Run ID: ERR1950080
Sample name:
Date: 31-03-2023 15:39:19
Number of reads: 502223
Percentage reads mapped: 99.31
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 | 5488 | c.249C>A | synonymous_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.11 |
mshA | 576752 | p.Pro469Ser | missense_variant | 0.22 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.11 |
rpoB | 763285 | p.Leu1160Pro | missense_variant | 0.14 |
rpoB | 763325 | c.3519A>C | stop_lost&splice_region_variant | 0.17 |
rpoC | 763924 | c.555G>A | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776011 | p.Gln824* | stop_gained | 0.18 |
mmpL5 | 776788 | p.Glu565* | stop_gained | 0.17 |
mmpR5 | 778355 | c.-635G>T | upstream_gene_variant | 0.12 |
mmpL5 | 779022 | c.-542G>C | upstream_gene_variant | 0.11 |
mmpR5 | 779055 | p.Gln22His | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303613 | p.Leu228Pro | missense_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304513 | p.Val528Asp | missense_variant | 0.11 |
fbiC | 1305009 | c.2079C>A | synonymous_variant | 0.15 |
Rv1258c | 1406749 | p.Lys198Glu | missense_variant | 0.11 |
Rv1258c | 1407322 | p.Gly7Arg | missense_variant | 0.1 |
atpE | 1460964 | c.-81C>G | upstream_gene_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473963 | n.306G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474289 | n.632C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474300 | n.643C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475955 | n.2298A>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673368 | c.-72A>T | upstream_gene_variant | 0.11 |
inhA | 1674226 | c.28_34delATTCTGG | frameshift_variant | 0.2 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918370 | p.Ile144Asn | missense_variant | 0.13 |
ndh | 2103089 | c.-47C>A | upstream_gene_variant | 0.14 |
katG | 2155089 | p.Trp341* | stop_gained | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169022 | p.Gly531Trp | missense_variant | 0.4 |
PPE35 | 2169063 | p.Met517Lys | missense_variant | 0.33 |
PPE35 | 2169593 | c.1020C>A | synonymous_variant | 0.18 |
Rv1979c | 2222431 | p.Met245Thr | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289027 | p.Cys72Phe | missense_variant | 0.13 |
kasA | 2519243 | p.Asp377Asn | missense_variant | 0.12 |
eis | 2715288 | c.45G>T | synonymous_variant | 0.22 |
ahpC | 2726269 | p.Val26Asp | missense_variant | 0.24 |
fprA | 3474702 | c.696C>T | synonymous_variant | 0.12 |
fbiB | 3641361 | c.-174C>T | upstream_gene_variant | 0.18 |
alr | 3841207 | p.His72Tyr | missense_variant | 0.11 |
clpC1 | 4038705 | p.Asn667Ser | missense_variant | 0.12 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.2 |
embC | 4241427 | p.Leu522Gln | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243160 | c.-73C>G | upstream_gene_variant | 0.12 |
embA | 4243584 | p.Phe118Leu | missense_variant | 0.18 |
embB | 4248486 | p.Ser658Ile | missense_variant | 0.11 |
embB | 4248505 | c.1995delG | frameshift_variant | 0.12 |
embB | 4248531 | p.Phe673Ser | missense_variant | 0.11 |
embB | 4248563 | p.Ala684Thr | missense_variant | 0.11 |
embB | 4249169 | p.Asn886Asp | missense_variant | 0.13 |
aftB | 4268286 | p.Leu184Pro | missense_variant | 0.11 |
aftB | 4268477 | c.360C>G | synonymous_variant | 0.5 |
ubiA | 4269137 | p.Tyr233Asp | missense_variant | 0.5 |
ubiA | 4269652 | p.Val61Ala | missense_variant | 0.14 |
ubiA | 4269701 | p.Arg45Ser | missense_variant | 0.2 |
ubiA | 4269715 | p.Leu40Trp | missense_variant | 0.2 |
ubiA | 4269919 | c.-86T>C | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407722 | p.Ala161Thr | missense_variant | 0.25 |
gid | 4407839 | p.Ser122Pro | missense_variant | 0.13 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |