Run ID: ERR4820424
Sample name:
Date: 01-04-2023 16:40:45
Number of reads: 5609800
Percentage reads mapped: 97.7
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.66 | streptomycin |
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 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 778800 | p.Gly36Ser | missense_variant | 1.0 |
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 | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474321 | n.664T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475620 | n.1963T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475794 | n.2137A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_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 | 0.98 |
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 | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
pepQ | 2859754 | p.Phe222Ser | 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 |
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 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
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 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 0.99 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
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 |
ethA | 4327530 | c.-57G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |