Run ID: SRR18391723
Sample name:
Date: 03-04-2023 19:41:14
Number of reads: 200331
Percentage reads mapped: 65.06
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 | 6585 | p.Asp449Gly | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7761 | p.Pro154Thr | missense_variant | 0.14 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8951 | p.Lys550Asn | missense_variant | 0.15 |
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 |
mshA | 575390 | p.Gln15Lys | missense_variant | 0.2 |
mshA | 575410 | c.63C>G | synonymous_variant | 0.22 |
mshA | 575910 | p.Leu188Gln | missense_variant | 0.67 |
mshA | 576239 | p.Ala298Thr | missense_variant | 0.25 |
ccsA | 619999 | p.Ala37Ser | missense_variant | 0.67 |
ccsA | 620128 | p.Gly80Trp | missense_variant | 0.29 |
rpoB | 761381 | c.1575G>A | synonymous_variant | 0.22 |
rpoB | 762159 | p.Arg785Cys | missense_variant | 0.22 |
rpoB | 762444 | p.Ala880Thr | missense_variant | 0.22 |
rpoC | 762590 | c.-780C>A | upstream_gene_variant | 0.25 |
rpoC | 762776 | c.-594C>A | upstream_gene_variant | 0.4 |
rpoB | 762861 | p.Val1019Ile | missense_variant | 0.33 |
rpoC | 762887 | c.-483G>A | upstream_gene_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764757 | p.Leu463Pro | missense_variant | 0.12 |
rpoC | 766129 | c.2760C>A | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775811 | p.Phe890Leu | missense_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776378 | p.Phe701Leu | missense_variant | 0.2 |
mmpL5 | 776745 | p.Arg579Leu | missense_variant | 0.2 |
mmpL5 | 777529 | p.Ala318Thr | missense_variant | 0.22 |
mmpL5 | 778366 | p.Trp39Gly | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801079 | p.Ala91Thr | missense_variant | 0.15 |
rplC | 801415 | p.Gly203Arg | missense_variant | 0.4 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305149 | p.Val740Asp | missense_variant | 0.18 |
Rv1258c | 1406474 | c.867G>A | synonymous_variant | 0.2 |
embR | 1416201 | p.Gly383Trp | missense_variant | 0.15 |
embR | 1416468 | p.Asp294Tyr | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472055 | n.210C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472117 | n.272A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472856 | n.1011T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472923 | n.1078G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472934 | n.1089C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474566 | n.909G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475208 | n.1551C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475573 | n.1916G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475631 | n.1974G>T | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673552 | c.114_115delCG | frameshift_variant | 0.18 |
inhA | 1674503 | p.Thr101Ile | missense_variant | 0.29 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918122 | c.183C>T | synonymous_variant | 0.25 |
ndh | 2101992 | p.Leu351Met | missense_variant | 0.12 |
ndh | 2102754 | p.Gln97Lys | missense_variant | 0.29 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155104 | c.1008G>A | synonymous_variant | 0.18 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167878 | p.Ser912Asn | missense_variant | 0.5 |
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 | 2169249 | p.Ile455Thr | missense_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222973 | c.192C>A | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289272 | c.-31C>T | upstream_gene_variant | 0.2 |
kasA | 2518024 | c.-91C>A | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518716 | p.Pro201His | missense_variant | 0.29 |
eis | 2714608 | p.Arg242Met | missense_variant | 0.22 |
eis | 2714863 | p.Gly157Val | missense_variant | 0.5 |
eis | 2715218 | p.Leu39Met | missense_variant | 0.18 |
ahpC | 2726023 | c.-170T>C | upstream_gene_variant | 0.33 |
folC | 2746373 | p.Pro409Gln | missense_variant | 0.22 |
ribD | 2987495 | c.657C>T | synonymous_variant | 0.25 |
thyX | 3067861 | p.Ala29Ser | missense_variant | 0.18 |
thyA | 3074225 | p.Trp83Arg | 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 |
ald | 3087776 | c.957G>A | synonymous_variant | 0.14 |
fbiD | 3338925 | c.-193G>A | upstream_gene_variant | 0.29 |
fbiD | 3339740 | p.Ala208Val | missense_variant | 0.17 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3448926 | c.423C>A | synonymous_variant | 0.15 |
Rv3083 | 3449163 | c.660G>A | synonymous_variant | 0.2 |
Rv3083 | 3449673 | c.1170C>T | synonymous_variant | 0.2 |
Rv3083 | 3449882 | p.Trp460Leu | missense_variant | 0.25 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 0.67 |
fprA | 3474350 | p.Pro115His | missense_variant | 0.4 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475020 | c.1014C>T | synonymous_variant | 0.4 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568435 | p.Pro82Gln | missense_variant | 0.25 |
whiB7 | 3568442 | p.Lys80Glu | missense_variant | 0.22 |
fbiA | 3640636 | p.Ser32Pro | missense_variant | 1.0 |
fbiB | 3642135 | p.Ala201Pro | missense_variant | 0.18 |
fbiB | 3642170 | c.636G>A | synonymous_variant | 0.18 |
fbiB | 3642478 | p.Asp315Ala | missense_variant | 1.0 |
alr | 3840849 | p.Arg191Leu | missense_variant | 0.22 |
alr | 3841178 | c.243C>A | synonymous_variant | 0.18 |
alr | 3841492 | c.-72C>T | upstream_gene_variant | 0.15 |
rpoA | 3877496 | p.Glu338Gln | missense_variant | 0.25 |
rpoA | 3877754 | p.Asp252Asn | missense_variant | 0.2 |
rpoA | 3877899 | c.609C>T | synonymous_variant | 0.2 |
rpoA | 3878536 | c.-29G>T | upstream_gene_variant | 0.5 |
ddn | 3987251 | p.Tyr136* | stop_gained | 0.29 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038947 | c.1758C>T | synonymous_variant | 0.4 |
clpC1 | 4039112 | c.1593C>T | synonymous_variant | 0.12 |
embC | 4240201 | c.339G>A | synonymous_variant | 0.25 |
embC | 4240458 | p.Gly199Val | missense_variant | 0.4 |
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 | 4243184 | c.-49G>A | upstream_gene_variant | 0.2 |
embA | 4243928 | c.696C>A | synonymous_variant | 0.33 |
embA | 4243958 | c.726G>A | synonymous_variant | 0.4 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4245110 | p.Tyr626* | stop_gained | 0.33 |
embB | 4246370 | c.-144G>T | upstream_gene_variant | 0.18 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246745 | p.Asp78Tyr | missense_variant | 0.5 |
embB | 4246772 | p.Val87Met | missense_variant | 0.5 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247810 | p.Leu433Val | missense_variant | 0.29 |
aftB | 4267009 | p.Leu610Met | missense_variant | 0.17 |
aftB | 4267591 | p.Gln416Lys | missense_variant | 0.22 |
aftB | 4267611 | p.Asp409Gly | missense_variant | 0.2 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268506 | c.331C>A | synonymous_variant | 0.5 |
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 | 4328177 | p.Ser210Ile | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408422 | c.-220T>C | upstream_gene_variant | 0.25 |