Run ID: ERR9117838
Sample name:
Date: 02-04-2023 09:32:54
Number of reads: 1073348
Percentage reads mapped: 99.26
Strain: lineage1.1.2
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 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | 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 | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrB | 6547 | c.1310delG | frameshift_variant | 0.14 |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575504 | p.His53Tyr | missense_variant | 0.17 |
mshA | 575730 | p.Gln128Pro | missense_variant | 0.11 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.27 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.27 |
ccsA | 620753 | p.Arg288Leu | missense_variant | 0.14 |
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 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304419 | p.Ala497Thr | missense_variant | 1.0 |
fbiC | 1304474 | p.Leu515Pro | missense_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674875 | p.Arg225Leu | missense_variant | 0.4 |
rpsA | 1834575 | p.Met345Thr | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154911 | p.Pro401Thr | missense_variant | 0.12 |
katG | 2155845 | c.267G>A | synonymous_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290136 | c.-895C>T | upstream_gene_variant | 1.0 |
pncA | 2290182 | c.-941G>C | upstream_gene_variant | 0.11 |
kasA | 2518123 | c.9G>A | synonymous_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715557 | c.-225C>T | upstream_gene_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746828 | c.771C>T | synonymous_variant | 0.13 |
pepQ | 2859489 | c.930C>G | synonymous_variant | 0.11 |
pepQ | 2860011 | p.Asp136Glu | missense_variant | 0.14 |
Rv2752c | 3064558 | p.Tyr545Cys | missense_variant | 0.17 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3064983 | c.1209G>A | synonymous_variant | 0.12 |
thyX | 3067208 | c.738G>A | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449178 | p.Lys225Asn | missense_variant | 0.12 |
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 | 3612922 | c.195T>G | synonymous_variant | 0.11 |
Rv3236c | 3613016 | p.Pro34Gln | missense_variant | 1.0 |
fbiA | 3640398 | c.-145G>C | upstream_gene_variant | 1.0 |
fbiB | 3641921 | c.387C>T | synonymous_variant | 0.2 |
alr | 3841138 | p.Asp95Asn | missense_variant | 1.0 |
alr | 3841200 | p.Ala74Gly | missense_variant | 0.11 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240625 | p.Asp255Asn | missense_variant | 0.14 |
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 | 4243138 | c.-95C>A | upstream_gene_variant | 0.12 |
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 | 4246508 | c.-6G>C | upstream_gene_variant | 0.11 |
embB | 4247070 | p.Val186Asp | missense_variant | 0.12 |
embB | 4247620 | c.1107G>T | synonymous_variant | 0.2 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268915 | c.-79C>T | upstream_gene_variant | 0.13 |
ubiA | 4268941 | p.Ala298Val | missense_variant | 0.14 |
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 |
ethA | 4328392 | c.-919C>A | upstream_gene_variant | 0.12 |
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 |
gid | 4408291 | c.-89C>T | upstream_gene_variant | 0.13 |