Run ID: SRR4034800
Sample name:
Date: 04-04-2023 07:05:06
Number of reads: 138366
Percentage reads mapped: 99.6
Strain: lineage4.9;lineage4.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.81 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.11 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918074 | c.138_139delGT | frameshift_variant | 1.0 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6003 | c.765delT | frameshift_variant | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
fbiC | 1303825 | p.Glu299Lys | missense_variant | 0.33 |
fbiC | 1304045 | p.Pro372His | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918520 | p.Pro194Arg | missense_variant | 0.67 |
Rv1979c | 2221740 | c.1425C>T | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289464 | c.-223A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612693 | p.Arg142Trp | missense_variant | 0.67 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
clpC1 | 4038245 | c.2460C>T | synonymous_variant | 1.0 |
embC | 4240293 | p.Leu144Pro | missense_variant | 0.67 |
embC | 4240793 | p.Ala311Thr | missense_variant | 0.67 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embC | 4241355 | p.Gln498Arg | missense_variant | 0.25 |
embC | 4241655 | p.Gly598Glu | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242751 | c.-482G>A | upstream_gene_variant | 0.67 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245327 | p.Ala699Thr | missense_variant | 0.67 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |