Run ID: SRR13861202
Sample name:
Date: 03-04-2023 09:25:54
Number of reads: 640121
Percentage reads mapped: 16.02
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 | 0.25 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6667 | p.Gln476His | missense_variant | 1.0 |
gyrA | 7289 | c.-13_-12insT | upstream_gene_variant | 1.0 |
rpoB | 760214 | p.Asn136Lys | missense_variant | 1.0 |
rpoB | 761126 | c.1320G>T | synonymous_variant | 0.24 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.25 |
rpoB | 761133 | p.Leu443Ile | missense_variant | 0.24 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.21 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.21 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.2 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.2 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.2 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.2 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.19 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.19 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.19 |
rpoB | 761196 | p.Leu464Phe | missense_variant | 0.2 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.22 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.22 |
rpoB | 761213 | c.1407G>A | synonymous_variant | 0.21 |
rpoB | 761220 | p.Ser472Thr | missense_variant | 0.19 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.19 |
rpoB | 761235 | p.Met477Val | missense_variant | 0.19 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.13 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.13 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.11 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.11 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.11 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.11 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.11 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.11 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
fbiC | 1304005 | p.Pro359Ser | missense_variant | 1.0 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473370 | n.1525T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.23 |
fabG1 | 1673813 | p.Arg125Leu | missense_variant | 1.0 |
inhA | 1674784 | p.Arg195Gly | missense_variant | 1.0 |
ndh | 2101793 | p.Trp417* | stop_gained | 0.93 |
PPE35 | 2169624 | p.Gly330Asp | missense_variant | 1.0 |
kasA | 2519223 | p.Thr370Ile | missense_variant | 1.0 |
ahpC | 2726213 | c.21C>T | synonymous_variant | 1.0 |
ribD | 2987016 | p.Gly60Arg | missense_variant | 1.0 |
Rv2752c | 3065644 | p.Thr183Ser | missense_variant | 1.0 |
thyA | 3074595 | c.-124C>A | upstream_gene_variant | 1.0 |
alr | 3841581 | c.-161T>A | upstream_gene_variant | 1.0 |
embC | 4242810 | p.Leu983Gln | missense_variant | 1.0 |
embB | 4246553 | p.Arg14Trp | missense_variant | 1.0 |
embB | 4248920 | p.Val803Met | missense_variant | 1.0 |
embB | 4249551 | p.Arg1013Leu | missense_variant | 1.0 |
ethA | 4326296 | p.Leu393Gln | missense_variant | 1.0 |