Run ID: SRR4037884
Sample name:
Date: 04-04-2023 07:44:35
Number of reads: 1039107
Percentage reads mapped: 99.7
Strain: lineage4.3.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154893 | c.1218delC | frameshift_variant | 0.18 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9036 | p.Ala579Thr | missense_variant | 0.12 |
gyrA | 9300 | p.Ala667Pro | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491124 | c.342C>T | synonymous_variant | 0.12 |
rpoC | 764671 | c.1302G>A | synonymous_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778303 | p.Gln60Lys | missense_variant | 0.12 |
mmpR5 | 779123 | p.Val45Ala | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.12 |
fbiC | 1304965 | p.Val679Met | missense_variant | 0.12 |
embR | 1416677 | p.Ala224Glu | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169097 | c.1515delG | frameshift_variant | 0.33 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.4 |
Rv1979c | 2222893 | p.Gly91Val | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289496 | c.-255G>A | upstream_gene_variant | 0.17 |
kasA | 2519332 | c.1218C>A | synonymous_variant | 0.13 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339697 | p.Asp194Asn | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474360 | p.Asp118Glu | missense_variant | 0.12 |
Rv3236c | 3612523 | c.594G>A | synonymous_variant | 0.17 |
rpoA | 3877851 | c.657C>T | synonymous_variant | 0.13 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.2 |
clpC1 | 4039768 | p.Ala313Thr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247171 | c.658C>T | synonymous_variant | 0.22 |
embB | 4249613 | p.Gly1034Ser | missense_variant | 0.11 |
aftB | 4269096 | c.-260C>T | upstream_gene_variant | 0.11 |
ethA | 4327300 | p.Asp58Glu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |