Run ID: SRR13861662
Sample name:
Date: 03-04-2023 09:37:27
Number of reads: 51478
Percentage reads mapped: 2.58
Strain: lineage4.9
Drug-resistance: RR-TB
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 |
---|---|---|---|---|---|
rpoB | 761131 | p.Gly442Glu | missense_variant | 0.75 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 761126 | c.1320G>T | synonymous_variant | 1.0 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.75 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.75 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.75 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.75 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.75 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.6 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.6 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.4 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.6 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.6 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.6 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.6 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.6 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.6 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.6 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.6 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.6 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.6 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.5 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.75 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.75 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.75 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.75 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.75 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.75 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.75 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.75 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.75 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.75 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.75 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.6 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.75 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.75 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.75 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.75 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.75 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.75 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.75 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.75 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.75 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
kasA | 2518301 | p.His63Asp | missense_variant | 1.0 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
Rv3083 | 3449104 | p.Pro201Ala | missense_variant | 1.0 |
fbiB | 3641723 | c.189T>C | synonymous_variant | 1.0 |
rpoA | 3877740 | c.768G>T | synonymous_variant | 1.0 |