Run ID: ERR403413
Sample name:
Date: 01-04-2023 04:28:22
Number of reads: 305964
Percentage reads mapped: 99.42
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5662 | c.423C>T | synonymous_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7643 | c.342C>T | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.23 |
mshA | 575585 | p.Ala80Thr | missense_variant | 0.33 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576281 | p.Leu312Met | missense_variant | 0.25 |
mshA | 576293 | p.Ala316Pro | missense_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762006 | p.Arg734Ser | missense_variant | 0.22 |
rpoC | 764330 | p.Pro321Ser | missense_variant | 0.29 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778694 | p.Tyr71Ser | missense_variant | 0.25 |
mmpS5 | 779591 | c.-686C>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.5 |
Rv1258c | 1406254 | p.Gly363Ser | missense_variant | 0.33 |
Rv1258c | 1406274 | p.Ala356Val | missense_variant | 0.4 |
Rv1258c | 1406322 | p.Ala340Val | missense_variant | 0.4 |
Rv1258c | 1406400 | p.Ile314Thr | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834273 | p.His244Gln | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102827 | c.216C>T | synonymous_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.38 |
katG | 2155856 | p.Thr86Pro | missense_variant | 0.43 |
katG | 2156453 | c.-342C>T | upstream_gene_variant | 0.25 |
PPE35 | 2168499 | p.Ser705Leu | missense_variant | 0.18 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.5 |
PPE35 | 2169862 | p.Asn251His | missense_variant | 0.6 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518967 | p.Val285Ile | missense_variant | 0.33 |
kasA | 2519326 | c.1212C>T | synonymous_variant | 0.33 |
ahpC | 2725959 | c.-234C>G | upstream_gene_variant | 0.22 |
folC | 2747770 | c.-172T>C | upstream_gene_variant | 0.22 |
pepQ | 2859536 | p.Gly295* | stop_gained | 0.25 |
Rv2752c | 3064585 | p.Thr536Met | missense_variant | 0.13 |
Rv2752c | 3064676 | p.Pro506Ser | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087604 | p.Ala262Glu | missense_variant | 0.18 |
Rv3083 | 3448995 | c.492G>A | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474525 | p.Leu173Phe | missense_variant | 0.5 |
fbiA | 3641245 | p.Glu235Gln | missense_variant | 0.4 |
fbiB | 3641784 | p.Arg84Cys | missense_variant | 0.4 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 0.2 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.5 |
clpC1 | 4038562 | p.Asp715Asn | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243111 | c.-122C>T | upstream_gene_variant | 0.25 |
embA | 4244897 | c.1665T>A | synonymous_variant | 0.25 |
embB | 4246840 | c.327C>A | synonymous_variant | 0.25 |
aftB | 4267089 | p.Thr583Asn | missense_variant | 0.93 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |