Run ID: SRR2101462
Sample name:
Date: 03-04-2023 23:44:02
Number of reads: 490939
Percentage reads mapped: 96.71
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289224 | p.Ile6Met | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 490901 | c.123delT | frameshift_variant | 0.12 |
mshA | 575761 | c.414C>T | synonymous_variant | 1.0 |
mshA | 576004 | c.657T>C | synonymous_variant | 0.12 |
rpoB | 759814 | p.Asp3Gly | missense_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779349 | c.-869C>A | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781502 | c.-58G>T | upstream_gene_variant | 1.0 |
fbiC | 1304534 | p.Leu535Ser | missense_variant | 0.12 |
embR | 1416772 | c.576C>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1833372 | c.-170C>T | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.5 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 0.33 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 0.33 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.67 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Ile | missense_variant | 0.67 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.57 |
PPE35 | 2169071 | c.1542A>G | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289166 | p.Ala26Ser | missense_variant | 0.12 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.4 |
embB | 4249591 | p.Asp1026Glu | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |