Run ID: ERR3439229
Sample name:
Date: 01-04-2023 01:58:12
Number of reads: 863172
Percentage reads mapped: 69.12
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 |
gyrB | 5789 | p.Glu184Lys | missense_variant | 0.13 |
gyrB | 5934 | p.Ser232* | stop_gained | 0.18 |
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 | 8048 | c.747C>A | synonymous_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 | 0.94 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776032 | p.Gly817Arg | missense_variant | 0.23 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778327 | p.Gln52Lys | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801454 | p.Glu216Gln | missense_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303380 | c.450T>C | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474768 | n.1111C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474801 | n.1144G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474826 | n.1169T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475752 | n.2095C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475776 | n.2119G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.5 |
inhA | 1673715 | c.-487C>G | upstream_gene_variant | 1.0 |
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 | 2154085 | p.Gly676Val | missense_variant | 0.22 |
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 | 2169689 | c.924C>T | synonymous_variant | 0.18 |
PPE35 | 2170678 | c.-66C>A | upstream_gene_variant | 0.13 |
Rv1979c | 2221893 | c.1272C>A | synonymous_variant | 0.25 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222354 | p.Leu271Ile | missense_variant | 0.2 |
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 |
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 |
clpC1 | 4039927 | p.Arg260Ser | missense_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4242642 | p.Arg927His | 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 | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248734 | p.Arg741Trp | missense_variant | 1.0 |
aftB | 4267167 | p.Gln557Pro | 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 | 4326024 | p.Pro484Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |