Run ID: ERR4132444
Sample name:
Date: 01-04-2023 04:30:16
Number of reads: 658822
Percentage reads mapped: 99.44
Strain: lineage4.2.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.99 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | 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 | 1.0 |
mshA | 575221 | c.-127C>T | upstream_gene_variant | 0.14 |
mshA | 575669 | c.322C>T | synonymous_variant | 0.15 |
rpoB | 763038 | c.3234_3235delCC | frameshift_variant | 0.12 |
rpoC | 765179 | p.Gly604Arg | missense_variant | 0.12 |
rpoC | 766350 | p.Ala994Asp | missense_variant | 0.12 |
rpoC | 766860 | p.Arg1164Leu | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777224 | c.1257C>T | synonymous_variant | 0.12 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
mmpL5 | 777880 | p.Asp201Tyr | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303875 | c.945G>A | synonymous_variant | 0.14 |
Rv1258c | 1407185 | p.Met52Ile | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833438 | c.-104C>T | upstream_gene_variant | 0.13 |
rpsA | 1834353 | p.Arg271Leu | missense_variant | 0.14 |
rpsA | 1834658 | p.Phe373Leu | missense_variant | 0.17 |
tlyA | 1917957 | c.18C>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918059 | c.120C>A | synonymous_variant | 0.25 |
ndh | 2102362 | p.Lys227Asn | missense_variant | 0.13 |
ndh | 2102449 | p.Lys198Asn | missense_variant | 0.13 |
ndh | 2103023 | p.Pro7Leu | missense_variant | 1.0 |
katG | 2154598 | p.Trp505Leu | missense_variant | 0.12 |
katG | 2155758 | c.354C>A | synonymous_variant | 0.13 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.96 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.37 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.39 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518058 | c.-57G>T | upstream_gene_variant | 0.18 |
eis | 2714937 | c.396G>T | synonymous_variant | 0.29 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
ribD | 2987520 | p.Val228Met | missense_variant | 0.12 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448571 | p.Val23Ala | missense_variant | 0.15 |
Rv3083 | 3448899 | c.396C>A | synonymous_variant | 0.12 |
Rv3083 | 3449207 | p.Pro235Gln | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475267 | p.Ala421Thr | missense_variant | 0.17 |
Rv3236c | 3612183 | p.Ala312Ser | missense_variant | 0.22 |
fbiB | 3642063 | p.Ala177Ser | missense_variant | 0.17 |
clpC1 | 4038428 | c.2277G>A | synonymous_variant | 0.17 |
clpC1 | 4039467 | p.Arg413Leu | missense_variant | 0.29 |
embC | 4240655 | p.Ala265Pro | missense_variant | 0.3 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244612 | c.1380C>A | synonymous_variant | 0.13 |
embA | 4245703 | p.Ser824Leu | missense_variant | 0.13 |
ubiA | 4269198 | p.Ser212Arg | missense_variant | 0.12 |
ubiA | 4269272 | p.Val188Leu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |