Run ID: SRR6896163
Sample name:
Date: 04-04-2023 17:57:25
Number of reads: 374111
Percentage reads mapped: 99.17
Strain: lineage4.4.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 0.98 |
lineage4.4.2 | Euro-American | T1;T2 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7239 | p.Ala667Asp | missense_variant | 0.15 |
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 | 576031 | c.686delG | frameshift_variant | 0.12 |
ccsA | 620096 | p.His69Pro | missense_variant | 0.67 |
rpoB | 760539 | p.Arg245Trp | missense_variant | 0.11 |
rpoC | 766150 | c.2781C>A | synonymous_variant | 0.12 |
rpoC | 766691 | p.Gly1108Cys | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775857 | p.Gly875Ala | missense_variant | 0.15 |
mmpL5 | 776153 | p.Leu776Phe | missense_variant | 0.12 |
mmpL5 | 777642 | p.Phe280Ser | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304264 | p.Gly445Val | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472220 | n.375G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102708 | p.Tyr112Cys | missense_variant | 0.15 |
PPE35 | 2168757 | p.Gln619Arg | missense_variant | 1.0 |
PPE35 | 2168780 | p.His611Gln | missense_variant | 0.18 |
PPE35 | 2168961 | p.Gly551Val | missense_variant | 0.13 |
PPE35 | 2170096 | p.Arg173Trp | missense_variant | 0.14 |
PPE35 | 2170694 | c.-82T>C | upstream_gene_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.2 |
eis | 2714615 | p.Glu240Gln | missense_variant | 0.12 |
Rv2752c | 3065625 | c.567G>A | synonymous_variant | 0.15 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
Rv2752c | 3066322 | c.-131G>T | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448348 | c.-156G>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642776 | c.1242G>A | synonymous_variant | 0.33 |
alr | 3840212 | c.1209C>T | synonymous_variant | 1.0 |
clpC1 | 4038162 | p.Arg848Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246031 | c.-483G>A | upstream_gene_variant | 0.29 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
embB | 4247249 | p.Gly246Arg | missense_variant | 1.0 |
embB | 4248246 | p.Ile578Ser | missense_variant | 0.12 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
ubiA | 4269712 | p.Gly41Val | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |