Run ID: ERR4819871
Sample name:
Date: 01-04-2023 16:21:08
Number of reads: 1043883
Percentage reads mapped: 99.4
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 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779610 | c.-705T>C | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472301 | n.456C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472719 | n.874G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.12 |
PPE35 | 2167760 | c.2853G>A | synonymous_variant | 0.14 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.16 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.16 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.11 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.12 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.17 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.17 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.19 |
PPE35 | 2170412 | c.201G>T | synonymous_variant | 0.12 |
PPE35 | 2170415 | c.198A>C | synonymous_variant | 0.12 |
PPE35 | 2170454 | c.159C>G | synonymous_variant | 0.15 |
PPE35 | 2170457 | c.156G>C | synonymous_variant | 0.15 |
PPE35 | 2170460 | c.153G>A | synonymous_variant | 0.16 |
PPE35 | 2170465 | p.Ala50Ser | missense_variant | 0.16 |
PPE35 | 2170472 | c.141G>A | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519107 | p.Cys331* | stop_gained | 0.14 |
thyX | 3067451 | p.Lys165Asn | missense_variant | 0.11 |
fbiD | 3339196 | c.83delC | frameshift_variant | 0.12 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.12 |
Rv3236c | 3612574 | c.543G>A | synonymous_variant | 1.0 |
clpC1 | 4039530 | p.Asp392Ala | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.1 |
embB | 4247494 | c.981G>A | synonymous_variant | 1.0 |
aftB | 4267925 | c.912G>C | synonymous_variant | 0.2 |
aftB | 4268198 | p.Ile213Met | missense_variant | 1.0 |
ubiA | 4269864 | c.-31C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |