Run ID: ERR11068488
Sample name:
Date: 06-04-2023 14:40:32
Number of reads: 3969253
Percentage reads mapped: 99.64
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 |
ccsA | 619984 | c.94C>T | synonymous_variant | 0.12 |
rpoB | 760975 | p.Met390Thr | missense_variant | 1.0 |
rpoC | 763941 | p.Ala191Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304197 | p.Gly423Ser | missense_variant | 0.1 |
Rv1258c | 1407050 | c.291C>T | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475778 | n.2121G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475962 | n.2305G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918600 | p.His221Tyr | missense_variant | 0.11 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519099 | p.Ala329Thr | missense_variant | 0.17 |
folC | 2746620 | p.Arg327Trp | missense_variant | 0.17 |
pepQ | 2860002 | c.417G>A | synonymous_variant | 0.11 |
thyX | 3067469 | c.477C>T | synonymous_variant | 0.1 |
ald | 3086767 | c.-53A>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
clpC1 | 4040235 | p.Gly157Ala | missense_variant | 0.3 |
embC | 4242563 | p.Ala901Thr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244263 | p.Leu344Arg | missense_variant | 0.11 |
embA | 4244503 | c.1275delG | frameshift_variant | 0.11 |
embB | 4246536 | p.Arg8His | missense_variant | 0.11 |
embB | 4246590 | p.Thr26Met | missense_variant | 0.11 |
embB | 4247104 | c.591G>A | synonymous_variant | 0.12 |
embB | 4247890 | c.1377C>T | synonymous_variant | 0.1 |
aftB | 4267715 | c.1122G>A | synonymous_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 |