Run ID: SRR11972213
Sample name:
Date: 03-04-2023 05:32:12
Number of reads: 538709
Percentage reads mapped: 98.52
Strain: lineage1.1.3.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 0.99 |
lineage1.1.3.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5117 | c.-123G>A | upstream_gene_variant | 0.5 |
gyrB | 5415 | p.Ala59Val | missense_variant | 0.12 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6478 | c.-824G>A | upstream_gene_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7415 | c.114C>A | synonymous_variant | 0.17 |
gyrA | 7434 | p.Arg45Cys | missense_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7852 | p.Gly184Asp | missense_variant | 0.13 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491104 | p.Gly108Arg | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761385 | p.Ala527Ser | missense_variant | 0.14 |
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 | 763922 | p.Glu185* | stop_gained | 0.17 |
rpoC | 764451 | p.Gly361Asp | missense_variant | 0.11 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777572 | c.909C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305427 | c.2497C>T | synonymous_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.2 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.18 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.18 |
PPE35 | 2170435 | p.Arg60Trp | missense_variant | 0.15 |
PPE35 | 2170509 | p.Ala35Val | missense_variant | 0.13 |
PPE35 | 2170628 | c.-16C>T | upstream_gene_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289403 | c.-162T>A | upstream_gene_variant | 0.14 |
pncA | 2289443 | c.-202C>T | upstream_gene_variant | 0.17 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518512 | p.Gly133Ala | missense_variant | 0.11 |
kasA | 2518948 | c.834G>A | synonymous_variant | 0.18 |
eis | 2715357 | c.-25G>A | upstream_gene_variant | 0.12 |
eis | 2715453 | c.-121C>T | upstream_gene_variant | 0.16 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3064722 | c.1469delC | frameshift_variant | 0.12 |
Rv2752c | 3067032 | c.-841C>T | upstream_gene_variant | 0.36 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448402 | c.-102C>A | upstream_gene_variant | 0.17 |
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 |
Rv3236c | 3612592 | p.Asp175Glu | missense_variant | 0.13 |
alr | 3840375 | p.Asp349Val | missense_variant | 0.11 |
alr | 3841253 | c.168C>T | synonymous_variant | 1.0 |
alr | 3841277 | c.144C>T | synonymous_variant | 1.0 |
rpoA | 3878586 | c.-79A>G | upstream_gene_variant | 0.56 |
rpoA | 3878613 | c.-113_-107delCAACCCA | upstream_gene_variant | 0.5 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240164 | p.Gly101Asp | missense_variant | 0.2 |
embC | 4240235 | p.Arg125Trp | missense_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.9 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242784 | c.-449G>C | upstream_gene_variant | 0.12 |
embA | 4243478 | c.246G>A | synonymous_variant | 0.15 |
embA | 4243557 | p.Ala109Thr | missense_variant | 0.18 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244217 | p.Thr329Ser | missense_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246098 | p.Phe956Ile | missense_variant | 0.13 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248341 | p.Thr610Ala | missense_variant | 0.11 |
embB | 4248504 | p.Asp664Val | missense_variant | 0.15 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326914 | p.Ala187Val | missense_variant | 0.15 |
ethR | 4327456 | c.-93G>A | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408239 | c.-37A>T | upstream_gene_variant | 0.12 |
whiB6 | 4338429 | c.-218_92del | frameshift_variant&start_lost | 1.0 |