Run ID: ERR5908131
Sample name:
Date: 02-04-2023 00:50:37
Number of reads: 1156035
Percentage reads mapped: 99.61
Strain: lineage4.1.1.2
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 | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.2 | Euro-American (X-type) | X1 | 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 | 8258 | c.957G>A | synonymous_variant | 0.2 |
gyrA | 8360 | c.1059G>A | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.28 |
rpoB | 759659 | c.-148T>G | upstream_gene_variant | 0.17 |
rpoB | 761402 | c.1596C>A | synonymous_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302814 | c.-117C>T | upstream_gene_variant | 1.0 |
embR | 1416225 | p.Glu375Lys | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471921 | n.76G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472125 | n.280G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472580 | n.735C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472846 | n.1001C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472849 | n.1004C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472941 | n.1096A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473211 | n.1366G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474199 | n.542G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474829 | n.1172C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475213 | n.1556C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475487 | n.1830C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475623 | n.1966C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476427 | n.2770G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476604 | n.2947G>A | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673482 | p.Ser15Pro | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167698 | p.Asn972Thr | missense_variant | 0.1 |
PPE35 | 2168301 | p.Thr771Asn | missense_variant | 0.12 |
PPE35 | 2168795 | c.1818G>A | synonymous_variant | 0.14 |
PPE35 | 2169366 | p.Ser416Asn | missense_variant | 0.15 |
Rv1979c | 2222841 | c.324G>T | synonymous_variant | 0.12 |
Rv1979c | 2223000 | c.165C>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448456 | c.-48G>T | upstream_gene_variant | 0.12 |
Rv3083 | 3449787 | c.1284C>T | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841477 | c.-57G>T | upstream_gene_variant | 0.16 |
rpoA | 3878455 | p.Arg18Leu | missense_variant | 0.17 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.15 |
embC | 4241572 | c.1710C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243833 | p.Ala201Thr | missense_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.32 |
embB | 4246930 | p.Gln139His | missense_variant | 1.0 |
embB | 4248301 | c.1791delG | frameshift_variant | 0.11 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ethR | 4327243 | c.-306G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |