Run ID: SRR18911120
Sample name:
Date: 03-04-2023 20:40:37
Number of reads: 141299
Percentage reads mapped: 96.33
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154494 | c.1617delC | frameshift_variant | 0.29 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6023 | p.Lys262Glu | missense_variant | 0.25 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6418 | c.-884C>T | upstream_gene_variant | 0.2 |
gyrB | 6980 | p.Ala581Thr | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
rpoB | 759689 | c.-118A>G | upstream_gene_variant | 0.29 |
rpoB | 759708 | c.-99G>A | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765338 | p.Gln657Glu | missense_variant | 0.29 |
rpoC | 766621 | c.3253delC | frameshift_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303160 | p.Gly77Glu | missense_variant | 0.29 |
fbiC | 1304339 | p.Phe470Ser | missense_variant | 0.22 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406834 | c.507C>T | synonymous_variant | 0.67 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
atpE | 1461003 | c.-42A>G | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471752 | n.-94G>T | upstream_gene_variant | 0.33 |
rrs | 1472291 | n.446G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472398 | n.553T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475597 | n.1940G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.4 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
tlyA | 1918441 | p.Val168Phe | missense_variant | 0.25 |
ndh | 2102380 | c.663G>T | synonymous_variant | 0.33 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.6 |
katG | 2154049 | p.Lys688Met | missense_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155230 | p.Glu294Asp | missense_variant | 0.33 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288767 | p.Leu159Met | missense_variant | 0.67 |
pncA | 2288927 | c.315C>A | synonymous_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.75 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.67 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.67 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
ribD | 2987381 | p.Gln181His | missense_variant | 0.25 |
Rv2752c | 3065176 | p.Ser339* | stop_gained | 0.5 |
Rv2752c | 3065262 | p.Glu310Asp | missense_variant | 0.33 |
Rv2752c | 3065802 | p.Glu130Asp | missense_variant | 1.0 |
Rv2752c | 3066997 | c.-809_-807delTCG | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640597 | p.Val19Ile | missense_variant | 0.2 |
ddn | 3986734 | c.-109delT | upstream_gene_variant | 0.4 |
ddn | 3986745 | c.-98delG | upstream_gene_variant | 0.22 |
ddn | 3987127 | p.Asn95Thr | missense_variant | 0.29 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.29 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247639 | p.Ala376Thr | missense_variant | 0.25 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4326226 | c.1248C>A | synonymous_variant | 0.29 |
ethR | 4327435 | c.-114T>A | upstream_gene_variant | 0.22 |
ethA | 4327452 | p.Val8Ile | missense_variant | 0.25 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |