Run ID: SRR19428551
Sample name:
Date: 03-04-2023 21:39:54
Number of reads: 405367
Percentage reads mapped: 99.61
Strain: lineage4;lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.88 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.05 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 0.53 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.83 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8665 | c.1366delG | frameshift_variant | 0.11 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.96 |
mshA | 576077 | c.730C>T | synonymous_variant | 0.2 |
mshA | 576183 | c.837dupA | frameshift_variant | 0.11 |
ccsA | 620351 | p.Arg154His | missense_variant | 0.1 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.6 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.88 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.24 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.24 |
rpoC | 764509 | c.1140G>T | synonymous_variant | 0.12 |
rpoC | 766796 | c.3428delG | frameshift_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776409 | p.Leu691Pro | missense_variant | 0.1 |
mmpL5 | 776685 | p.Ser599Leu | missense_variant | 0.1 |
mmpL5 | 777607 | p.Gly292Ser | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.12 |
fbiC | 1304173 | p.Val415Met | missense_variant | 0.17 |
fbiC | 1304422 | p.Ala498Thr | missense_variant | 0.13 |
fbiC | 1305112 | p.Asp728Asn | missense_variant | 0.12 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.15 |
Rv1258c | 1406349 | p.Ile331Ser | missense_variant | 0.63 |
Rv1258c | 1407208 | p.Ser45Pro | missense_variant | 0.11 |
Rv1258c | 1407363 | c.-23C>T | upstream_gene_variant | 0.11 |
embR | 1416577 | c.771G>A | synonymous_variant | 0.11 |
embR | 1417153 | c.195C>A | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476471 | n.2814G>A | non_coding_transcript_exon_variant | 0.1 |
inhA | 1674762 | c.561T>C | synonymous_variant | 0.2 |
inhA | 1674902 | p.Asp234Gly | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101703 | p.Glu447Val | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.75 |
pncA | 2289105 | p.Ala46Gly | missense_variant | 0.12 |
pncA | 2289325 | c.-84T>G | upstream_gene_variant | 0.12 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.83 |
pncA | 2289969 | c.-728G>A | upstream_gene_variant | 0.12 |
kasA | 2519083 | c.969C>A | synonymous_variant | 0.15 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.77 |
Rv2752c | 3065711 | p.Gly161Ser | missense_variant | 0.14 |
Rv2752c | 3067008 | c.-817C>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339741 | c.624G>A | synonymous_variant | 0.2 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.1 |
Rv3083 | 3448944 | c.441G>C | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.17 |
fprA | 3474605 | p.Arg200Gln | missense_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.1 |
fbiA | 3641219 | p.Val226Ala | missense_variant | 0.12 |
fbiB | 3641304 | c.-231C>A | upstream_gene_variant | 0.1 |
fbiB | 3641914 | p.Ala127Asp | missense_variant | 0.11 |
alr | 3840461 | c.960G>T | synonymous_variant | 0.14 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.18 |
panD | 4044204 | c.78G>A | synonymous_variant | 0.12 |
embC | 4240068 | p.Ser69Asn | missense_variant | 0.12 |
embC | 4240953 | p.Ile364Thr | missense_variant | 0.11 |
embC | 4241562 | p.Arg567His | missense_variant | 0.94 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.82 |
embC | 4242503 | p.Pro881Thr | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.17 |
embA | 4243528 | p.Asp99Gly | missense_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.29 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.94 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.19 |