Run ID: ERR2229016
Sample name:
Date: 31-03-2023 16:30:26
Number of reads: 324672
Percentage reads mapped: 99.59
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 | 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 | 8271 | p.Ala324Thr | missense_variant | 0.12 |
ccsA | 620238 | c.348G>A | synonymous_variant | 0.15 |
rpoC | 765215 | p.Ala616Thr | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406568 | p.Val258Glu | missense_variant | 0.2 |
embR | 1417040 | p.Leu103Arg | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.94 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474912 | n.1256delT | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475459 | n.1802C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476610 | n.2953C>T | non_coding_transcript_exon_variant | 0.22 |
inhA | 1673601 | c.-601G>T | upstream_gene_variant | 0.33 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155053 | p.Tyr353* | stop_gained | 0.33 |
katG | 2155092 | c.1020G>A | synonymous_variant | 0.33 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.27 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168981 | c.1632A>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288702 | c.540C>T | synonymous_variant | 0.18 |
pncA | 2289882 | c.-641C>A | upstream_gene_variant | 0.17 |
pncA | 2290191 | c.-950C>A | upstream_gene_variant | 0.33 |
pncA | 2290213 | c.-972G>T | upstream_gene_variant | 0.4 |
kasA | 2518435 | c.321G>A | synonymous_variant | 0.29 |
Rv2752c | 3066160 | p.Leu11Pro | missense_variant | 0.25 |
ald | 3087865 | p.Ala349Val | missense_variant | 0.17 |
fbiB | 3642658 | p.Val375Gly | missense_variant | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.14 |
clpC1 | 4038509 | c.2196C>T | synonymous_variant | 0.29 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326984 | p.Pro164Thr | missense_variant | 0.15 |
ethA | 4327336 | p.Asp46Glu | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |