Run ID: ERR495191
Sample name:
Date: 01-04-2023 21:41:36
Number of reads: 390659
Percentage reads mapped: 98.87
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 5581 | p.Tyr114* | stop_gained | 0.14 |
gyrB | 6077 | p.Gly280Cys | missense_variant | 0.17 |
gyrB | 6226 | p.Asn329Lys | missense_variant | 0.18 |
gyrB | 6833 | p.Asp532Asn | missense_variant | 0.18 |
gyrB | 7001 | p.Asp588Asn | missense_variant | 0.17 |
gyrB | 7201 | p.Glu654Asp | missense_variant | 0.4 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7832 | c.531G>A | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491463 | c.681G>A | synonymous_variant | 0.25 |
rpoB | 762082 | p.Gly759Asp | missense_variant | 0.4 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777396 | p.Ser362Asn | missense_variant | 0.2 |
mmpL5 | 777797 | c.684G>T | synonymous_variant | 0.4 |
mmpL5 | 778907 | c.-427C>T | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781544 | c.-16G>A | upstream_gene_variant | 0.25 |
fbiC | 1302945 | c.15A>G | synonymous_variant | 0.29 |
fbiC | 1305211 | p.Pro761Thr | missense_variant | 0.2 |
atpE | 1461263 | c.219G>T | synonymous_variant | 0.25 |
atpE | 1461289 | c.245A>T | stop_lost&splice_region_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471780 | n.-66G>T | upstream_gene_variant | 0.2 |
rrs | 1471787 | n.-59T>A | upstream_gene_variant | 0.22 |
rrs | 1471869 | n.24G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472186 | n.341C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.22 |
inhA | 1674690 | c.489C>T | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918560 | c.621G>A | synonymous_variant | 0.33 |
tlyA | 1918737 | c.798G>A | synonymous_variant | 0.22 |
ndh | 2101830 | p.Ile405Phe | missense_variant | 0.33 |
katG | 2155557 | c.555C>T | synonymous_variant | 0.2 |
PPE35 | 2168407 | c.2206C>T | synonymous_variant | 0.4 |
PPE35 | 2169428 | c.1185C>T | synonymous_variant | 0.29 |
Rv1979c | 2221726 | p.Thr480Ile | missense_variant | 0.29 |
Rv1979c | 2223264 | c.-100C>T | upstream_gene_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290062 | c.-821G>T | upstream_gene_variant | 0.25 |
pncA | 2290107 | c.-866T>A | upstream_gene_variant | 1.0 |
pncA | 2290113 | c.-872G>T | upstream_gene_variant | 0.29 |
pncA | 2290130 | c.-889C>T | upstream_gene_variant | 0.29 |
eis | 2714611 | p.Leu241Pro | missense_variant | 0.2 |
folC | 2746213 | c.1386G>A | synonymous_variant | 0.33 |
folC | 2746471 | c.1128C>A | synonymous_variant | 0.29 |
pepQ | 2859806 | p.His205Asn | missense_variant | 0.15 |
ribD | 2987295 | p.Arg153Cys | missense_variant | 0.25 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.5 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086867 | c.48G>T | synonymous_variant | 0.33 |
ald | 3087615 | p.Asp266Asn | missense_variant | 0.25 |
ald | 3087811 | p.Ala331Val | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568712 | c.-33C>T | upstream_gene_variant | 0.4 |
whiB7 | 3568817 | c.-138C>A | upstream_gene_variant | 0.4 |
Rv3236c | 3613104 | p.Arg5Trp | missense_variant | 0.2 |
fbiA | 3640358 | c.-184_-182delCAA | upstream_gene_variant | 0.4 |
fbiA | 3640364 | c.-179_-178insT | upstream_gene_variant | 0.4 |
fbiA | 3640930 | p.Glu130* | stop_gained | 0.2 |
fbiB | 3640986 | c.-549C>T | upstream_gene_variant | 0.29 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246755 | p.Ala81Asp | missense_variant | 0.67 |
embB | 4247350 | c.837C>A | synonymous_variant | 0.33 |
embB | 4248978 | p.Thr822Lys | missense_variant | 0.18 |
embB | 4249184 | p.Gly891Arg | missense_variant | 0.33 |
ubiA | 4269631 | p.Ala68Val | missense_variant | 0.22 |
ethA | 4326121 | c.1353G>A | synonymous_variant | 0.29 |
whiB6 | 4338365 | p.Cys53Arg | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408012 | p.Arg64Gln | missense_variant | 0.22 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |