Run ID: ERR4821901
Sample name:
Date: 01-04-2023 17:31:03
Number of reads: 477664
Percentage reads mapped: 98.84
Strain: lineage1.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.99 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.99 |
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 | 5346 | p.Ser36Leu | missense_variant | 0.5 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
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 | 8233 | p.Gly311Asp | missense_variant | 0.18 |
gyrA | 8414 | p.Asp371Glu | missense_variant | 0.67 |
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 | 9803 | c.2502C>T | synonymous_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.75 |
ccsA | 620108 | p.Asp73Gly | missense_variant | 0.33 |
rpoB | 760785 | p.Leu327Val | missense_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763150 | p.Phe1115Ser | missense_variant | 0.33 |
rpoC | 763826 | p.Ala153Thr | missense_variant | 0.13 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 766358 | p.Ile997Val | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776158 | p.Asp775His | missense_variant | 0.2 |
mmpL5 | 778404 | p.Arg26Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303803 | c.873C>A | synonymous_variant | 0.25 |
Rv1258c | 1406173 | p.Thr390Ala | missense_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417449 | c.-102C>T | upstream_gene_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834035 | c.495delC | frameshift_variant | 0.2 |
rpsA | 1834853 | p.Ala438Thr | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
ndh | 2102380 | c.663G>T | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155574 | p.Thr180Ala | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2170713 | c.-101A>G | upstream_gene_variant | 0.2 |
Rv1979c | 2221957 | p.Glu403Gly | missense_variant | 1.0 |
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 |
kasA | 2518612 | c.498C>G | synonymous_variant | 0.25 |
eis | 2714468 | p.Trp289Arg | missense_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747118 | p.Ala161Ser | missense_variant | 0.18 |
folC | 2747614 | c.-16G>A | upstream_gene_variant | 0.25 |
pepQ | 2859755 | p.Phe222Leu | missense_variant | 0.12 |
pepQ | 2860239 | p.Tyr60* | stop_gained | 0.14 |
ribD | 2987161 | p.Ala108Asp | missense_variant | 0.15 |
Rv2752c | 3065516 | p.Ile226Val | missense_variant | 0.5 |
Rv2752c | 3066115 | p.Glu26Gly | missense_variant | 0.29 |
Rv2752c | 3066222 | c.-32delG | upstream_gene_variant | 0.22 |
thyX | 3067308 | p.Ile213Asn | missense_variant | 0.15 |
thyA | 3074002 | p.Gly157Asp | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087601 | p.Gly261Val | missense_variant | 1.0 |
fbiD | 3339243 | p.Met42Ile | missense_variant | 0.11 |
fbiD | 3339525 | c.408G>A | synonymous_variant | 0.29 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449748 | c.1245C>T | synonymous_variant | 0.11 |
Rv3083 | 3449867 | p.Gly455Val | missense_variant | 0.17 |
Rv3083 | 3449968 | c.1468delC | frameshift_variant | 0.29 |
fprA | 3473837 | c.-169delG | upstream_gene_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474208 | c.206delA | frameshift_variant | 0.2 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474890 | p.Val295Ala | missense_variant | 0.13 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3613109 | p.Val3Ala | missense_variant | 0.18 |
fbiA | 3641099 | c.561delT | frameshift_variant | 0.2 |
fbiB | 3641813 | c.279G>A | synonymous_variant | 0.18 |
fbiB | 3642496 | p.Leu321His | missense_variant | 0.13 |
alr | 3840859 | p.Val188Ile | missense_variant | 0.12 |
rpoA | 3877943 | p.Phe189Leu | missense_variant | 0.2 |
clpC1 | 4038437 | p.Lys756Asn | missense_variant | 0.15 |
clpC1 | 4039052 | c.1652delT | frameshift_variant | 0.22 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_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 |
embA | 4246323 | p.Leu1031Met | missense_variant | 0.15 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269562 | p.Pro91Gln | missense_variant | 0.29 |
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 |
ethA | 4326840 | p.Ile212Val | missense_variant | 0.4 |
ethA | 4328322 | c.-850_-849insT | upstream_gene_variant | 0.5 |
whiB6 | 4338199 | p.Asp108Val | missense_variant | 0.22 |
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 | 4407803 | c.399delT | frameshift_variant | 1.0 |
gid | 4407808 | p.Asp132Ala | missense_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408457 | c.-255A>G | upstream_gene_variant | 0.4 |