Run ID: ERR036248
Sample name:
Date: 31-03-2023 08:32:00
Number of reads: 6587602
Percentage reads mapped: 99.54
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.92 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.07 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.32 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777399 | p.Thr361Arg | missense_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800997 | p.Asn63Lys | missense_variant | 0.3 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.24 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474380 | n.723G>T | non_coding_transcript_exon_variant | 0.31 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.28 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.95 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.18 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.35 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.22 |
eis | 2714787 | p.Trp182* | stop_gained | 0.93 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.4 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.17 |
Rv2752c | 3064552 | p.Arg547Pro | missense_variant | 0.2 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.25 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.22 |
ald | 3086750 | c.-70A>C | upstream_gene_variant | 0.87 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.11 |
fbiD | 3339550 | p.Gly145Trp | missense_variant | 0.29 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 0.5 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 0.41 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 0.24 |
Rv3083 | 3449882 | p.Trp460* | stop_gained | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 0.13 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.18 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.31 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.92 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.23 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.22 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.24 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.33 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.16 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |