Run ID: ERR2245356
Sample name:
Date: 31-03-2023 17:39:22
Number of reads: 1613233
Percentage reads mapped: 99.29
Strain: lineage3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326160 | p.Tyr438* | stop_gained | 0.12 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5481 | p.Gly81Asp | missense_variant | 0.17 |
gyrB | 5523 | p.Thr95Asn | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8701 | p.Asp467Gly | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491162 | p.Glu127Val | missense_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575752 | c.405G>T | synonymous_variant | 0.14 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
ccsA | 619920 | c.30G>T | synonymous_variant | 0.22 |
ccsA | 620423 | p.Val178Ala | missense_variant | 0.11 |
rpoB | 759681 | c.-126C>T | upstream_gene_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760002 | p.Glu66Lys | missense_variant | 0.12 |
rpoB | 760915 | p.Arg370His | missense_variant | 0.17 |
rpoB | 760997 | c.1191G>T | synonymous_variant | 0.25 |
rpoB | 762119 | c.2313C>T | synonymous_variant | 0.2 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.95 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763771 | p.Tyr134* | stop_gained | 0.17 |
rpoC | 765589 | c.2220G>A | synonymous_variant | 0.2 |
rpoC | 766519 | c.3150C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775856 | c.2625T>G | synonymous_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776609 | p.Met624Ile | missense_variant | 0.17 |
mmpL5 | 777684 | p.Leu266Pro | missense_variant | 0.14 |
mmpR5 | 778292 | c.-698C>T | upstream_gene_variant | 0.12 |
mmpR5 | 779077 | p.Arg30Trp | missense_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1460969 | c.-76G>T | upstream_gene_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471718 | n.-128G>T | upstream_gene_variant | 0.18 |
rrs | 1471898 | n.53A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473546 | n.-112G>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102105 | p.Gly313Ala | missense_variant | 0.2 |
ndh | 2102184 | c.859A>C | synonymous_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167819 | p.Gly932Cys | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168269 | p.Gly782Cys | missense_variant | 0.22 |
PPE35 | 2168674 | p.Asn647Asp | missense_variant | 0.11 |
PPE35 | 2168843 | c.1770G>T | synonymous_variant | 0.18 |
PPE35 | 2168890 | p.Ala575Ser | missense_variant | 0.17 |
PPE35 | 2169029 | p.Asp528Glu | missense_variant | 0.18 |
PPE35 | 2169063 | p.Met517Lys | missense_variant | 0.2 |
PPE35 | 2169157 | p.Thr486Pro | missense_variant | 0.2 |
PPE35 | 2170310 | c.303G>T | synonymous_variant | 0.12 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2222419 | p.Asp249Ala | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289041 | c.201G>A | synonymous_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2517977 | c.-138C>T | upstream_gene_variant | 0.12 |
kasA | 2518717 | c.603C>A | synonymous_variant | 0.17 |
eis | 2714152 | p.Val394Ala | missense_variant | 0.22 |
eis | 2714633 | p.Lys234Glu | missense_variant | 0.12 |
eis | 2714883 | p.His150Gln | missense_variant | 0.22 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746477 | c.1122T>C | synonymous_variant | 0.15 |
folC | 2746712 | p.Glu296Val | missense_variant | 0.18 |
folC | 2746792 | p.Gln269His | missense_variant | 0.13 |
folC | 2746996 | c.603C>T | synonymous_variant | 0.12 |
ribD | 2986776 | c.-63C>T | upstream_gene_variant | 0.12 |
Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.1 |
Rv2752c | 3065541 | p.Glu217Asp | missense_variant | 0.18 |
Rv2752c | 3065977 | p.Asp72Gly | missense_variant | 0.5 |
thyA | 3074094 | c.378G>T | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087232 | p.Gly138Asp | missense_variant | 0.12 |
Rv3083 | 3448307 | c.-197T>G | upstream_gene_variant | 0.17 |
Rv3083 | 3448378 | c.-126C>A | upstream_gene_variant | 0.13 |
Rv3083 | 3448509 | p.Asn2Lys | missense_variant | 0.2 |
Rv3083 | 3448588 | p.Asp29Tyr | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474903 | c.897C>T | synonymous_variant | 0.13 |
whiB7 | 3568661 | p.Pro7Ser | missense_variant | 0.18 |
Rv3236c | 3612295 | p.Phe274Leu | missense_variant | 0.12 |
Rv3236c | 3613190 | c.-74A>G | upstream_gene_variant | 0.2 |
fbiB | 3641361 | c.-174C>T | upstream_gene_variant | 0.15 |
fbiA | 3641506 | p.Ala322Thr | missense_variant | 0.14 |
fbiB | 3642692 | c.1158C>T | synonymous_variant | 0.13 |
alr | 3840243 | p.Ser393Ile | missense_variant | 0.13 |
alr | 3840604 | p.Pro273Ser | missense_variant | 0.18 |
clpC1 | 4038786 | p.Gln640Leu | missense_variant | 0.29 |
clpC1 | 4040036 | c.669C>A | synonymous_variant | 0.17 |
clpC1 | 4040249 | p.Glu152Gly | missense_variant | 0.18 |
panD | 4044275 | p.Arg3Trp | missense_variant | 0.14 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4240376 | c.515delT | frameshift_variant | 0.17 |
embC | 4240810 | p.Trp316* | stop_gained | 0.22 |
embC | 4241502 | p.Ser547* | stop_gained | 0.2 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4241795 | p.Asn645His | missense_variant | 0.15 |
embC | 4241909 | p.Ala683Ser | missense_variant | 0.18 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242103 | p.Lys747Asn | missense_variant | 0.18 |
embC | 4242164 | p.Pro768Thr | missense_variant | 0.14 |
embC | 4242286 | p.Phe808Leu | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243259 | c.27T>C | synonymous_variant | 0.18 |
embA | 4244362 | p.Asn377Thr | missense_variant | 0.2 |
embA | 4244606 | c.1374G>A | synonymous_variant | 0.17 |
embA | 4244937 | p.Lys569* | stop_gained | 0.18 |
embA | 4245204 | p.Gly658Arg | missense_variant | 0.17 |
embA | 4245723 | p.Gly831* | stop_gained | 0.13 |
embA | 4246039 | p.Ala936Asp | missense_variant | 0.2 |
embA | 4246377 | p.Asp1049Tyr | missense_variant | 0.17 |
embB | 4247028 | p.Leu172Gln | missense_variant | 0.18 |
embB | 4247303 | p.Gly264Ser | missense_variant | 0.13 |
embB | 4249521 | p.Ala1003Asp | missense_variant | 0.15 |
embB | 4249659 | p.Met1049Lys | missense_variant | 0.18 |
aftB | 4268089 | p.Trp250Arg | missense_variant | 0.11 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.21 |
ethA | 4327563 | c.-90C>T | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |