Run ID: ERR4811990
Sample name:
Date: 01-04-2023 11:47:37
Number of reads: 759682
Percentage reads mapped: 99.4
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 | 8223 | p.Asp308His | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.38 |
ccsA | 619837 | c.-54G>T | upstream_gene_variant | 0.13 |
ccsA | 620114 | p.Arg75Pro | missense_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760555 | p.Glu250Gly | missense_variant | 1.0 |
rpoB | 761724 | c.1921delA | frameshift_variant | 0.17 |
rpoC | 762476 | c.-894C>A | upstream_gene_variant | 0.13 |
rpoC | 762521 | c.-849C>A | upstream_gene_variant | 0.13 |
rpoC | 763172 | c.-198G>T | upstream_gene_variant | 0.13 |
rpoC | 764457 | p.Pro363Gln | missense_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765490 | c.2121C>A | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776582 | p.Gln633His | missense_variant | 0.12 |
mmpL5 | 776867 | c.1614G>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781809 | p.Gly84Arg | missense_variant | 0.12 |
rplC | 801166 | p.Gly120Cys | missense_variant | 0.15 |
fbiC | 1302920 | c.-11G>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473694 | n.37C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473868 | n.211C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834129 | c.588C>A | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154437 | p.Ala559Thr | missense_variant | 0.11 |
katG | 2154551 | p.Leu521Met | missense_variant | 0.18 |
katG | 2156532 | c.-421C>T | upstream_gene_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289873 | c.-632C>A | upstream_gene_variant | 0.13 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746277 | p.Asp441Gly | missense_variant | 1.0 |
folC | 2746849 | c.750G>C | synonymous_variant | 0.11 |
pepQ | 2860406 | p.Gln5Lys | missense_variant | 0.17 |
Rv2752c | 3065999 | p.Arg65Cys | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087862 | p.Gly348Val | missense_variant | 0.15 |
fbiD | 3339402 | c.285C>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474104 | p.Asp33Gly | missense_variant | 0.13 |
fbiA | 3640849 | p.Glu103* | stop_gained | 0.12 |
fbiB | 3641358 | c.-177G>T | upstream_gene_variant | 0.14 |
alr | 3840661 | p.Gly254Cys | missense_variant | 0.12 |
rpoA | 3878163 | c.345C>A | synonymous_variant | 0.14 |
rpoA | 3878413 | p.Tyr32Cys | missense_variant | 0.13 |
clpC1 | 4039737 | p.Thr323Asn | missense_variant | 0.11 |
embC | 4241537 | p.Gly559Arg | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243896 | p.Ala222Ser | missense_variant | 0.11 |
embB | 4246928 | p.Gln139Lys | missense_variant | 0.11 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.23 |
embB | 4247055 | p.Leu181Gln | missense_variant | 0.2 |
embB | 4249766 | p.Arg1085Ser | missense_variant | 0.12 |
aftB | 4269282 | c.-446G>T | upstream_gene_variant | 0.12 |
ubiA | 4269380 | p.Val152Ile | missense_variant | 0.13 |
ethA | 4328308 | c.-835G>T | upstream_gene_variant | 0.12 |
ethA | 4328416 | c.-943G>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408283 | c.-81A>G | upstream_gene_variant | 1.0 |
gid | 4408388 | c.-186C>T | upstream_gene_variant | 0.12 |