Run ID: ERR4407542
Sample name:
Date: 01-04-2023 05:49:19
Number of reads: 336684
Percentage reads mapped: 99.65
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 | 7600 | p.Ala100Asp | missense_variant | 0.2 |
gyrA | 7811 | c.510C>T | synonymous_variant | 0.11 |
mshA | 576686 | c.1340delA | frameshift_variant | 0.33 |
rpoB | 761548 | p.Val581Gly | missense_variant | 0.13 |
rpoB | 762711 | p.Pro969Ser | missense_variant | 0.14 |
rpoB | 762869 | p.Tyr1021* | stop_gained | 0.11 |
rpoC | 764467 | c.1098C>A | synonymous_variant | 0.14 |
rpoC | 764752 | c.1383G>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777829 | p.Met218Leu | missense_variant | 0.18 |
mmpS5 | 778640 | p.Ser89Leu | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801080 | p.Ala91Val | missense_variant | 0.12 |
fbiC | 1303161 | c.231G>A | synonymous_variant | 0.2 |
fbiC | 1303210 | p.Val94Phe | missense_variant | 0.12 |
fbiC | 1303272 | c.342A>T | synonymous_variant | 0.15 |
fbiC | 1304904 | c.1974G>A | synonymous_variant | 0.18 |
Rv1258c | 1406795 | c.546G>A | synonymous_variant | 0.17 |
embR | 1417091 | p.Ala86Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473333 | n.1488T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475863 | n.2206G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476641 | n.2984T>C | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155067 | p.Gly349Cys | missense_variant | 0.12 |
katG | 2155167 | c.945C>T | synonymous_variant | 0.11 |
katG | 2155332 | c.780C>T | synonymous_variant | 0.33 |
katG | 2156044 | p.Val23Ala | missense_variant | 0.33 |
katG | 2156367 | c.-256G>A | upstream_gene_variant | 0.18 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169752 | c.861C>T | synonymous_variant | 0.5 |
PPE35 | 2170162 | p.Met151Leu | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518910 | c.796C>T | synonymous_variant | 0.17 |
eis | 2714415 | c.918G>A | synonymous_variant | 0.13 |
folC | 2746408 | c.1191G>A | synonymous_variant | 0.25 |
pepQ | 2859700 | p.Gly240Asp | missense_variant | 0.14 |
pepQ | 2859801 | c.618G>A | synonymous_variant | 0.17 |
Rv2752c | 3065572 | p.Glu207Gly | missense_variant | 0.17 |
thyA | 3074168 | c.303delG | frameshift_variant | 0.12 |
ald | 3086636 | c.-184A>G | upstream_gene_variant | 0.12 |
ald | 3086646 | c.-174G>T | upstream_gene_variant | 0.13 |
fprA | 3474063 | c.57G>C | synonymous_variant | 0.11 |
fprA | 3474138 | c.132T>C | synonymous_variant | 0.12 |
fprA | 3474780 | c.774C>A | synonymous_variant | 0.12 |
fprA | 3475367 | p.Gly454Val | missense_variant | 0.4 |
fbiA | 3641524 | p.Gly328Arg | missense_variant | 0.25 |
rpoA | 3878484 | c.22_23dupAC | frameshift_variant | 0.22 |
clpC1 | 4038744 | p.Thr654Met | missense_variant | 0.13 |
clpC1 | 4039123 | p.Val528Leu | missense_variant | 0.14 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
clpC1 | 4040364 | p.Arg114Gln | missense_variant | 0.1 |
embC | 4239936 | c.75dupC | frameshift_variant | 0.12 |
embA | 4242304 | c.-929G>C | upstream_gene_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243347 | p.Thr39Ala | missense_variant | 0.1 |
embA | 4244539 | p.Ala436Val | missense_variant | 0.13 |
embA | 4244872 | p.Gly547Val | missense_variant | 0.22 |
embA | 4245325 | p.Val698Ala | missense_variant | 0.17 |
embA | 4245561 | p.Val777Met | missense_variant | 0.12 |
aftB | 4267430 | c.1406delC | frameshift_variant | 0.14 |
aftB | 4267782 | p.Val352Gly | missense_variant | 1.0 |
ubiA | 4269482 | p.Trp118Arg | missense_variant | 0.14 |
aftB | 4269684 | c.-848G>A | upstream_gene_variant | 0.13 |
ethA | 4328216 | c.-743C>A | upstream_gene_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |