Run ID: ERR4407449
Sample name:
Date: 01-04-2023 05:44:34
Number of reads: 433752
Percentage reads mapped: 99.57
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 | 620253 | c.363G>A | synonymous_variant | 0.11 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.21 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474715 | n.1061delA | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673668 | p.Glu77Lys | missense_variant | 0.17 |
rpsA | 1833481 | c.-61T>C | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102430 | c.611_612delTC | frameshift_variant | 0.12 |
ndh | 2102482 | c.561A>T | synonymous_variant | 0.13 |
ndh | 2102538 | p.Lys169Gln | missense_variant | 0.12 |
katG | 2156348 | c.-237A>G | upstream_gene_variant | 0.12 |
PPE35 | 2168031 | p.Thr861Lys | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.27 |
Rv1979c | 2222868 | c.297C>G | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289412 | c.-171C>T | upstream_gene_variant | 0.14 |
ribD | 2986963 | p.Arg42Leu | missense_variant | 0.12 |
Rv2752c | 3065726 | p.Ile156Leu | missense_variant | 0.11 |
fprA | 3474098 | p.Asp31Gly | missense_variant | 0.17 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.29 |
alr | 3841272 | p.Arg50Gln | missense_variant | 0.12 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 0.11 |
embC | 4240409 | p.Pro183Ser | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.17 |
embA | 4245532 | p.Ile767Asn | missense_variant | 0.12 |
embA | 4246185 | p.Ala985Ser | missense_variant | 0.12 |
ubiA | 4269368 | p.Ala156Thr | missense_variant | 0.18 |
ubiA | 4269817 | p.Val6Glu | 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 |