Run ID: ERR2514495
Sample name:
Date: 31-03-2023 20:22:23
Number of reads: 915976
Percentage reads mapped: 99.66
Strain: lineage4.3.4.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.1 | Euro-American (LAM) | LAM1;LAM2 | RD174 | 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 |
fgd1 | 491576 | p.Pro265Gln | missense_variant | 0.13 |
rpoB | 763191 | p.Val1129Ile | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766260 | c.2893delG | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775802 | p.Met893Ile | missense_variant | 0.11 |
mmpL5 | 778099 | p.Asp128Tyr | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2222854 | p.Ile104Thr | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518141 | c.29dupG | frameshift_variant | 0.43 |
kasA | 2518177 | c.63G>T | synonymous_variant | 0.17 |
eis | 2715076 | p.Ala86Glu | missense_variant | 0.11 |
ribD | 2986674 | c.-165G>T | upstream_gene_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339145 | p.Ile10Phe | missense_variant | 0.12 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.22 |
fbiD | 3339757 | p.Arg214Gly | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039361 | c.1344C>A | synonymous_variant | 0.11 |
clpC1 | 4039991 | c.714G>A | synonymous_variant | 1.0 |
panD | 4044302 | c.-21C>A | upstream_gene_variant | 0.13 |
embC | 4242596 | p.Gly912Cys | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244292 | p.Leu354Met | missense_variant | 0.2 |
aftB | 4267585 | p.Thr418Ala | missense_variant | 0.1 |
aftB | 4268684 | c.153G>A | synonymous_variant | 0.1 |
ubiA | 4270011 | c.-178A>G | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |