Run ID: SRR22196586
Sample name:
Date: 04-04-2023 04:06:14
Number of reads: 415497
Percentage reads mapped: 18.41
Strain: lineage4.1.2.1
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 |
lineage4.1.2 | 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 |
---|---|---|---|---|---|
pncA | 2288971 | p.Glu91* | stop_gained | 0.2 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7263 | p.Val675Ala | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9345 | p.Arg682Gly | missense_variant | 0.29 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760060 | p.Tyr85Cys | missense_variant | 0.17 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 763101 | p.Ala1099Thr | missense_variant | 0.29 |
rpoB | 763111 | p.Lys1102Arg | missense_variant | 0.25 |
rpoC | 764059 | c.693delC | frameshift_variant | 0.2 |
rpoC | 765110 | p.Met581Val | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765506 | p.Val713Ile | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775723 | p.Ile920Val | missense_variant | 0.2 |
mmpL5 | 776926 | p.Thr519Ala | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303364 | p.Phe145Ser | missense_variant | 0.12 |
fbiC | 1303438 | p.Thr170Ser | missense_variant | 0.29 |
fbiC | 1304632 | p.Ala568Ser | missense_variant | 0.15 |
fbiC | 1305176 | p.Ser749* | stop_gained | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475174 | n.1517C>T | non_coding_transcript_exon_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101921 | c.1122G>T | synonymous_variant | 0.2 |
ndh | 2103113 | c.-71C>G | upstream_gene_variant | 0.15 |
ndh | 2103134 | c.-92T>A | upstream_gene_variant | 0.13 |
PPE35 | 2170571 | p.Leu14Phe | missense_variant | 0.17 |
Rv1979c | 2222243 | p.Ala308Pro | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746473 | p.Val376Ile | missense_variant | 0.4 |
thyX | 3067874 | c.72C>A | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3613142 | c.-26A>G | upstream_gene_variant | 0.25 |
embC | 4240246 | c.384C>T | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246280 | c.-234G>T | upstream_gene_variant | 1.0 |
embB | 4248015 | p.Thr501Arg | missense_variant | 0.15 |
aftB | 4268279 | c.558G>A | synonymous_variant | 0.29 |
aftB | 4269252 | c.-416C>T | upstream_gene_variant | 0.17 |
ethR | 4327760 | p.Val71Glu | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408129 | p.Ala25Val | missense_variant | 0.13 |