Run ID: SRR14088376
Sample name:
Date: 03-04-2023 09:46:20
Number of reads: 755461
Percentage reads mapped: 99.5
Strain: lineage3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761128 | p.Ser441Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5625 | c.387delC | frameshift_variant | 0.12 |
gyrB | 6737 | p.Thr500Ala | missense_variant | 1.0 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7958 | c.657C>T | synonymous_variant | 1.0 |
gyrA | 8282 | c.981G>T | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490908 | c.126G>A | synonymous_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619814 | c.-77G>T | upstream_gene_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.31 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760300 | p.Thr165Asn | missense_variant | 0.22 |
rpoB | 760461 | p.Arg219Cys | missense_variant | 0.22 |
rpoB | 760659 | p.Ser285Thr | missense_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775812 | p.Phe890Ala | missense_variant | 0.11 |
mmpL5 | 775817 | c.2664T>C | synonymous_variant | 0.11 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776265 | p.Lys739Arg | missense_variant | 1.0 |
mmpL5 | 778011 | p.Gln157Arg | missense_variant | 0.12 |
mmpR5 | 779186 | p.Gly66Val | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800888 | p.Thr27Asn | missense_variant | 0.17 |
embR | 1417457 | c.-110C>T | upstream_gene_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673606 | p.Phe56Ser | missense_variant | 0.1 |
rpsA | 1833515 | c.-27C>A | upstream_gene_variant | 0.12 |
rpsA | 1833909 | p.Asp123Gly | missense_variant | 0.33 |
rpsA | 1834985 | c.1445dupG | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101700 | p.Leu448Gln | missense_variant | 0.13 |
ndh | 2101702 | c.1341G>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156259 | c.-148T>C | upstream_gene_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168975 | c.1638C>G | synonymous_variant | 0.5 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 1.0 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 1.0 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.82 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.82 |
PPE35 | 2170627 | c.-15G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2222042 | p.Thr375Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289018 | c.218_223delTCAGCG | disruptive_inframe_deletion | 0.17 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518154 | p.Val14Leu | missense_variant | 0.15 |
kasA | 2518158 | p.Val15Glu | missense_variant | 0.17 |
eis | 2714566 | p.Leu256Pro | missense_variant | 0.15 |
eis | 2715050 | p.Gly95Arg | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2986748 | c.-91A>G | upstream_gene_variant | 0.11 |
ribD | 2987440 | p.Thr201Ile | missense_variant | 0.33 |
Rv2752c | 3065722 | p.Ala157Val | missense_variant | 0.22 |
Rv2752c | 3065983 | p.Arg70Gln | missense_variant | 0.17 |
thyA | 3074401 | p.Thr24Ile | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448441 | c.-63A>G | upstream_gene_variant | 0.22 |
Rv3083 | 3449217 | p.Trp238* | stop_gained | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474887 | p.Leu294Pro | missense_variant | 0.11 |
whiB7 | 3568473 | p.Glu69Asp | missense_variant | 0.2 |
fbiB | 3640584 | c.-951C>A | upstream_gene_variant | 0.4 |
alr | 3840497 | c.924G>A | synonymous_variant | 0.12 |
panD | 4044203 | p.Thr27Pro | missense_variant | 0.22 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244900 | c.1668G>A | synonymous_variant | 0.11 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.3 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.68 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.76 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.76 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.58 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.48 |
embB | 4249783 | c.3270A>G | synonymous_variant | 0.12 |
ethA | 4326079 | c.1395C>T | synonymous_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407732 | c.463_470delCCGAACGG | frameshift_variant | 1.0 |