Run ID: ERR2515281
Sample name:
Date: 31-03-2023 20:51:02
Number of reads: 390507
Percentage reads mapped: 99.85
Strain: lineage4.3.3
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 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8508 | p.Glu403Lys | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575909 | p.Leu188Val | missense_variant | 1.0 |
mshA | 576619 | c.1272C>T | synonymous_variant | 0.12 |
ccsA | 620658 | c.768C>T | synonymous_variant | 0.1 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.12 |
rpoB | 763234 | p.Glu1143Val | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766159 | c.2790C>T | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778346 | c.-644G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474988 | n.1331C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475107 | n.1450G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475371 | n.1714T>A | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918540 | p.Pro201Thr | missense_variant | 0.18 |
tlyA | 1918601 | p.His221Arg | missense_variant | 0.22 |
PPE35 | 2168294 | p.Glu773Asp | missense_variant | 0.15 |
PPE35 | 2169254 | c.1359C>T | synonymous_variant | 0.11 |
Rv1979c | 2222749 | p.Leu139Pro | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289184 | p.Ala20Ser | missense_variant | 0.13 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2746664 | p.Phe312Tyr | missense_variant | 0.11 |
folC | 2747225 | p.Arg125Gln | missense_variant | 1.0 |
ribD | 2987313 | p.Leu159Phe | missense_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449308 | p.Leu269Met | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475074 | c.1068C>T | synonymous_variant | 0.14 |
whiB7 | 3568557 | c.123A>T | synonymous_variant | 0.14 |
Rv3236c | 3612704 | p.Glu138Ala | missense_variant | 0.12 |
Rv3236c | 3612719 | p.Ile133Thr | missense_variant | 0.13 |
alr | 3840410 | c.1010delG | frameshift_variant | 0.12 |
alr | 3841442 | c.-22G>A | upstream_gene_variant | 0.12 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.13 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4240767 | p.Arg302Leu | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243337 | c.105G>C | synonymous_variant | 0.12 |
embA | 4245065 | c.1833G>A | synonymous_variant | 0.17 |
embA | 4245875 | p.Lys881Asn | missense_variant | 0.2 |
embA | 4246192 | p.Phe987Ser | missense_variant | 0.11 |
embB | 4247111 | c.599delT | frameshift_variant | 0.11 |
aftB | 4267929 | p.Arg303Leu | missense_variant | 1.0 |
ubiA | 4269406 | p.Lys143Arg | missense_variant | 0.11 |
ethA | 4327064 | p.Cys137Tyr | missense_variant | 0.11 |
ethR | 4328024 | c.477delA | frameshift_variant | 0.12 |
whiB6 | 4338367 | p.Leu52Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |