Run ID: ERR4821915
Sample name:
Date: 01-04-2023 17:31:26
Number of reads: 128112
Percentage reads mapped: 64.02
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.88 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.36 | streptomycin |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491343 | c.561C>T | synonymous_variant | 0.67 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575446 | c.99A>C | synonymous_variant | 0.33 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.67 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.67 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.67 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.67 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.67 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.5 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.5 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.6 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.6 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.6 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.75 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.75 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.75 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.67 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.67 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.67 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.67 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.75 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.67 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.6 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.5 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.5 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.5 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.5 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.4 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.4 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 778477 | c.429A>G | stop_lost&splice_region_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406242 | p.Ala367Thr | missense_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473293 | n.1449A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918104 | c.165G>A | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
eis | 2715218 | p.Leu39Met | missense_variant | 0.29 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449736 | c.1233G>T | synonymous_variant | 0.4 |
fbiA | 3640421 | c.-122C>T | upstream_gene_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326093 | p.Tyr461Asp | missense_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407892 | p.Met104Lys | missense_variant | 1.0 |