Run ID: ERR2747605
Sample name:
Date: 31-03-2023 23:28:00
Number of reads: 650157
Percentage reads mapped: 80.54
Strain: La1.8.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
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 | 6927 | p.Leu563* | stop_gained | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7541 | c.240C>A | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7655 | c.354G>C | synonymous_variant | 0.18 |
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 | 490659 | c.-124G>T | upstream_gene_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575504 | p.His53Tyr | missense_variant | 0.14 |
mshA | 575961 | p.Gln205Arg | missense_variant | 0.12 |
mshA | 576009 | p.Ala221Val | missense_variant | 0.13 |
mshA | 576122 | p.Leu259Ile | missense_variant | 0.14 |
rpoB | 759651 | c.-156A>T | upstream_gene_variant | 0.4 |
rpoB | 759970 | p.Phe55Tyr | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763277 | c.-93A>T | upstream_gene_variant | 0.4 |
rpoC | 767178 | p.Ile1270Asn | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778993 | p.Ser2Gly | missense_variant | 0.22 |
mmpL5 | 779325 | c.-845G>A | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801040 | p.Arg78Cys | missense_variant | 0.17 |
rplC | 801454 | p.Glu216Gln | missense_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303262 | p.Pro111Leu | missense_variant | 0.14 |
fbiC | 1304223 | c.1293G>T | synonymous_variant | 0.33 |
fbiC | 1304866 | p.Gly646Arg | missense_variant | 0.4 |
fbiC | 1305455 | p.Arg842His | missense_variant | 0.15 |
Rv1258c | 1406234 | c.1106delC | frameshift_variant | 0.29 |
Rv1258c | 1406861 | c.480C>A | synonymous_variant | 0.15 |
Rv1258c | 1407310 | p.Leu11Met | missense_variant | 0.12 |
atpE | 1460849 | c.-196G>A | upstream_gene_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673715 | c.-487C>G | upstream_gene_variant | 1.0 |
inhA | 1674834 | c.633C>T | synonymous_variant | 0.22 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918668 | c.729G>A | synonymous_variant | 0.18 |
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 | 2169491 | c.1122T>C | synonymous_variant | 0.38 |
PPE35 | 2170563 | p.Ala17Val | missense_variant | 0.18 |
Rv1979c | 2222200 | p.Gly322Asp | missense_variant | 0.33 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222585 | p.Ala194Thr | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290028 | c.-787C>T | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
Rv2752c | 3066128 | p.Gly22Ser | missense_variant | 0.25 |
Rv2752c | 3066146 | c.46T>C | synonymous_variant | 0.22 |
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 |
ald | 3087461 | c.642G>T | synonymous_variant | 0.22 |
fbiD | 3339713 | p.Arg199His | missense_variant | 0.14 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475026 | c.1020C>T | synonymous_variant | 0.13 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3642551 | p.Gln339His | missense_variant | 0.12 |
fbiB | 3642809 | c.1275G>A | synonymous_variant | 0.22 |
alr | 3840785 | c.636C>T | synonymous_variant | 0.14 |
alr | 3841204 | p.Gly73Cys | missense_variant | 0.15 |
rpoA | 3877941 | c.567C>T | synonymous_variant | 0.2 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4040833 | c.-129G>T | upstream_gene_variant | 0.15 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241254 | c.1392C>T | synonymous_variant | 0.25 |
embC | 4241426 | c.1564C>T | synonymous_variant | 0.18 |
embC | 4242642 | p.Arg927His | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243487 | p.Asn85Lys | missense_variant | 0.15 |
embA | 4244041 | p.Thr270Asn | missense_variant | 0.17 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244854 | p.Val541Glu | missense_variant | 0.22 |
embA | 4245280 | p.Arg683His | missense_variant | 0.2 |
embA | 4245373 | p.Pro714Arg | missense_variant | 0.17 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247309 | p.Arg266Cys | missense_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248734 | p.Arg741Trp | missense_variant | 1.0 |
embB | 4249120 | c.2607C>T | synonymous_variant | 0.22 |
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 |
ubiA | 4269614 | p.Asp74His | missense_variant | 0.2 |
ethA | 4326006 | c.1468T>G | stop_lost&splice_region_variant | 0.4 |
ethA | 4326024 | p.Pro484Ser | missense_variant | 1.0 |
ethA | 4326152 | p.Arg441His | missense_variant | 0.22 |
ethA | 4328213 | c.-740C>T | upstream_gene_variant | 0.15 |
whiB6 | 4338564 | c.-43C>T | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408375 | c.-173G>T | upstream_gene_variant | 0.33 |