Run ID: ERR2245283
Sample name:
Date: 31-03-2023 17:37:14
Number of reads: 1172222
Percentage reads mapped: 99.42
Strain: lineage3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6937 | c.-365G>A | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7649 | p.Phe116Leu | missense_variant | 0.12 |
gyrA | 7946 | c.645C>A | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491405 | p.Met208Lys | missense_variant | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763743 | p.Leu125Gln | missense_variant | 0.13 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.12 |
rpoC | 766796 | p.Arg1143Cys | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777259 | p.Leu408Met | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303545 | p.Lys205Asn | missense_variant | 0.11 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.36 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674435 | c.234G>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102676 | c.363_366dupTGGC | frameshift_variant | 0.14 |
ndh | 2102825 | p.Arg73Leu | missense_variant | 0.12 |
katG | 2154032 | p.Val694Met | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169049 | p.Ile522Phe | missense_variant | 0.17 |
PPE35 | 2169056 | c.1557A>T | synonymous_variant | 0.18 |
PPE35 | 2169214 | p.Ile467Val | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.25 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2222500 | p.Ala222Val | missense_variant | 0.15 |
Rv1979c | 2222776 | p.Ala130Asp | missense_variant | 0.25 |
Rv1979c | 2223036 | c.129A>G | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.13 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.14 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3065523 | p.His223Gln | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449372 | p.Tyr290Phe | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612078 | p.Ser347Ala | missense_variant | 0.18 |
Rv3236c | 3612218 | p.Val300Gly | missense_variant | 0.2 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.55 |
clpC1 | 4038558 | p.Ile716Asn | missense_variant | 0.12 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244355 | p.Phe375Leu | missense_variant | 0.18 |
embA | 4244358 | p.Asn376Asp | missense_variant | 0.2 |
embA | 4244976 | p.Gly582Trp | missense_variant | 0.12 |
embA | 4245438 | p.Ala736Ser | missense_variant | 0.17 |
embB | 4247023 | c.510G>A | synonymous_variant | 0.13 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.25 |
ethR | 4328110 | p.Ala188Ser | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408220 | c.-18G>A | upstream_gene_variant | 0.13 |