Run ID: SRR6896545
Sample name:
Date: 04-04-2023 18:09:23
Number of reads: 34071
Percentage reads mapped: 77.13
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 | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.4 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 6307 | c.-995T>C | upstream_gene_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 760774 | p.Thr323Lys | missense_variant | 0.67 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.4 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.4 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.4 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.5 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.4 |
rpoC | 762980 | c.-390T>A | upstream_gene_variant | 0.4 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 1.0 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 1.0 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rplC | 800888 | p.Thr27Asn | missense_variant | 0.29 |
Rv1258c | 1407155 | c.186C>A | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474711 | n.1054_1055insAA | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.5 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.5 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.5 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.5 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.5 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.5 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.5 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 0.29 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.33 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.33 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.33 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 0.33 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.33 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.33 |
rpsA | 1833794 | p.Glu85Thr | missense_variant | 0.33 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.33 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.33 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.33 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.33 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.33 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.33 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.33 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.33 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.5 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.5 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.67 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.67 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.67 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.67 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.67 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.57 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.57 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.57 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.57 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.5 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.5 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.5 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.38 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.57 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.57 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.57 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.57 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.57 |
rpsA | 1834398 | p.His286Leu | missense_variant | 0.57 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.57 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.57 |
rpsA | 1834418 | p.Ile293Leu | missense_variant | 0.57 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.57 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.57 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.5 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.5 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.5 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.5 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.5 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.6 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.5 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.4 |
katG | 2154128 | p.Leu662Ile | missense_variant | 1.0 |
katG | 2154183 | c.1929G>A | synonymous_variant | 1.0 |
katG | 2156043 | c.69G>A | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289025 | p.Val73Phe | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |