Run ID: ERR2229773
Sample name:
Date: 31-03-2023 17:35:01
Number of reads: 379980
Percentage reads mapped: 99.64
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 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.35 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407084 | p.Val86Gly | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473117 | n.1272A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475075 | n.1418A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476410 | n.2753C>A | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673863 | p.Ser142Pro | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918066 | p.Ala43Pro | missense_variant | 0.5 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.33 |
ndh | 2102932 | p.Asp37Glu | missense_variant | 0.12 |
katG | 2155540 | p.Trp191Leu | missense_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
Rv1979c | 2222186 | p.Trp327Gly | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289973 | c.-732T>C | upstream_gene_variant | 0.22 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.22 |
Rv2752c | 3064631 | p.Ala521Thr | missense_variant | 0.13 |
thyA | 3074393 | p.Arg27Ser | missense_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
embC | 4240249 | p.Asp129Glu | missense_variant | 0.14 |
embC | 4240275 | p.Pro138Gln | missense_variant | 0.12 |
embC | 4241473 | c.1611G>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268557 | p.Gly94* | stop_gained | 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 |