Run ID: SRR5382721
Sample name:
Date: 04-04-2023 10:23:43
Number of reads: 4673170
Percentage reads mapped: 68.03
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 | 0.99 |
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 | 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 |
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 | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472349 | n.504A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472374 | n.529T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472390 | n.545T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472398 | n.553T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473162 | n.1317C>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474828 | n.1171G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474832 | n.1176delG | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.23 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_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 | 2170048 | p.Leu189Val | missense_variant | 0.19 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>A | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | 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 |
fbiB | 3641590 | p.Gly19Glu | missense_variant | 0.98 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 0.9 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.98 |
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 | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 0.97 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.98 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |