Run ID: ERR2512872
Sample name:
Date: 31-03-2023 19:18:29
Number of reads: 750985
Percentage reads mapped: 98.67
Strain: lineage4.2.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | None | 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 | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575401 | c.54G>T | synonymous_variant | 0.12 |
rpoB | 760806 | p.Ala334Thr | missense_variant | 0.11 |
rpoB | 762461 | c.2657delA | frameshift_variant | 0.15 |
rpoC | 764626 | c.1257C>A | synonymous_variant | 0.1 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.1 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.11 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.11 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.11 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.11 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.11 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776168 | c.2313C>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475627 | n.1970G>T | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1674036 | c.598delC | frameshift_variant | 0.12 |
fabG1 | 1674152 | p.Pro238Gln | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102152 | c.891C>T | synonymous_variant | 0.12 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.17 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.27 |
ahpC | 2726426 | c.234C>T | synonymous_variant | 0.11 |
thyX | 3067540 | p.Ala136Thr | missense_variant | 0.12 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.93 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087008 | c.189G>A | synonymous_variant | 0.14 |
fbiD | 3339186 | c.69A>G | synonymous_variant | 0.1 |
fbiD | 3339751 | p.Ala212Thr | missense_variant | 0.11 |
Rv3083 | 3449982 | c.1479G>C | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3613127 | c.-12delA | upstream_gene_variant | 0.18 |
alr | 3840638 | c.783C>T | synonymous_variant | 0.12 |
rpoA | 3878648 | c.-141C>A | upstream_gene_variant | 0.5 |
clpC1 | 4039161 | p.His515Gly | missense_variant | 0.11 |
clpC1 | 4040043 | p.Gly221Asp | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246078 | p.Ser949Asn | missense_variant | 0.12 |
embB | 4246109 | c.-405C>A | upstream_gene_variant | 0.17 |
embB | 4249271 | p.Asp920Asn | missense_variant | 0.11 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.18 |
embB | 4249658 | p.Met1049Leu | missense_variant | 0.22 |
embB | 4249747 | c.3234C>T | synonymous_variant | 0.17 |
ubiA | 4269373 | p.Ser154Trp | missense_variant | 0.14 |
ethR | 4327569 | p.Ser7Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |