Run ID: ERR2229478
Sample name:
Date: 31-03-2023 17:14:05
Number of reads: 616459
Percentage reads mapped: 99.43
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326880 | c.593delG | frameshift_variant | 0.18 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5874 | p.Arg212Thr | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.3 |
mshA | 576173 | p.Pro276Ser | missense_variant | 0.33 |
ccsA | 620543 | p.Arg218Gln | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781679 | c.120C>T | synonymous_variant | 0.14 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406174 | p.Cys389Trp | missense_variant | 0.2 |
atpE | 1460917 | c.-128C>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473466 | n.-192G>C | upstream_gene_variant | 0.11 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475914 | n.2257C>A | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.14 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.29 |
fabG1 | 1673884 | p.Asn149Asp | missense_variant | 0.11 |
rpsA | 1834698 | p.Glu386Gly | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102604 | c.439T>C | synonymous_variant | 0.21 |
ndh | 2102610 | c.433T>C | synonymous_variant | 0.2 |
katG | 2154232 | p.Leu627Gln | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.21 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2223159 | c.6C>T | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289319 | c.-78C>A | upstream_gene_variant | 0.12 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.22 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.17 |
kasA | 2519193 | p.Leu360Arg | missense_variant | 0.29 |
ahpC | 2725938 | c.-255_-254insA | upstream_gene_variant | 0.15 |
ribD | 2986677 | c.-162G>T | upstream_gene_variant | 0.12 |
ribD | 2986934 | c.96C>T | synonymous_variant | 0.2 |
Rv2752c | 3065539 | p.Val218Ala | missense_variant | 0.11 |
Rv2752c | 3067154 | c.-963G>T | upstream_gene_variant | 0.11 |
thyX | 3067610 | p.Lys112Asn | missense_variant | 0.17 |
ald | 3087139 | p.Leu107Ser | missense_variant | 0.12 |
fprA | 3473901 | c.-106G>A | upstream_gene_variant | 0.13 |
fprA | 3473920 | c.-87G>T | upstream_gene_variant | 0.13 |
fprA | 3474007 | c.1A>C | initiator_codon_variant | 0.17 |
fprA | 3475012 | p.Asp336Asn | missense_variant | 0.14 |
fbiB | 3641712 | p.Leu60Val | missense_variant | 0.15 |
fbiB | 3642422 | c.888A>T | synonymous_variant | 0.25 |
ddn | 3987201 | p.Ala120Thr | missense_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.31 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.13 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.14 |
embB | 4247915 | p.Arg468Cys | missense_variant | 0.15 |
embB | 4248138 | p.Gly542Asp | missense_variant | 0.11 |
embB | 4248586 | c.2073C>A | synonymous_variant | 0.13 |
embB | 4248686 | p.Gly725Trp | missense_variant | 0.2 |
embB | 4249346 | p.Ala945Thr | missense_variant | 0.18 |
aftB | 4267671 | p.Ala389Val | missense_variant | 0.12 |
aftB | 4268788 | p.Phe17Ile | missense_variant | 0.29 |
ethR | 4327571 | p.Gln8Leu | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407913 | p.Arg97His | missense_variant | 0.14 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |