Run ID: ERR1679648
Sample name:
Date: 31-03-2023 14:55:31
Number of reads: 515953
Percentage reads mapped: 99.63
Strain: lineage4.6.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575373 | p.Gly9Ala | missense_variant | 0.12 |
rpoC | 767223 | c.3857delC | frameshift_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
mmpR5 | 779311 | p.Ile108Val | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673945 | p.Arg169His | missense_variant | 0.11 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918264 | p.Val109Leu | missense_variant | 0.13 |
tlyA | 1918510 | p.Gln191* | stop_gained | 0.12 |
ndh | 2101839 | p.Ala402Thr | missense_variant | 0.22 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.89 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289247 | c.-6G>A | upstream_gene_variant | 0.1 |
pncA | 2290207 | c.-966G>A | upstream_gene_variant | 0.17 |
kasA | 2518449 | p.Val112Asp | missense_variant | 0.12 |
kasA | 2518454 | p.Thr114Ala | missense_variant | 0.12 |
kasA | 2518733 | p.Ile207Val | missense_variant | 0.2 |
eis | 2715093 | c.240C>T | synonymous_variant | 0.29 |
folC | 2746977 | p.Asp208Asn | missense_variant | 1.0 |
Rv2752c | 3065058 | c.1134C>T | synonymous_variant | 0.1 |
Rv2752c | 3065382 | p.Met270Ile | missense_variant | 0.14 |
Rv2752c | 3065790 | c.402C>T | synonymous_variant | 0.11 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
ald | 3086745 | c.-75G>C | upstream_gene_variant | 1.0 |
ald | 3086809 | c.-11_-10insA | upstream_gene_variant | 0.18 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
Rv3083 | 3448954 | p.Pro151Ser | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640772 | p.Arg77His | missense_variant | 0.17 |
fbiB | 3641908 | p.Pro125Arg | missense_variant | 0.11 |
rpoA | 3877484 | p.Ala342Thr | missense_variant | 0.11 |
embC | 4241556 | p.Ser565Ile | missense_variant | 0.22 |
embC | 4241579 | p.Ile573Phe | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243121 | p.Ser1087Gly | missense_variant | 0.1 |
embA | 4243687 | p.Phe152Tyr | missense_variant | 0.14 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
aftB | 4268227 | p.Ala204Thr | missense_variant | 0.1 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338610 | c.-89G>T | upstream_gene_variant | 1.0 |