Run ID: ERR3324330
Sample name:
Date: 01-04-2023 01:49:48
Number of reads: 2063393
Percentage reads mapped: 99.19
Strain: lineage5.1.1;lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.92 |
lineage5 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.1 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.85 |
lineage5.1 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.1 |
lineage5.1.1 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 0.08 |
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 | 0.23 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406402 | c.939C>G | synonymous_variant | 0.88 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.85 |
inhA | 1673338 | c.-864G>A | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101840 | c.1203G>A | synonymous_variant | 0.17 |
ndh | 2101921 | c.1122G>A | synonymous_variant | 0.25 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.18 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.81 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290062 | c.-821G>A | upstream_gene_variant | 0.23 |
Rv3083 | 3449248 | p.Ala249Ser | missense_variant | 0.2 |
Rv3083 | 3449644 | p.Ala381Thr | missense_variant | 0.79 |
Rv3083 | 3449723 | p.Cys407Phe | missense_variant | 0.18 |
Rv3083 | 3449735 | p.Arg411Leu | missense_variant | 0.17 |
Rv3083 | 3449832 | c.1329T>C | synonymous_variant | 0.11 |
Rv3083 | 3449883 | p.Trp460Cys | missense_variant | 0.12 |
alr | 3840932 | c.489C>T | synonymous_variant | 0.14 |
rpoA | 3878493 | c.15G>A | synonymous_variant | 0.13 |
rpoA | 3878573 | c.-66G>T | upstream_gene_variant | 0.15 |
ddn | 3986987 | c.144G>T | synonymous_variant | 0.16 |
ddn | 3987180 | p.Asp113Asn | missense_variant | 0.19 |
embC | 4239843 | c.-20A>C | upstream_gene_variant | 0.1 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 0.14 |
aftB | 4268050 | p.Pro263Thr | missense_variant | 0.81 |
ethR | 4326928 | c.-621G>A | upstream_gene_variant | 0.18 |
ethA | 4327103 | p.Gly124Asp | missense_variant | 0.18 |
whiB6 | 4338547 | c.-26A>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.1 |
gid | 4407790 | p.Ala138Val | missense_variant | 0.8 |