Run ID: ERR4627311
Sample name:
Date: 01-04-2023 06:30:49
Number of reads: 1108981
Percentage reads mapped: 65.71
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 | 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 | 1.0 |
mshA | 576410 | p.Phe355Leu | missense_variant | 0.1 |
mshA | 576446 | p.Thr367Pro | missense_variant | 0.25 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.25 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.14 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.11 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.12 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.12 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.12 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.12 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763101 | p.Ala1099Thr | missense_variant | 0.12 |
rpoB | 763151 | p.Phe1115Leu | missense_variant | 0.17 |
rpoC | 764535 | p.Arg389Pro | missense_variant | 0.17 |
rpoC | 765297 | p.Pro643Leu | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777305 | c.1176C>A | synonymous_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801114 | c.306C>G | synonymous_variant | 0.12 |
rplC | 801454 | p.Glu216Gln | missense_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305047 | p.Ser706* | stop_gained | 0.22 |
Rv1258c | 1407175 | c.166T>C | synonymous_variant | 0.12 |
Rv1258c | 1407220 | c.118_120delAGC | conservative_inframe_deletion | 0.11 |
embR | 1416527 | p.Val274Ala | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476405 | n.2748C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476473 | n.2816G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476492 | n.2835G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476561 | n.2904C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476728 | n.3071T>A | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.23 |
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 |
tlyA | 1918052 | p.Pro38Arg | missense_variant | 0.18 |
tlyA | 1918618 | p.Ala227Pro | missense_variant | 0.16 |
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 | 2168265 | p.Gly783Val | missense_variant | 0.12 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2170024 | p.Thr197Ser | 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 | 2518512 | c.403delC | frameshift_variant | 0.2 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.2 |
thyX | 3067311 | c.634delG | frameshift_variant | 0.12 |
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 | 3339734 | p.Ala206Gly | missense_variant | 0.33 |
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 |
alr | 3841069 | p.Ile118Val | missense_variant | 0.1 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039566 | p.Val380Gly | missense_variant | 0.15 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.25 |
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 | 4243251 | p.Glu7Lys | missense_variant | 0.12 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.25 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4246949 | c.438delA | frameshift_variant | 0.11 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.33 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.4 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.67 |
embB | 4247484 | p.Gly324Val | missense_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248734 | p.Arg741Trp | missense_variant | 1.0 |
embB | 4249527 | p.Gly1005Val | missense_variant | 0.15 |
aftB | 4267167 | p.Gln557Pro | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268453 | c.384G>T | synonymous_variant | 0.14 |
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 |