Run ID: ERR4815800
Sample name:
Date: 01-04-2023 14:04:22
Number of reads: 1639561
Percentage reads mapped: 96.09
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.64 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6363 | c.1127delG | frameshift_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.1 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.11 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.11 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.11 |
rpoB | 763016 | p.Met1070Ile | missense_variant | 0.17 |
rpoC | 763432 | p.Arg21Ser | missense_variant | 0.15 |
rpoC | 763569 | p.Arg67Pro | missense_variant | 0.13 |
rpoC | 765262 | c.1895delA | frameshift_variant | 0.12 |
rpoC | 765649 | p.Phe760Leu | missense_variant | 0.11 |
rpoC | 766057 | c.2688C>T | synonymous_variant | 0.18 |
rpoC | 766508 | p.Ala1047Ser | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776531 | c.1950G>A | synonymous_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800863 | c.58delA | frameshift_variant | 0.15 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.13 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.13 |
embR | 1416259 | c.1089G>C | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471891 | n.46C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472901 | n.1056T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473183 | n.1338A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1834735 | c.1194C>T | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168252 | c.2361G>A | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290226 | c.-985T>C | upstream_gene_variant | 0.1 |
kasA | 2518216 | c.102G>A | synonymous_variant | 0.11 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3236c | 3612318 | p.Arg267Cys | missense_variant | 0.1 |
Rv3236c | 3612529 | p.Phe196Leu | missense_variant | 0.12 |
fbiA | 3641287 | c.749delA | frameshift_variant | 0.1 |
clpC1 | 4039731 | p.Leu325Asn | missense_variant | 0.12 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 0.1 |
clpC1 | 4040084 | c.621C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267172 | c.1665C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448498 | c.-5_*1408del | transcript_ablation | 1.0 |