Run ID: ERR2229296
Sample name:
Date: 31-03-2023 16:58:19
Number of reads: 1090070
Percentage reads mapped: 99.14
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 | 575298 | c.-50T>A | upstream_gene_variant | 0.4 |
mshA | 575336 | c.-12G>T | upstream_gene_variant | 0.29 |
rpoC | 764284 | c.915G>A | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.15 |
mmpL5 | 777914 | c.567G>T | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416927 | p.Ala141Ser | missense_variant | 0.15 |
embR | 1416963 | p.Gly129Cys | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475059 | n.1402G>C | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.19 |
rpsA | 1834809 | p.Arg423Leu | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918588 | p.Glu217* | stop_gained | 0.2 |
ndh | 2103076 | c.-34C>A | upstream_gene_variant | 0.11 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.21 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.22 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.19 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.28 |
PPE35 | 2170528 | p.Ser29Ala | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.18 |
kasA | 2519171 | p.Leu353Val | missense_variant | 0.18 |
folC | 2746548 | p.Asp351Asn | missense_variant | 0.15 |
pepQ | 2860617 | c.-199C>T | upstream_gene_variant | 0.12 |
ald | 3087896 | c.1077G>C | synonymous_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.39 |
rpoA | 3877859 | p.Glu217* | stop_gained | 0.17 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.13 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.27 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242799 | c.-434T>C | upstream_gene_variant | 0.11 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.33 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.36 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.3 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.22 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.15 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.14 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.14 |
ubiA | 4269575 | p.Lys87Glu | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |