Run ID: ERR2229242
Sample name:
Date: 31-03-2023 16:52:43
Number of reads: 1378982
Percentage reads mapped: 98.85
Strain: lineage4.8
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.38 |
ccsA | 620341 | p.Val151Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777140 | c.1341G>C | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472006 | n.161G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472175 | n.330G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472743 | n.898T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.16 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.17 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.24 |
inhA | 1674742 | p.Lys181Glu | missense_variant | 0.12 |
rpsA | 1834195 | c.654G>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102901 | p.His48Asn | missense_variant | 0.3 |
ndh | 2102987 | p.Ile19Thr | missense_variant | 0.18 |
ndh | 2103022 | c.21C>A | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.11 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.14 |
PPE35 | 2169956 | c.657T>C | synonymous_variant | 0.12 |
PPE35 | 2169964 | p.Leu217Val | missense_variant | 0.12 |
PPE35 | 2169974 | c.639T>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.43 |
Rv1979c | 2222571 | c.594G>A | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.12 |
pepQ | 2859417 | c.1002C>T | synonymous_variant | 0.12 |
Rv2752c | 3064530 | c.1662G>T | synonymous_variant | 0.2 |
thyX | 3067537 | p.Asp137Asn | missense_variant | 0.12 |
thyA | 3074458 | p.Glu5Gly | missense_variant | 0.15 |
ald | 3087115 | p.Ala99Val | missense_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244901 | p.Ala557Ser | missense_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.21 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.27 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.27 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.25 |
ubiA | 4269370 | p.Ser155Leu | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |