Run ID: ERR4772229
Sample name:
Date: 01-04-2023 06:45:54
Number of reads: 949650
Percentage reads mapped: 99.13
Strain: La1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.2 | M.bovis | None | None | 0.97 |
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 | 7171 | c.-131C>A | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7821 | c.520C>T | synonymous_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8592 | p.Gln431Glu | missense_variant | 0.12 |
gyrA | 8615 | p.Met438Ile | missense_variant | 0.13 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 8997 | c.1696T>C | synonymous_variant | 0.11 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575619 | p.Arg91Leu | missense_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.24 |
rpoB | 760048 | p.Glu81Val | missense_variant | 0.2 |
rpoB | 760353 | p.Glu183* | stop_gained | 0.14 |
rpoB | 760663 | p.Ala286Glu | missense_variant | 0.13 |
rpoB | 762210 | p.Pro802Thr | missense_variant | 0.15 |
rpoB | 762238 | p.Glu811Gly | missense_variant | 0.15 |
rpoB | 763020 | p.Ala1072Thr | missense_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766962 | p.Gly1198Asp | missense_variant | 0.2 |
rpoC | 767197 | p.Glu1276Asp | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776795 | c.1686C>A | synonymous_variant | 0.15 |
mmpL5 | 777404 | c.1077C>T | synonymous_variant | 0.12 |
mmpR5 | 779122 | p.Val45Leu | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781494 | c.-66G>A | upstream_gene_variant | 0.12 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1304696 | p.Trp589Leu | missense_variant | 0.12 |
fbiC | 1304955 | p.Glu675Asp | missense_variant | 0.18 |
fbiC | 1305498 | c.2568C>A | synonymous_variant | 0.13 |
Rv1258c | 1406242 | p.Ala367Ser | missense_variant | 0.13 |
Rv1258c | 1406521 | p.Gly274* | stop_gained | 0.12 |
Rv1258c | 1406693 | c.648G>T | synonymous_variant | 0.12 |
Rv1258c | 1407280 | p.Ala21Thr | missense_variant | 0.14 |
embR | 1416550 | c.798C>A | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
inhA | 1674557 | p.Gly119Asp | missense_variant | 0.18 |
rpsA | 1834851 | p.Ala437Asp | missense_variant | 0.2 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918713 | p.Asp258Glu | missense_variant | 0.13 |
ndh | 2101802 | p.Leu414Gln | missense_variant | 0.12 |
ndh | 2101890 | p.Val385Ile | missense_variant | 0.17 |
ndh | 2102106 | p.Gly313Arg | 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 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
katG | 2156478 | c.-367A>C | upstream_gene_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168261 | p.Phe784Leu | missense_variant | 0.12 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.13 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222918 | c.245_246dupCA | frameshift_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289884 | c.-643G>A | upstream_gene_variant | 0.14 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518945 | p.Met277Ile | missense_variant | 0.12 |
pepQ | 2860132 | p.Gly96Ala | missense_variant | 0.11 |
Rv2752c | 3065381 | p.Arg271Cys | missense_variant | 0.13 |
Rv2752c | 3065888 | p.Val102Ile | missense_variant | 1.0 |
thyX | 3067786 | p.Thr54Ala | 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 |
fbiD | 3339154 | p.Ile13Leu | missense_variant | 1.0 |
Rv3083 | 3448737 | c.234C>T | synonymous_variant | 0.12 |
Rv3083 | 3448745 | p.Ile81Ser | missense_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3448889 | p.Arg129Leu | missense_variant | 0.25 |
fprA | 3473891 | c.-116A>C | upstream_gene_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 | 3840355 | p.Asp356Asn | missense_variant | 0.22 |
clpC1 | 4038242 | c.2463C>T | synonymous_variant | 0.14 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038766 | p.Leu647Ile | missense_variant | 0.12 |
clpC1 | 4038858 | p.Arg616Leu | missense_variant | 0.13 |
clpC1 | 4040361 | p.Glu115Gly | missense_variant | 0.14 |
clpC1 | 4040877 | c.-173T>A | upstream_gene_variant | 0.12 |
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 |
embA | 4244790 | p.Ala520Thr | missense_variant | 0.18 |
embB | 4245524 | c.-990G>A | upstream_gene_variant | 0.14 |
embB | 4246551 | p.Asn13Ser | missense_variant | 0.94 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247173 | c.660G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249412 | p.Arg967Trp | missense_variant | 0.12 |
aftB | 4267129 | p.Ala570Ser | missense_variant | 0.18 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268476 | p.Gly121Trp | missense_variant | 0.14 |
aftB | 4268598 | p.Glu80Gly | missense_variant | 0.22 |
aftB | 4268602 | c.235C>T | synonymous_variant | 0.22 |
aftB | 4268851 | c.-15T>G | upstream_gene_variant | 0.2 |
aftB | 4268855 | c.-19G>A | upstream_gene_variant | 0.2 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269502 | p.Val111Ala | missense_variant | 0.13 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
aftB | 4269666 | c.-830G>T | upstream_gene_variant | 0.13 |
whiB6 | 4338259 | p.Arg88Leu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407743 | p.Arg154Trp | missense_variant | 1.0 |