Run ID: ERR2514920
Sample name:
Date: 31-03-2023 20:38:35
Number of reads: 514613
Percentage reads mapped: 96.61
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 | 0.99 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.99 |
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 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575433 | p.Gly29Asp | missense_variant | 0.17 |
mshA | 575920 | c.573C>T | synonymous_variant | 0.33 |
ccsA | 619904 | p.His5Arg | missense_variant | 0.25 |
ccsA | 620701 | p.Ala271Thr | missense_variant | 0.2 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.38 |
rpoB | 761219 | c.1413G>T | synonymous_variant | 0.13 |
rpoB | 761771 | p.Met655Ile | missense_variant | 0.13 |
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 | 764653 | c.1284G>A | synonymous_variant | 0.17 |
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 | 777001 | p.His494Tyr | missense_variant | 0.22 |
mmpL5 | 777026 | c.1455C>T | synonymous_variant | 0.22 |
mmpL5 | 777760 | p.Leu241Phe | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781887 | p.Arg110Cys | missense_variant | 0.11 |
rplC | 800711 | c.-98C>T | upstream_gene_variant | 0.14 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.27 |
Rv1258c | 1407377 | c.-37C>A | upstream_gene_variant | 0.13 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417176 | p.Ala58Ser | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834195 | c.654G>A | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101701 | c.1342C>T | synonymous_variant | 0.22 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.33 |
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 | 2168904 | p.Ile570Thr | missense_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289922 | c.-681C>T | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2714147 | p.Val396Ile | missense_variant | 0.15 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726612 | c.420C>T | synonymous_variant | 0.13 |
folC | 2747639 | c.-41C>G | upstream_gene_variant | 0.25 |
pepQ | 2860161 | c.258G>A | synonymous_variant | 0.12 |
ribD | 2987000 | c.162C>G | synonymous_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065655 | c.537C>T | synonymous_variant | 1.0 |
Rv2752c | 3065784 | c.408C>T | synonymous_variant | 0.17 |
Rv2752c | 3066383 | c.-192T>C | upstream_gene_variant | 0.2 |
thyA | 3074256 | c.216G>T | synonymous_variant | 0.22 |
ald | 3086667 | c.-153_-152insG | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087378 | p.Ala187Thr | missense_variant | 0.12 |
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 |
whiB7 | 3568507 | p.Gln58Arg | missense_variant | 1.0 |
whiB7 | 3568593 | c.87C>T | synonymous_variant | 0.17 |
fbiA | 3640389 | c.-154C>A | upstream_gene_variant | 0.14 |
fbiB | 3640545 | c.-990G>A | upstream_gene_variant | 0.14 |
fbiB | 3642362 | c.828C>T | synonymous_variant | 0.2 |
alr | 3840328 | c.1093T>C | synonymous_variant | 0.14 |
clpC1 | 4038475 | p.Ser744Gly | missense_variant | 0.22 |
clpC1 | 4040217 | p.Gly163Val | missense_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4043974 | p.Pro103Leu | missense_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.17 |
embC | 4242614 | p.Ala918Ser | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243822 | p.Thr197Met | missense_variant | 0.18 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248241 | c.1728C>A | synonymous_variant | 0.15 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327197 | p.Gly93Arg | missense_variant | 0.25 |
ethA | 4328001 | c.-528G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 0.71 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338702 | c.-181T>A | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408050 | c.152delA | frameshift_variant | 0.2 |