Run ID: ERR4769566
Sample name:
Date: 01-04-2023 06:44:33
Number of reads: 592577
Percentage reads mapped: 99.36
Strain: La1.6
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.6 | 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 |
gyrA | 6940 | c.-362G>A | upstream_gene_variant | 0.14 |
gyrA | 7042 | c.-260C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7655 | c.354G>T | synonymous_variant | 0.15 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8637 | p.Leu446Met | missense_variant | 0.14 |
gyrA | 8694 | p.Leu465Met | missense_variant | 0.25 |
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 |
gyrA | 9484 | p.Ser728Leu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575293 | c.-55T>A | upstream_gene_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.16 |
ccsA | 620768 | p.Ala293Gly | missense_variant | 1.0 |
rpoB | 762320 | c.2514C>T | synonymous_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764176 | c.807C>T | synonymous_variant | 1.0 |
rpoC | 764191 | c.822C>A | synonymous_variant | 0.15 |
rpoC | 766694 | p.Gln1109Lys | missense_variant | 0.15 |
rpoC | 766861 | c.3492G>T | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776354 | c.2127C>A | synonymous_variant | 0.13 |
mmpL5 | 777326 | c.1155C>A | synonymous_variant | 0.18 |
mmpS5 | 778674 | p.Pro78Thr | missense_variant | 0.14 |
mmpR5 | 779058 | p.Met23Ile | missense_variant | 0.2 |
mmpR5 | 779115 | p.Trp42* | stop_gained | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781894 | p.Gln112Arg | missense_variant | 0.11 |
rplC | 800953 | p.Ala49Thr | missense_variant | 0.14 |
rplC | 801232 | p.Gln142* | stop_gained | 0.15 |
fbiC | 1302860 | c.-71G>A | upstream_gene_variant | 0.13 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303160 | p.Gly77Glu | missense_variant | 0.17 |
fbiC | 1304078 | p.Glu383Gly | missense_variant | 1.0 |
embR | 1417493 | c.-146T>A | upstream_gene_variant | 0.12 |
atpE | 1461192 | p.Phe50Ile | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472923 | n.1078G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474414 | n.757C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475083 | n.1426C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475996 | n.2339T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476022 | n.2365A>G | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673310 | c.-130T>C | upstream_gene_variant | 0.13 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918632 | c.693G>T | synonymous_variant | 0.2 |
ndh | 2101985 | p.Gly353Val | missense_variant | 0.14 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154369 | c.1743G>A | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167731 | p.Phe961Tyr | missense_variant | 0.14 |
PPE35 | 2167925 | p.Leu896Ser | missense_variant | 0.12 |
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 | 2169047 | p.Ile522Met | missense_variant | 0.17 |
PPE35 | 2169222 | p.Ser464Tyr | missense_variant | 0.15 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.12 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169444 | p.Gly390Asp | missense_variant | 0.12 |
PPE35 | 2169660 | p.Asn318Ile | missense_variant | 0.25 |
PPE35 | 2169946 | p.Gly223Arg | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223062 | p.Thr35Ala | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289871 | c.-630T>A | upstream_gene_variant | 0.22 |
pncA | 2289890 | c.-649C>T | upstream_gene_variant | 0.22 |
pncA | 2290018 | c.-777C>G | upstream_gene_variant | 0.12 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726733 | p.Gly181Cys | missense_variant | 0.15 |
folC | 2746245 | p.Ala452Thr | missense_variant | 1.0 |
folC | 2746604 | p.Ala332Asp | missense_variant | 0.17 |
folC | 2746867 | c.732G>A | synonymous_variant | 0.2 |
folC | 2747013 | p.Pro196Thr | missense_variant | 0.2 |
pepQ | 2860144 | p.Val92Gly | missense_variant | 0.33 |
ribD | 2987012 | c.174C>A | synonymous_variant | 0.14 |
ribD | 2987057 | c.219G>A | synonymous_variant | 0.13 |
ribD | 2987279 | c.441G>T | synonymous_variant | 0.2 |
ribD | 2987615 | c.777A>G | stop_lost&splice_region_variant | 1.0 |
Rv2752c | 3065385 | c.807C>T | synonymous_variant | 0.22 |
Rv2752c | 3067083 | c.-892C>A | upstream_gene_variant | 0.17 |
thyA | 3073992 | p.Ser160Arg | missense_variant | 0.17 |
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 | 3449289 | c.786C>A | synonymous_variant | 0.15 |
Rv3083 | 3449550 | c.1047C>T | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474382 | p.Val126Ile | missense_variant | 0.12 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3474738 | c.732C>A | synonymous_variant | 0.15 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568872 | c.-193C>A | upstream_gene_variant | 0.17 |
Rv3236c | 3612675 | p.Thr148Ser | missense_variant | 0.33 |
fbiB | 3642797 | p.Leu421Phe | missense_variant | 0.17 |
alr | 3841034 | p.Gln129His | missense_variant | 0.14 |
clpC1 | 4038284 | p.Trp807Cys | missense_variant | 0.22 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
panD | 4044029 | p.Val85Leu | missense_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241902 | p.His680Gln | missense_variant | 0.15 |
embA | 4242313 | c.-920C>A | upstream_gene_variant | 0.18 |
embC | 4242608 | p.Glu916* | stop_gained | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242737 | c.2878delC | frameshift_variant | 0.2 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243954 | p.Arg241Pro | missense_variant | 0.18 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4245603 | p.Gly791Trp | missense_variant | 0.17 |
embA | 4245781 | p.Ala850Asp | missense_variant | 0.22 |
embA | 4245786 | p.Ala852Ser | missense_variant | 0.22 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.5 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247791 | c.1278C>T | synonymous_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268879 | c.-43G>A | upstream_gene_variant | 0.18 |
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 | 4326867 | p.Thr203Ala | missense_variant | 0.12 |
ethR | 4327993 | p.Thr149Ala | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408207 | c.-5G>T | upstream_gene_variant | 0.12 |