Run ID: ERR2229052
Sample name:
Date: 31-03-2023 16:32:46
Number of reads: 972238
Percentage reads mapped: 99.44
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 | 7287 | c.-15G>C | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.21 |
mshA | 576123 | p.Leu259Arg | missense_variant | 0.18 |
mshA | 576290 | p.Leu315Phe | missense_variant | 0.15 |
ccsA | 620486 | p.Arg199Leu | missense_variant | 0.17 |
ccsA | 620578 | p.Tyr230His | missense_variant | 0.11 |
rpoC | 766367 | p.Ala1000Ser | missense_variant | 0.14 |
rpoC | 766799 | p.Ala1144Thr | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776368 | p.Leu705Met | missense_variant | 0.13 |
mmpL5 | 777590 | c.891G>A | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303795 | p.Glu289* | stop_gained | 0.12 |
fbiC | 1304156 | p.Arg409Leu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472393 | n.548G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474126 | n.469G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476055 | n.2398C>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.13 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.19 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.11 |
eis | 2715510 | c.-178G>T | upstream_gene_variant | 0.15 |
pepQ | 2859646 | p.Gln258Arg | missense_variant | 0.25 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.15 |
fprA | 3475035 | c.1029C>T | synonymous_variant | 0.12 |
fprA | 3475167 | c.1161C>A | synonymous_variant | 0.12 |
fbiB | 3641803 | p.Asp90Val | missense_variant | 0.12 |
fbiB | 3642103 | p.Thr190Asn | missense_variant | 0.11 |
rpoA | 3877963 | p.Arg182Pro | missense_variant | 0.14 |
embC | 4241807 | p.Pro649Ser | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243785 | p.Leu185Met | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.25 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.25 |
embB | 4249653 | c.3141delC | frameshift_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |