Run ID: ERR4819947
Sample name:
Date: 01-04-2023 16:23:45
Number of reads: 711782
Percentage reads mapped: 99.07
Strain: lineage4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | 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 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.95 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.29 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.15 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.15 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766070 | c.2701C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.19 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.19 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.18 |
mmpL5 | 778185 | p.Arg99Pro | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155031 | p.Ala361Thr | missense_variant | 0.14 |
katG | 2155594 | p.Leu173Gln | missense_variant | 0.11 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.19 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170189 | p.Glu142Gln | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.1 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.11 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474767 | p.Gly254Ala | missense_variant | 1.0 |
Rv3236c | 3613099 | c.18G>A | synonymous_variant | 0.12 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.13 |
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 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407822 | p.Gln127His | missense_variant | 0.11 |