Run ID: SRR21677883
Sample name:
Date: 04-04-2023 02:49:41
Number of reads: 833680
Percentage reads mapped: 84.99
Strain: lineage4.1.1.2
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.14 | streptomycin |
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 |
ccsA | 619925 | p.Arg12His | missense_variant | 0.13 |
rpoB | 762943 | p.Ile1046Asn | missense_variant | 0.13 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775972 | p.Ala837Ser | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302814 | c.-117C>T | upstream_gene_variant | 1.0 |
fbiC | 1304422 | p.Ala498Ser | missense_variant | 0.17 |
fbiC | 1304437 | c.1508delA | frameshift_variant | 0.18 |
fbiC | 1304442 | c.1512T>C | synonymous_variant | 0.17 |
fbiC | 1304443 | p.Ala505Thr | missense_variant | 0.17 |
fbiC | 1304446 | c.1516_1517insT | frameshift_variant | 0.17 |
embR | 1417008 | c.339delG | frameshift_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473291 | n.1446G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.15 |
inhA | 1674504 | c.306dupG | frameshift_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyX | 3067534 | p.Ala138Thr | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087792 | p.Ala325Ser | missense_variant | 0.11 |
Rv3083 | 3449670 | c.1167C>T | synonymous_variant | 0.11 |
Rv3083 | 3449787 | c.1284C>T | synonymous_variant | 1.0 |
Rv3083 | 3449873 | c.1371delG | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475010 | p.Asp335Val | missense_variant | 0.12 |
rpoA | 3878535 | c.-28G>T | upstream_gene_variant | 0.15 |
rpoA | 3878619 | c.-113delC | upstream_gene_variant | 0.33 |
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 | 4243513 | p.Pro94Gln | missense_variant | 0.12 |
embA | 4243833 | p.Ala201Thr | missense_variant | 1.0 |
embA | 4244247 | p.Val339Ile | missense_variant | 0.15 |
embA | 4245555 | p.Glu775* | stop_gained | 0.11 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.11 |
embB | 4246930 | p.Gln139His | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4267792 | p.Pro349Ala | missense_variant | 0.11 |
aftB | 4267943 | p.Tyr298* | stop_gained | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |