Run ID: ERR4627321
Sample name:
Date: 01-04-2023 06:31:24
Number of reads: 1404187
Percentage reads mapped: 91.3
Strain: La1.8.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | 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 |
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 | 8741 | c.1440C>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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 767042 | p.Ser1225Ala | missense_variant | 0.11 |
rpoC | 767284 | c.3915C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776702 | c.1779C>T | synonymous_variant | 0.17 |
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 | 1473052 | n.1207G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473053 | n.1208T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473054 | n.1209C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474415 | n.758C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474730 | n.1073A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474860 | n.1203G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475089 | n.1432A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475183 | n.1526A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475750 | n.2093A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476667 | n.3010T>A | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.2 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 0.97 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
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 | 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 | 2168259 | p.Thr785Lys | missense_variant | 0.17 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170143 | p.Gly157Val | missense_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519117 | p.Ala335Pro | missense_variant | 0.12 |
kasA | 2519181 | p.Val356Ala | missense_variant | 0.11 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
Rv2752c | 3065988 | p.Glu68Asp | missense_variant | 1.0 |
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 | 3449285 | p.Trp261* | stop_gained | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474039 | c.33C>A | synonymous_variant | 0.12 |
fprA | 3474101 | p.Leu32Arg | missense_variant | 0.12 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568582 | p.Pro33Arg | missense_variant | 0.11 |
fbiA | 3640990 | p.Cys150Arg | missense_variant | 0.11 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 0.88 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
panD | 4043989 | p.Ala98Val | missense_variant | 0.12 |
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 |
embC | 4242981 | p.Met1040Thr | missense_variant | 1.0 |
embA | 4243210 | c.-22delG | upstream_gene_variant | 0.11 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244322 | p.Ala364Ser | missense_variant | 0.12 |
embB | 4245641 | c.-873C>T | upstream_gene_variant | 0.14 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.29 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
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 | 4327741 | p.Phe65Ile | missense_variant | 0.15 |
ethR | 4327777 | p.Asp77Asn | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |