Run ID: ERR1950052
Sample name:
Date: 31-03-2023 15:38:35
Number of reads: 708782
Percentage reads mapped: 99.63
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 |
---|---|---|---|---|
gyrB | 6591 | p.Arg451His | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575207 | c.-141A>G | upstream_gene_variant | 0.13 |
mshA | 576535 | c.1188T>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775795 | p.Ala896Ser | missense_variant | 0.13 |
mmpL5 | 777370 | p.Lys371* | stop_gained | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303273 | p.Arg115Cys | missense_variant | 0.15 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407130 | p.Arg71Cys | missense_variant | 0.15 |
Rv1258c | 1407423 | c.-83G>C | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475962 | n.2305G>A | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673620 | p.Asp61His | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156519 | c.-408T>C | upstream_gene_variant | 0.14 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.22 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.22 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168989 | p.Thr542Ser | missense_variant | 0.23 |
PPE35 | 2169049 | p.Ile522Phe | missense_variant | 0.22 |
PPE35 | 2169144 | p.Val490Glu | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
fprA | 3474084 | c.78C>T | synonymous_variant | 0.12 |
fprA | 3474140 | p.Pro45His | missense_variant | 0.11 |
whiB7 | 3568523 | c.157T>C | synonymous_variant | 0.13 |
Rv3236c | 3612456 | c.661C>A | synonymous_variant | 0.12 |
fbiA | 3640509 | c.-34T>C | upstream_gene_variant | 0.11 |
clpC1 | 4040106 | p.Val200Gly | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243864 | p.Val211Gly | missense_variant | 0.18 |
embA | 4244613 | p.Ala461Thr | missense_variant | 0.22 |
aftB | 4267895 | p.Phe314Leu | missense_variant | 0.17 |
aftB | 4268557 | p.Gly94Arg | missense_variant | 0.1 |
ethA | 4328473 | c.-1000G>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |