Run ID: ERR386958
Sample name:
Date: 01-04-2023 03:36:19
Number of reads: 7124140
Percentage reads mapped: 99.43
Strain: lineage4.1.1;lineage1.2.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.48 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.48 |
lineage4.1 | Euro-American | T;X;H | None | 0.48 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.48 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 0.54 |
lineage1.2.1.1 | Indo-Oceanic | NA | RD239 | 0.47 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.48 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.52 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 0.47 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.55 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.47 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.5 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.57 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775746 | p.Met912Thr | missense_variant | 0.51 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.51 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303858 | p.Gly310* | stop_gained | 0.49 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.44 |
atpE | 1460853 | c.-192T>G | upstream_gene_variant | 0.57 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.46 |
katG | 2155144 | p.Asn323Ser | missense_variant | 0.36 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.61 |
PPE35 | 2168533 | p.Val694Leu | missense_variant | 0.46 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290129 | c.-888C>A | upstream_gene_variant | 0.51 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.46 |
kasA | 2519035 | c.921C>T | synonymous_variant | 0.48 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.54 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 0.53 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.44 |
Rv3083 | 3448835 | p.Ser111Ile | missense_variant | 0.51 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.5 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.48 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 0.58 |
fbiB | 3641412 | c.-123G>A | upstream_gene_variant | 0.52 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 0.48 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 0.61 |
rpoA | 3878601 | c.-95delG | upstream_gene_variant | 0.2 |
rpoA | 3878613 | c.-113_-107delCAACCCA | upstream_gene_variant | 0.14 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.57 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.49 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.53 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.42 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.61 |
embA | 4244420 | c.1188G>C | synonymous_variant | 0.5 |
embA | 4244610 | p.Ala460Thr | missense_variant | 0.46 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.55 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.45 |
embB | 4248515 | p.Val668Ile | missense_variant | 0.52 |
embB | 4249352 | c.2839C>A | synonymous_variant | 0.51 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.49 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.53 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.55 |
ethR | 4327360 | c.-189C>G | upstream_gene_variant | 0.49 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 0.56 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.55 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.55 |
gid | 4407781 | p.Ala141Glu | missense_variant | 0.49 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.49 |
gid | 4407995 | p.Ser70Arg | missense_variant | 0.54 |