Run ID: ERR2229065
Sample name:
Date: 31-03-2023 16:34:43
Number of reads: 696524
Percentage reads mapped: 99.52
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 | 0.22 |
ccsA | 620250 | c.360C>A | synonymous_variant | 0.12 |
ccsA | 620773 | p.Ile295Val | missense_variant | 0.2 |
rpoB | 759762 | c.-45T>A | upstream_gene_variant | 0.17 |
rpoB | 760847 | c.1041C>A | synonymous_variant | 0.15 |
rpoC | 765589 | c.2220G>T | synonymous_variant | 0.17 |
rpoC | 765823 | c.2456dupG | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775927 | c.2554C>T | synonymous_variant | 0.13 |
mmpL5 | 775931 | c.2550C>T | synonymous_variant | 0.14 |
mmpL5 | 777486 | p.Phe332Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303331 | p.Arg134Leu | missense_variant | 0.22 |
fbiC | 1303396 | p.Arg156Cys | missense_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304869 | p.Leu647Met | missense_variant | 0.2 |
atpE | 1460983 | c.-62A>T | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474079 | n.423delA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475430 | n.1773T>C | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.14 |
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 | 0.4 |
inhA | 1673526 | c.-676G>A | upstream_gene_variant | 0.15 |
inhA | 1674754 | p.Arg185Ser | missense_variant | 0.22 |
rpsA | 1833643 | c.102C>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101727 | p.Arg439Leu | missense_variant | 0.18 |
PPE35 | 2167746 | p.Thr956Phe | missense_variant | 0.13 |
PPE35 | 2168160 | p.Glu818Val | missense_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2222581 | p.Thr195Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518619 | p.Ser169Pro | missense_variant | 0.15 |
kasA | 2518806 | p.Asp231Val | missense_variant | 0.12 |
Rv2752c | 3064760 | p.Val478Met | missense_variant | 0.12 |
Rv2752c | 3066107 | p.Arg29Cys | missense_variant | 0.12 |
thyA | 3073843 | p.Asp210Gly | missense_variant | 0.12 |
panD | 4044182 | p.Asp34Tyr | missense_variant | 0.17 |
embC | 4242375 | p.Arg838Gln | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243854 | p.Leu208Phe | missense_variant | 0.12 |
embB | 4246686 | p.Trp58* | stop_gained | 0.25 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.21 |
embB | 4249170 | p.Asn886Ser | missense_variant | 0.17 |
embB | 4249173 | p.Ser887Asn | missense_variant | 0.17 |
aftB | 4267476 | p.Ser454Leu | missense_variant | 0.15 |
aftB | 4268776 | p.Ser21Gly | missense_variant | 0.12 |
ethA | 4326924 | p.Gly184Ser | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408330 | c.-128G>T | upstream_gene_variant | 0.13 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |