Run ID: SRR1013527
Sample name:
Date: 02-04-2023 15:42:44
Number of reads: 252732
Percentage reads mapped: 3.54
Strain: lineage2.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
pncA | 2289080 | c.161delC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.75 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762030 | p.Thr742Ala | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.4 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.84 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.89 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.92 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.92 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.88 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.88 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.92 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.88 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.88 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.88 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.92 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.85 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.75 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.33 |
rpoC | 764616 | p.Asn416Ser | missense_variant | 0.44 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.67 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.67 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.53 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.27 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.87 |
rpoC | 764658 | c.1289_1290insTAC | disruptive_inframe_insertion | 0.27 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.82 |
rpoC | 764671 | c.1302G>A | synonymous_variant | 0.27 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 0.87 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.6 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.6 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.64 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.62 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.62 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.43 |
rpoC | 764890 | p.Leu507Phe | missense_variant | 0.18 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.5 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.53 |
rpoC | 764912 | p.Met515Val | missense_variant | 0.5 |
rpoC | 764918 | p.Val517Ile | missense_variant | 0.56 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.62 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.62 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 0.57 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.57 |
rpoC | 764958 | p.Glu530Ala | missense_variant | 0.57 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.57 |
rpoC | 764995 | c.1626C>T | synonymous_variant | 0.33 |
rpoC | 764998 | c.1629G>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.9 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472279 | n.434T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472606 | n.761C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475787 | n.2130C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | 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 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.25 |
ald | 3086739 | c.-81G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448670 | p.Asp56Ala | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641589 | p.Gly19Trp | missense_variant | 0.2 |
rpoA | 3878252 | c.253_255dupGTG | conservative_inframe_insertion | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269391 | p.Val148Ala | missense_variant | 0.8 |
ethA | 4326743 | p.Leu244Pro | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |