Run ID: ERR2229642
Sample name:
Date: 31-03-2023 17:23:23
Number of reads: 1077486
Percentage reads mapped: 99.29
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 |
gyrA | 7852 | p.Gly184Val | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775988 | c.2493G>T | synonymous_variant | 0.13 |
mmpL5 | 778973 | c.-493T>C | upstream_gene_variant | 0.17 |
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 | 1475327 | n.1670G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475362 | n.1706dupC | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674324 | c.123C>T | synonymous_variant | 0.18 |
tlyA | 1917819 | c.-121C>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168235 | p.Ala793Glu | missense_variant | 0.15 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169101 | c.1512G>C | synonymous_variant | 0.12 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.18 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.15 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.21 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.37 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.38 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288992 | p.Ser84Arg | missense_variant | 0.1 |
pncA | 2290050 | c.-809G>T | upstream_gene_variant | 0.14 |
folC | 2746619 | p.Arg327Leu | missense_variant | 0.12 |
pepQ | 2860058 | c.361T>C | synonymous_variant | 0.11 |
Rv2752c | 3065945 | p.His83Tyr | missense_variant | 0.14 |
thyX | 3067307 | c.639C>T | synonymous_variant | 0.17 |
fprA | 3474245 | p.Gly80Asp | missense_variant | 0.15 |
Rv3236c | 3612679 | c.438G>T | synonymous_variant | 0.2 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.16 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.16 |
clpC1 | 4040274 | p.Gly144Val | missense_variant | 0.11 |
clpC1 | 4040316 | p.Glu130Gly | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4266976 | c.1860delG | frameshift_variant | 0.1 |
aftB | 4267858 | p.Ile327Leu | missense_variant | 0.17 |
aftB | 4268697 | p.Pro47Leu | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |