Run ID: ERR245813
Sample name:
Date: 31-03-2023 18:23:06
Number of reads: 11226492
Percentage reads mapped: 99.14
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.99 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrB | 7158 | c.1931_1933delCCG | disruptive_inframe_deletion | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8150 | p.Phe283Leu | missense_variant | 1.0 |
gyrA | 8445 | p.Arg382Gly | missense_variant | 0.29 |
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 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.29 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.28 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304161 | p.Arg411Trp | missense_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.99 |
embR | 1417501 | c.-154A>C | upstream_gene_variant | 0.29 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.23 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.19 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.47 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918069 | p.Thr44Pro | missense_variant | 0.42 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.16 |
PPE35 | 2169379 | p.Phe412Val | missense_variant | 0.23 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.34 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.99 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.27 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.61 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.27 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726756 | c.564C>G | synonymous_variant | 0.28 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.97 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.28 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.17 |
thyA | 3073817 | p.Gln219Glu | missense_variant | 0.27 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339550 | p.Gly145Trp | missense_variant | 0.21 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474700 | p.Gly232Ser | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.24 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.22 |
alr | 3841437 | c.-17G>T | upstream_gene_variant | 0.16 |
alr | 3841441 | c.-21C>A | upstream_gene_variant | 0.2 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.27 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.14 |
clpC1 | 4039363 | p.Ala448Pro | missense_variant | 0.43 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.32 |
clpC1 | 4040369 | c.336C>T | synonymous_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239921 | p.Arg20Leu | missense_variant | 0.99 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.44 |
embC | 4241456 | p.Ala532Pro | missense_variant | 0.42 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.17 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.23 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.44 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.23 |
embA | 4243848 | p.Val206Met | missense_variant | 0.99 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249618 | c.3105C>G | synonymous_variant | 0.2 |
embB | 4249673 | p.Ser1054Pro | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.29 |
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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407935 | p.Leu90Val | missense_variant | 1.0 |
gid | 4407944 | p.Gln87Glu | missense_variant | 0.99 |