Run ID: ERR4627376
Sample name:
Date: 01-04-2023 06:33:41
Number of reads: 1434497
Percentage reads mapped: 75.39
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 | 6544 | c.-758C>T | upstream_gene_variant | 0.12 |
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 | 0.88 |
gyrA | 9052 | p.Leu584Ser | missense_variant | 0.11 |
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 | 491523 | c.745delT | frameshift_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.11 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.11 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.94 |
rpoC | 764668 | c.1299C>A | synonymous_variant | 0.18 |
rpoC | 765460 | c.2093delA | frameshift_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776246 | c.2235C>A | synonymous_variant | 0.12 |
mmpL5 | 777709 | c.771delG | frameshift_variant | 0.11 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781402 | c.-158_-157insG | upstream_gene_variant | 0.15 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1407521 | c.-181C>T | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471877 | n.32A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471898 | n.53A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472758 | n.913T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473003 | n.1158G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474952 | n.1295A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475599 | n.1942A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475632 | n.1975C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476227 | n.2570C>A | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.14 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
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 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2168964 | p.Val550Ala | missense_variant | 0.29 |
PPE35 | 2169919 | p.Leu232Ile | missense_variant | 0.12 |
PPE35 | 2170035 | p.Val193Ala | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.58 |
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 |
eis | 2715062 | p.His91Tyr | missense_variant | 0.12 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
folC | 2746816 | c.783C>A | synonymous_variant | 0.29 |
ribD | 2986675 | c.-164T>C | upstream_gene_variant | 0.12 |
thyA | 3074481 | c.-11delG | upstream_gene_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 |
fbiD | 3339738 | c.621C>A | synonymous_variant | 0.4 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3448808 | p.Leu102Pro | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474393 | c.389delG | frameshift_variant | 0.18 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3613100 | p.Ala6Val | missense_variant | 0.2 |
Rv3236c | 3613224 | c.-108C>T | upstream_gene_variant | 0.33 |
rpoA | 3878476 | c.31delG | frameshift_variant | 0.5 |
ddn | 3987222 | p.Val127Leu | missense_variant | 0.12 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242680 | p.Ala940Ser | missense_variant | 1.0 |
embC | 4242795 | p.Ala978Val | missense_variant | 0.13 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4246294 | p.Trp1021Ser | missense_variant | 0.12 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248122 | p.Leu537Met | missense_variant | 0.2 |
aftB | 4266962 | c.1875G>A | synonymous_variant | 0.17 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268029 | p.Leu270Met | missense_variant | 0.13 |
ubiA | 4269294 | p.Met180Ile | missense_variant | 0.15 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269473 | p.Thr121Pro | missense_variant | 0.25 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 0.2 |
ubiA | 4269943 | c.-110T>C | upstream_gene_variant | 0.2 |
ethA | 4327530 | c.-57G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338666 | c.-145G>A | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |