Run ID: ERR4819839
Sample name:
Date: 01-04-2023 16:19:59
Number of reads: 200587
Percentage reads mapped: 98.03
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5311 | c.72G>A | synonymous_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrB | 6642 | p.Lys468Arg | missense_variant | 0.33 |
gyrB | 6752 | p.Ile505Val | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7612 | p.Ser104Leu | missense_variant | 0.4 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.2 |
gyrA | 9242 | c.1941A>G | synonymous_variant | 0.22 |
gyrA | 9251 | c.1950G>C | synonymous_variant | 0.29 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.29 |
gyrA | 9263 | c.1962C>T | synonymous_variant | 0.33 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.22 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.2 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.25 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.25 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.25 |
gyrA | 9329 | c.2028C>G | synonymous_variant | 0.29 |
gyrA | 9508 | p.Ala736Val | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
ccsA | 620503 | p.Glu205Lys | missense_variant | 0.25 |
rpoB | 760119 | p.Arg105Cys | missense_variant | 0.29 |
rpoB | 760261 | p.Pro152Leu | missense_variant | 0.22 |
rpoB | 760490 | c.684C>T | 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 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 766749 | p.Pro1127Leu | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778046 | c.-944C>T | upstream_gene_variant | 0.12 |
mmpL5 | 778056 | p.Ser142Thr | missense_variant | 0.14 |
mmpR5 | 778061 | c.-929C>T | upstream_gene_variant | 0.15 |
mmpL5 | 778064 | p.Ala139Ser | missense_variant | 0.17 |
mmpL5 | 778072 | p.Thr137Ala | missense_variant | 0.18 |
mmpR5 | 778073 | c.-917G>C | upstream_gene_variant | 0.18 |
mmpR5 | 778082 | c.-908T>C | upstream_gene_variant | 0.22 |
mmpR5 | 778088 | c.-902C>G | upstream_gene_variant | 0.22 |
mmpL5 | 779148 | c.-668C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302809 | c.-122A>G | upstream_gene_variant | 0.5 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673392 | c.-48G>T | upstream_gene_variant | 0.17 |
fabG1 | 1673608 | p.Gly57Ser | missense_variant | 0.5 |
inhA | 1674311 | p.Val37Ala | missense_variant | 0.67 |
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 | 2169479 | c.1134C>T | synonymous_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2714573 | c.759delG | frameshift_variant | 0.33 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747038 | c.561C>T | synonymous_variant | 0.25 |
pepQ | 2859495 | p.Ile308Met | missense_variant | 0.67 |
ribD | 2986663 | c.-176C>T | upstream_gene_variant | 0.22 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyA | 3074595 | c.-124C>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086955 | p.Thr46Ala | missense_variant | 0.33 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474207 | c.201C>T | synonymous_variant | 0.29 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612005 | p.Arg371His | missense_variant | 0.29 |
fbiA | 3640582 | p.Arg14Ser | missense_variant | 0.18 |
fbiB | 3642320 | c.786C>T | synonymous_variant | 0.25 |
fbiB | 3642612 | p.Tyr360His | missense_variant | 0.5 |
alr | 3840856 | c.565C>A | synonymous_variant | 0.33 |
rpoA | 3878372 | p.Ile46Phe | missense_variant | 0.33 |
clpC1 | 4039331 | c.1374C>A | synonymous_variant | 0.22 |
clpC1 | 4039428 | p.Glu426Val | missense_variant | 0.67 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040669 | c.36C>T | synonymous_variant | 0.25 |
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 | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245218 | c.1986C>T | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.17 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.18 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.18 |
ubiA | 4269031 | p.Gly268Asp | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269961 | c.-128C>G | upstream_gene_variant | 0.4 |
ethA | 4328302 | c.-829C>G | upstream_gene_variant | 0.18 |
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 | 4407701 | p.His168Tyr | missense_variant | 0.18 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408009 | p.Val65Ala | missense_variant | 0.18 |