Run ID: SRR6046907
Sample name:
Date: 04-04-2023 12:25:19
Number of reads: 20303
Percentage reads mapped: 38.89
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5217 | c.-23C>A | upstream_gene_variant | 1.0 |
gyrA | 8869 | p.Thr523Lys | missense_variant | 1.0 |
mshA | 576757 | c.1410C>A | synonymous_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.5 |
Rv1258c | 1406245 | c.1096C>T | synonymous_variant | 1.0 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472911 | n.1066T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472915 | n.1070G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472918 | n.1073A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474186 | n.529A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>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 |
Rv2752c | 3066278 | c.-87C>A | upstream_gene_variant | 1.0 |
embC | 4241330 | p.Asp490Asn | missense_variant | 0.5 |
embC | 4242118 | c.2256C>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4268084 | c.753G>A | synonymous_variant | 1.0 |
ethA | 4327325 | p.Tyr50Phe | missense_variant | 1.0 |
ethA | 4328338 | c.-865G>A | upstream_gene_variant | 1.0 |