Run ID: SRR5818430
Sample name:
Date: 04-04-2023 11:27:10
Number of reads: 203047
Percentage reads mapped: 98.6
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 |
---|---|---|---|---|
gyrA | 6454 | c.-848C>T | upstream_gene_variant | 0.99 |
gyrA | 6721 | c.-581C>T | upstream_gene_variant | 0.98 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7665 | p.Asp122Asn | missense_variant | 0.2 |
mmpL5 | 779283 | c.-803G>A | upstream_gene_variant | 0.85 |
mmpL5 | 779295 | c.-815A>G | upstream_gene_variant | 0.83 |
mmpR5 | 779431 | p.Asn148Gln | missense_variant | 0.88 |
mmpL5 | 779472 | c.-992G>A | upstream_gene_variant | 0.85 |
mmpS5 | 779523 | c.-618T>A | upstream_gene_variant | 0.8 |
mmpS5 | 779538 | c.-633A>C | upstream_gene_variant | 1.0 |
mmpS5 | 779539 | c.-634C>A | upstream_gene_variant | 1.0 |
rplC | 801267 | c.459A>G | synonymous_variant | 0.99 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.23 |
inhA | 1674816 | c.615T>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155345 | p.Ala256Val | missense_variant | 0.15 |
pncA | 2289104 | c.138A>G | synonymous_variant | 0.95 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.5 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.22 |
embB | 4247590 | c.1077A>G | synonymous_variant | 0.92 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.93 |
embB | 4247815 | c.1302C>T | synonymous_variant | 0.95 |
ethA | 4326463 | c.1011C>T | synonymous_variant | 1.0 |
ethA | 4326740 | p.Arg245His | missense_variant | 1.0 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.5 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |