Run ID: SRR6896229
Sample name:
Date: 04-04-2023 17:59:33
Number of reads: 442639
Percentage reads mapped: 96.66
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289224 | p.Ile6Met | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6751 | c.-551G>T | upstream_gene_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9300 | p.Ala667Thr | missense_variant | 0.12 |
fgd1 | 490901 | c.123delT | frameshift_variant | 0.13 |
fgd1 | 491531 | p.Ala250Val | missense_variant | 0.11 |
mshA | 575761 | c.414C>T | synonymous_variant | 1.0 |
mshA | 576004 | c.657T>C | synonymous_variant | 0.14 |
rpoB | 759814 | p.Asp3Gly | missense_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.17 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.13 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.13 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.12 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.13 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.12 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.11 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779349 | c.-869C>A | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781502 | c.-58G>T | upstream_gene_variant | 1.0 |
fbiC | 1304534 | p.Leu535Ser | missense_variant | 0.12 |
embR | 1416772 | c.576C>A | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1833372 | c.-170C>T | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169041 | c.1572G>A | synonymous_variant | 0.25 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.44 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 0.29 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 0.29 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.71 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Ile | missense_variant | 0.71 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.71 |
PPE35 | 2169071 | c.1542A>G | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289166 | p.Ala26Ser | missense_variant | 0.13 |
ribD | 2987111 | p.Glu91Asp | missense_variant | 0.11 |
Rv2752c | 3064832 | p.Ala454Thr | missense_variant | 0.12 |
rpoA | 3877512 | c.996C>A | synonymous_variant | 0.1 |
embB | 4249591 | p.Asp1026Glu | missense_variant | 0.12 |
aftB | 4267480 | p.Pro453Thr | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |