Run ID: ERR4816524
Sample name:
Date: 01-04-2023 14:28:34
Number of reads: 134842
Percentage reads mapped: 88.26
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 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 |
rpoB | 759810 | p.Ala2Thr | missense_variant | 0.5 |
rpoB | 762300 | p.Lys832* | stop_gained | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
pncA | 2289547 | c.-307delC | upstream_gene_variant | 1.0 |
kasA | 2518387 | c.273C>A | synonymous_variant | 0.67 |
kasA | 2518896 | p.Pro261Leu | missense_variant | 0.33 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
ribD | 2987205 | c.369delC | frameshift_variant | 0.5 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.33 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.29 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.25 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.29 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
fbiB | 3641565 | p.Thr11Ser | missense_variant | 0.5 |
alr | 3840555 | p.Ala289Val | missense_variant | 0.33 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243623 | p.Ile131Val | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ubiA | 4269637 | c.196delG | frameshift_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407681 | p.His174Gln | missense_variant | 1.0 |