Run ID: ERR9882583
Sample name:
Date: 02-04-2023 13:25:46
Number of reads: 738710
Percentage reads mapped: 97.24
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
fgd1 | 491648 | p.Asp289Gly | missense_variant | 0.12 |
rpoC | 763647 | p.Gly93Asp | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474989 | n.1332_1333insA | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.15 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.11 |
pncA | 2289735 | c.-494C>G | upstream_gene_variant | 0.13 |
kasA | 2519057 | p.Thr315Ser | missense_variant | 0.13 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.12 |
kasA | 2519065 | c.951C>A | synonymous_variant | 0.12 |
kasA | 2519066 | c.956_982delACGCCGCGGAGGCCAACGCCATCCGCG | disruptive_inframe_deletion | 0.14 |
folC | 2747361 | p.Arg80Cys | missense_variant | 0.11 |
thyA | 3074052 | c.420G>T | synonymous_variant | 0.12 |
Rv3083 | 3449137 | c.634C>A | synonymous_variant | 0.15 |
whiB7 | 3568875 | c.-196C>T | upstream_gene_variant | 0.11 |
embC | 4243082 | c.3221_3228delATCTGAAC | frameshift_variant | 0.11 |
embC | 4243092 | p.Leu1077Arg | missense_variant | 0.11 |
embC | 4243095 | p.Gly1078Val | missense_variant | 0.11 |
embA | 4243099 | c.-134G>C | upstream_gene_variant | 0.11 |
embA | 4243102 | c.-131G>T | upstream_gene_variant | 0.11 |
embC | 4243103 | p.Thr1081Pro | missense_variant | 0.11 |
embC | 4243106 | p.Arg1082Ser | missense_variant | 0.11 |
embC | 4243107 | c.3245_3246insGTTCAGAT | frameshift_variant | 0.11 |
embA | 4244185 | p.Ser318Ile | missense_variant | 0.12 |
embB | 4246578 | p.Ser22Tyr | missense_variant | 0.12 |
embB | 4246617 | p.Leu35Pro | missense_variant | 0.11 |
embB | 4248765 | p.Asp751Gly | missense_variant | 0.1 |