Run ID: ERR2228793
Sample name:
Date: 31-03-2023 16:21:13
Number of reads: 1174563
Percentage reads mapped: 99.4
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 | 7276 | c.-26T>A | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 759743 | c.-64G>A | upstream_gene_variant | 0.15 |
rpoC | 766910 | p.Ile1181Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777340 | p.Lys381* | stop_gained | 0.26 |
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 |
rrs | 1472538 | n.693A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474033 | n.376A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474062 | n.405A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475573 | n.1916G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476708 | n.3051C>A | non_coding_transcript_exon_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101718 | p.Leu442Arg | missense_variant | 0.25 |
katG | 2153912 | p.Leu734Ile | missense_variant | 0.15 |
PPE35 | 2168227 | p.Thr796Ser | missense_variant | 0.22 |
PPE35 | 2168607 | p.Met669Lys | missense_variant | 0.5 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169063 | p.Met517Lys | missense_variant | 0.25 |
PPE35 | 2169108 | p.Asp502Val | missense_variant | 0.22 |
Rv1979c | 2222522 | p.Lys215* | stop_gained | 0.18 |
Rv1979c | 2222573 | p.Ser198Ala | missense_variant | 0.18 |
Rv1979c | 2223066 | c.99C>T | synonymous_variant | 0.13 |
Rv1979c | 2223128 | p.Lys13Glu | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2987038 | p.Asp67Ala | missense_variant | 0.18 |
Rv2752c | 3065011 | p.Met394Thr | missense_variant | 0.12 |
fbiA | 3641015 | p.Asp158Ala | missense_variant | 0.27 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.25 |
clpC1 | 4039701 | p.Asp335Ala | missense_variant | 0.17 |
clpC1 | 4040524 | p.Ser61Cys | missense_variant | 0.18 |
embC | 4242393 | p.Asp844Ala | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268826 | p.Val4Gly | missense_variant | 0.33 |
ethA | 4327454 | p.Val7Ala | missense_variant | 0.11 |
ethR | 4327741 | p.Phe65Ile | 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 |