Run ID: ERR2660518
Sample name:
Date: 31-03-2023 22:53:47
Number of reads: 275994
Percentage reads mapped: 99.41
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 5541 | p.Thr101Ile | missense_variant | 0.4 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
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 | 575482 | c.135C>A | synonymous_variant | 0.18 |
mshA | 575549 | p.Met68Leu | missense_variant | 0.15 |
rpoB | 760832 | c.1026G>A | synonymous_variant | 0.5 |
rpoB | 761643 | p.Val613Ile | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763552 | c.183C>T | synonymous_variant | 1.0 |
rpoC | 766259 | p.Ser964Pro | missense_variant | 0.33 |
rpoC | 766558 | p.Lys1063Asn | missense_variant | 0.13 |
rpoC | 766916 | p.Arg1183Ser | missense_variant | 0.12 |
rpoC | 766974 | p.Ala1202Asp | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777447 | p.Ile345Asn | missense_variant | 0.14 |
mmpS5 | 779625 | c.-720G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781848 | p.Ile97Phe | missense_variant | 0.18 |
rpsL | 781860 | p.Ser101Thr | missense_variant | 0.18 |
rplC | 801007 | p.Thr67Ala | missense_variant | 0.2 |
rplC | 801019 | p.Thr71Pro | missense_variant | 0.17 |
rplC | 801159 | c.351C>T | synonymous_variant | 0.15 |
fbiC | 1305248 | p.Ala773Val | missense_variant | 0.22 |
Rv1258c | 1407102 | p.Ala80Val | missense_variant | 0.17 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1461055 | p.Thr4Asn | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473858 | n.201A>G | non_coding_transcript_exon_variant | 0.22 |
inhA | 1674905 | p.Ala235Val | missense_variant | 0.4 |
rpsA | 1833349 | c.-193C>A | upstream_gene_variant | 0.18 |
rpsA | 1834085 | p.Asn182His | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918084 | p.Thr49Ala | missense_variant | 0.4 |
tlyA | 1918120 | p.Ala61Ser | missense_variant | 0.29 |
ndh | 2101791 | p.Thr418Ser | missense_variant | 0.13 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155346 | p.Ala256Ser | missense_variant | 0.29 |
katG | 2155924 | p.Asp63Val | missense_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168449 | p.Gln722Glu | missense_variant | 0.29 |
PPE35 | 2170772 | c.-160C>A | upstream_gene_variant | 0.17 |
PPE35 | 2170809 | c.-197C>T | upstream_gene_variant | 0.25 |
Rv1979c | 2221771 | p.Leu465Pro | missense_variant | 0.4 |
Rv1979c | 2222098 | p.Thr356Lys | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222623 | p.Gly181Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518240 | c.126C>T | synonymous_variant | 0.25 |
kasA | 2519057 | p.Thr315Ser | missense_variant | 0.15 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.15 |
kasA | 2519065 | c.951C>A | synonymous_variant | 0.18 |
kasA | 2519070 | p.Asp319Val | missense_variant | 0.18 |
eis | 2715003 | c.330T>C | synonymous_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747345 | p.Leu85Arg | missense_variant | 0.15 |
folC | 2747734 | c.-136C>T | upstream_gene_variant | 0.14 |
ribD | 2986678 | c.-161C>T | upstream_gene_variant | 0.25 |
Rv2752c | 3065515 | p.Ile226Thr | missense_variant | 0.5 |
thyX | 3067370 | p.Trp192Cys | missense_variant | 0.2 |
thyX | 3067535 | c.411C>T | synonymous_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087210 | p.Ala131Thr | missense_variant | 0.12 |
fbiD | 3339465 | c.348T>C | synonymous_variant | 0.2 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449600 | p.Gln366Arg | missense_variant | 0.15 |
Rv3083 | 3449877 | p.His458Gln | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474214 | p.Thr70Pro | missense_variant | 0.18 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568605 | c.75C>G | synonymous_variant | 0.25 |
Rv3236c | 3612317 | p.Arg267His | missense_variant | 1.0 |
fbiA | 3641461 | p.Pro307Ala | missense_variant | 0.29 |
fbiB | 3641748 | c.214C>A | synonymous_variant | 0.33 |
alr | 3841168 | p.Gly85Ser | missense_variant | 0.2 |
rpoA | 3877885 | p.Leu208Pro | missense_variant | 0.15 |
rpoA | 3878230 | p.Val93Asp | missense_variant | 0.2 |
ddn | 3986910 | p.Arg23Trp | missense_variant | 0.14 |
clpC1 | 4039702 | p.Asp335Asn | missense_variant | 0.15 |
clpC1 | 4040278 | p.Ser143Pro | missense_variant | 0.11 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 1.0 |
embC | 4239698 | c.-165T>A | upstream_gene_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241599 | p.Met579Ile | missense_variant | 0.4 |
embC | 4241909 | p.Ala683Thr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244508 | p.Leu426Val | missense_variant | 0.12 |
embA | 4244909 | c.1677C>T | synonymous_variant | 0.25 |
embA | 4245670 | p.Ala813Gly | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246979 | p.Gly156Cys | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249787 | p.Gly1092Ser | missense_variant | 0.29 |
aftB | 4267201 | p.Trp546Arg | missense_variant | 0.33 |
aftB | 4267960 | p.Val293Met | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408132 | p.Glu24Val | missense_variant | 0.29 |