Run ID: ERR245817
Sample name:
Date: 31-03-2023 18:22:48
Number of reads: 1693985
Percentage reads mapped: 98.96
Strain: lineage1.1.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.99 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
lineage1.1.3.2 | Indo-Oceanic | NA | RD239 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8188 | p.Leu296Pro | missense_variant | 0.96 |
gyrA | 8445 | p.Arg382Gly | missense_variant | 0.22 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9174 | c.1873C>T | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.99 |
ccsA | 619695 | c.-196G>A | upstream_gene_variant | 1.0 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.24 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.21 |
rpoB | 762249 | p.Leu815Val | missense_variant | 0.19 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.36 |
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 | 764725 | p.Phe452Leu | missense_variant | 0.4 |
rpoC | 764905 | p.Phe512Leu | missense_variant | 0.13 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
rpoC | 767305 | p.Tyr1312* | stop_gained | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.64 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781900 | p.Arg114Pro | missense_variant | 0.2 |
rplC | 801166 | p.Gly120Ser | missense_variant | 1.0 |
fbiC | 1303901 | p.Val324Gly | missense_variant | 0.4 |
Rv1258c | 1407522 | c.-182C>G | upstream_gene_variant | 0.4 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417136 | p.Ser71Ile | missense_variant | 0.4 |
embR | 1417233 | c.115C>T | synonymous_variant | 0.28 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473360 | n.1515T>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.16 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.18 |
inhA | 1674883 | p.Ile228Val | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.23 |
katG | 2154615 | c.1497G>C | synonymous_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.98 |
katG | 2154758 | p.Glu452Lys | missense_variant | 0.19 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.99 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.98 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.44 |
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 | 1.0 |
kasA | 2518891 | c.777C>A | synonymous_variant | 0.22 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.31 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.55 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.98 |
ahpC | 2726756 | c.564C>G | synonymous_variant | 0.24 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.4 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.25 |
pepQ | 2859680 | p.Leu247Val | missense_variant | 0.33 |
ribD | 2987392 | p.Arg185Pro | missense_variant | 0.15 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.42 |
thyX | 3067965 | c.-20C>G | upstream_gene_variant | 0.38 |
thyA | 3073800 | c.672G>C | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448929 | p.Tyr142* | stop_gained | 0.25 |
Rv3083 | 3449058 | p.Ser185Arg | missense_variant | 0.64 |
Rv3083 | 3449673 | p.Tyr390* | stop_gained | 0.34 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474079 | p.Ala25Pro | missense_variant | 0.25 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475244 | p.Arg413Pro | missense_variant | 0.25 |
Rv3236c | 3612425 | p.Ala231Gly | missense_variant | 0.5 |
Rv3236c | 3612960 | p.Ala53Pro | missense_variant | 0.33 |
fbiB | 3641687 | p.Lys51Asn | missense_variant | 0.12 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.4 |
fbiB | 3642033 | p.Ala167Pro | missense_variant | 0.27 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 1.0 |
alr | 3841472 | c.-52C>G | upstream_gene_variant | 0.35 |
rpoA | 3877766 | p.Ala248Pro | missense_variant | 0.35 |
rpoA | 3878687 | c.-180A>C | upstream_gene_variant | 1.0 |
rpoA | 3878692 | c.-185C>G | upstream_gene_variant | 0.22 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.17 |
clpC1 | 4039363 | p.Ala448Pro | missense_variant | 0.17 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.29 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044406 | c.-125C>G | upstream_gene_variant | 0.27 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.67 |
embC | 4241128 | c.1266G>C | synonymous_variant | 0.2 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.43 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.5 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.33 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244375 | c.1143C>G | synonymous_variant | 0.33 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.47 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.38 |
ethR | 4328138 | p.Ala197Gly | missense_variant | 0.26 |
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 | 4407780 | c.423G>A | synonymous_variant | 0.95 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.96 |
gid | 4408273 | c.-71C>G | upstream_gene_variant | 0.21 |