.933G>A | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475847 | n.2190A>G | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673616 | c.-586A>G | upstream_gene_variant | 0.22 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154444 | c.1668A>G | synonymous_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154984 | c.1128G>A | synonymous_variant | 1.0 |
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 | 2169565 | p.Gly350Ser | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222942 | p.Asn75His | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289020 | c.222C>T | synonymous_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715212 | c.119_120dupTG | frameshift_variant | 0.2 |
ahpC | 2726104 | c.-89T>G | upstream_gene_variant | 1.0 |
ahpC | 2726149 | c.-44T>C | upstream_gene_variant | 0.13 |
pepQ | 2859693 | c.726C>T | synonymous_variant | 1.0 |
Rv2752c | 3065257 | p.Met312Thr | missense_variant | 0.29 |
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 |
ald | 3087576 | c.758delC | frameshift_variant | 0.18 |
ald | 3087618 | p.Ile267Val | missense_variant | 0.15 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3449060 | p.Gly186Asp | missense_variant | 0.33 |
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 | 3642478 | p.Asp315Ala | missense_variant | 1.0 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.14 |
rpoA | 3878214 | c.294C>A | synonymous_variant | 1.0 |
ddn | 3987296 | c.453C>A | synonymous_variant | 0.17 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038593 | p.His704Gln | missense_variant | 0.11 |
clpC1 | 4038810 | p.Gln632Arg | missense_variant | 0.18 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.2 |
clpC1 | 4040652 | p.Glu18Gly | missense_variant | 0.12 |
panD | 4044363 | c.-82T>C | upstream_gene_variant | 0.22 |
embC | 4239897 | p.Val12Ala | missense_variant | 0.2 |
embC | 4240080 | p.Pro73Gln | missense_variant | 1.0 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.25 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242833 | p.Phe991Leu | missense_variant | 0.18 |
embA | 4242862 | c.-371A>G | upstream_gene_variant | 0.18 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244774 | c.1542G>A | synonymous_variant | 0.67 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4246986 | p.Phe158Tyr | missense_variant | 0.29 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248646 | c.2133C>G | synonymous_variant | 0.33 |
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 |
ethA | 4326180 | p.Met432Val | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338700 | c.-179T>C | upstream_gene_variant | 0.1 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408102 | p.Gly34Glu | missense_variant | 1.0 |