Run ID: ERR2513581
Sample name:
Date: 31-03-2023 19:46:29
Number of reads: 470378
Percentage reads mapped: 99.23
Strain: lineage1.1.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.99 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.1 | Indo-Oceanic | EAI4;EAI5 | RD239 | 0.99 |
lineage1.1.1.1 | Indo-Oceanic | EAI4;ZERO | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6343 | p.Glu368Asp | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8227 | p.Arg309Gln | missense_variant | 0.14 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.43 |
fgd1 | 490972 | p.Arg64Ser | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.36 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575806 | c.459G>T | synonymous_variant | 0.12 |
mshA | 576416 | p.Leu357Met | missense_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.88 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.88 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776089 | p.Val798Ile | missense_variant | 0.18 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776766 | p.Ala572Val | missense_variant | 0.17 |
mmpL5 | 777351 | p.Arg377Leu | missense_variant | 0.29 |
mmpL5 | 777581 | p.Tyr300* | stop_gained | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.22 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.36 |
fbiC | 1303303 | p.Pro125Thr | missense_variant | 0.13 |
embR | 1416401 | p.Asn316Ser | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474709 | n.1052G>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673474 | p.Pro12Leu | missense_variant | 0.22 |
rpsA | 1833360 | c.-182G>A | upstream_gene_variant | 0.29 |
rpsA | 1834319 | p.Val260Ile | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918289 | p.Gln117Arg | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156389 | c.-278G>C | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168270 | c.2343G>C | synonymous_variant | 0.13 |
PPE35 | 2169293 | c.1320T>G | synonymous_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.29 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222439 | c.726C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290221 | c.-980C>A | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyA | 3074030 | p.Ala148Thr | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087035 | c.216C>A | synonymous_variant | 0.12 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449527 | p.Ile342Phe | missense_variant | 0.14 |
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 | 3568540 | p.Pro47Leu | missense_variant | 0.17 |
whiB7 | 3568742 | c.-63C>A | upstream_gene_variant | 0.15 |
fbiB | 3642029 | c.495C>A | synonymous_variant | 0.17 |
rpoA | 3877599 | p.Gln303His | missense_variant | 0.15 |
clpC1 | 4038420 | p.Arg762Leu | missense_variant | 0.15 |
clpC1 | 4040350 | p.Val119Leu | missense_variant | 0.15 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240766 | c.904C>A | synonymous_variant | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.29 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244096 | c.864C>T | synonymous_variant | 0.92 |
embA | 4244720 | c.1488C>T | synonymous_variant | 1.0 |
embA | 4244879 | c.1647C>G | synonymous_variant | 1.0 |
embA | 4245761 | p.Tyr843* | stop_gained | 0.22 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.94 |
embB | 4248112 | c.1599C>T | synonymous_variant | 0.14 |
embB | 4248848 | p.Pro779Ser | missense_variant | 0.12 |
aftB | 4268013 | p.Pro275Gln | missense_variant | 0.17 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
aftB | 4269609 | c.-773G>A | upstream_gene_variant | 0.14 |
ubiA | 4269663 | p.Met57Ile | missense_variant | 0.13 |
ethA | 4326212 | p.Arg421Gln | missense_variant | 0.11 |
ethA | 4326452 | p.Ala341Glu | missense_variant | 0.12 |
whiB6 | 4338242 | p.Gln94Glu | 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 |