Run ID: ERR2229376
Sample name:
Date: 31-03-2023 17:07:56
Number of reads: 928079
Percentage reads mapped: 98.89
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 |
---|---|---|---|---|---|
tlyA | 1918030 | c.92_95delAGGT | frameshift_variant | 0.15 | capreomycin |
tlyA | 1918048 | c.109_110insACCT | frameshift_variant | 0.17 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7365 | p.Gln22Lys | missense_variant | 0.13 |
fgd1 | 491431 | p.Ala217Ser | missense_variant | 0.5 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.6 |
mshA | 576527 | p.Glu394* | stop_gained | 0.25 |
mshA | 576620 | p.Ala425Ser | missense_variant | 0.18 |
ccsA | 620220 | p.Met110Ile | missense_variant | 0.14 |
ccsA | 620783 | p.Ala298Val | missense_variant | 0.12 |
ccsA | 620837 | p.Gly316Val | missense_variant | 0.17 |
rpoB | 760575 | p.Glu257Gln | missense_variant | 0.12 |
rpoB | 761890 | p.Val695Glu | missense_variant | 0.12 |
rpoB | 762541 | p.Asn912Ser | missense_variant | 0.22 |
rpoB | 762555 | p.Pro917Thr | missense_variant | 0.2 |
rpoC | 763841 | p.Glu158* | stop_gained | 0.2 |
rpoC | 764588 | p.Lys407Gln | missense_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.15 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406400 | p.Ile314Thr | missense_variant | 0.15 |
atpE | 1461116 | c.72C>A | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473617 | n.-41T>A | upstream_gene_variant | 0.27 |
rrl | 1473895 | n.238C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474837 | n.1182delC | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475376 | n.1719A>G | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.2 |
rpsA | 1833397 | c.-145G>A | upstream_gene_variant | 0.2 |
rpsA | 1834175 | c.634C>A | synonymous_variant | 0.14 |
rpsA | 1834212 | p.Ala224Glu | missense_variant | 0.14 |
rpsA | 1834645 | p.Asp368Glu | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918037 | p.Arg33Pro | missense_variant | 0.15 |
tlyA | 1918039 | p.Ile34Val | missense_variant | 0.15 |
tlyA | 1918044 | c.105C>T | synonymous_variant | 0.17 |
tlyA | 1918046 | p.Gly36Ala | missense_variant | 0.17 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169027 | p.Leu529* | stop_gained | 0.18 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.19 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.2 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.21 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.69 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.7 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.16 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.14 |
Rv1979c | 2222785 | p.Trp127Leu | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289963 | c.-722A>G | upstream_gene_variant | 0.13 |
kasA | 2518525 | c.411G>T | synonymous_variant | 0.2 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.2 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.2 |
kasA | 2519236 | p.Glu374Asp | missense_variant | 0.33 |
eis | 2714458 | p.Asp292Val | missense_variant | 0.15 |
eis | 2714541 | c.792A>G | synonymous_variant | 0.11 |
eis | 2714989 | p.Val115Asp | missense_variant | 0.17 |
folC | 2747599 | c.-1A>T | upstream_gene_variant | 0.15 |
ribD | 2987188 | p.Leu117Pro | missense_variant | 0.11 |
ribD | 2987315 | c.477C>T | synonymous_variant | 0.17 |
thyA | 3074431 | p.Thr14Lys | missense_variant | 0.13 |
thyA | 3074454 | c.18C>T | synonymous_variant | 0.15 |
ald | 3087271 | p.Arg151Leu | missense_variant | 0.18 |
ald | 3087280 | p.Gly154Glu | missense_variant | 0.2 |
Rv3236c | 3612103 | p.Leu338Phe | missense_variant | 0.12 |
fbiA | 3641378 | p.Arg279Gln | missense_variant | 0.14 |
fbiB | 3642027 | c.494delT | frameshift_variant | 0.12 |
fbiB | 3642031 | p.Gly166Ala | missense_variant | 0.12 |
fbiB | 3642033 | c.499_500insA | frameshift_variant | 0.12 |
fbiB | 3642037 | c.503_504insGGCAT | frameshift_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.24 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.14 |
rpoA | 3877853 | p.Phe219Leu | missense_variant | 0.4 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.18 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.18 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.2 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.37 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.23 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244214 | p.Ala328Thr | missense_variant | 0.12 |
embA | 4244654 | p.Gln474His | missense_variant | 0.18 |
embA | 4244759 | c.1527C>T | synonymous_variant | 0.17 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.18 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.45 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.8 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.8 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.56 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.64 |
embB | 4246881 | p.Val123Gly | missense_variant | 0.15 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.12 |
embB | 4249588 | c.3075C>A | synonymous_variant | 0.17 |
aftB | 4268022 | p.Leu272Pro | missense_variant | 0.2 |
aftB | 4268481 | p.Pro119Gln | missense_variant | 0.13 |
ubiA | 4269044 | p.Val264Leu | missense_variant | 0.12 |
ubiA | 4269426 | c.407delT | frameshift_variant | 0.18 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.2 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.19 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.19 |
ethA | 4327662 | c.-189C>T | upstream_gene_variant | 0.15 |
ethR | 4327924 | p.Ala126Ser | missense_variant | 0.14 |
ethR | 4327954 | p.Glu136Lys | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |