Run ID: SRR12199395
Sample name:
Date: 03-04-2023 06:37:10
Number of reads: 298513
Percentage reads mapped: 94.57
Strain: lineage1.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.99 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6960 | p.Gln574Arg | missense_variant | 0.9 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
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 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9406 | p.Gly702Asp | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
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 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777256 | p.Pro409Thr | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416311 | p.Ser346Leu | missense_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472619 | n.774C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472620 | n.775A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.3 |
inhA | 1674619 | p.Pro140Ala | missense_variant | 1.0 |
rpsA | 1833353 | c.-189C>A | upstream_gene_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918555 | p.Arg206Trp | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169220 | c.1393C>T | synonymous_variant | 0.33 |
PPE35 | 2169237 | p.Asp459Gly | missense_variant | 0.4 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.25 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.25 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.59 |
PPE35 | 2170528 | p.Ser29Ala | missense_variant | 0.25 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ribD | 2986713 | c.-126A>C | upstream_gene_variant | 0.29 |
ribD | 2987150 | p.Gln104His | missense_variant | 0.4 |
Rv2752c | 3065354 | p.Arg280* | stop_gained | 0.17 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_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 |
Rv3236c | 3612883 | c.234T>C | synonymous_variant | 0.33 |
fbiA | 3640375 | c.-168C>A | upstream_gene_variant | 0.22 |
rpoA | 3877595 | p.Gly305Ser | missense_variant | 0.29 |
rpoA | 3877698 | p.His270Gln | missense_variant | 0.2 |
rpoA | 3877722 | c.786C>T | synonymous_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.2 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.2 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248160 | c.1647C>T | synonymous_variant | 0.25 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |