Run ID: ERR5866434
Sample name:
Date: 02-04-2023 00:41:09
Number of reads: 408330
Percentage reads mapped: 99.69
Strain: lineage4.8
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.18 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
gid | 4407896 | p.Glu103* | stop_gained | 0.93 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5465 | p.Glu76* | stop_gained | 0.27 |
gyrB | 5722 | c.483G>T | synonymous_variant | 0.3 |
gyrB | 6159 | c.923_925delTCA | disruptive_inframe_deletion | 0.2 |
gyrA | 7189 | c.-113C>A | upstream_gene_variant | 0.18 |
gyrA | 7283 | c.-19G>T | upstream_gene_variant | 0.2 |
gyrA | 7307 | c.6A>G | synonymous_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7400 | p.Met33Ile | missense_variant | 0.5 |
gyrA | 7424 | c.123G>T | synonymous_variant | 0.33 |
gyrA | 7953 | p.Ala218Ser | missense_variant | 0.15 |
gyrA | 9091 | p.Ala597Val | missense_variant | 0.18 |
gyrA | 9248 | c.1947G>T | synonymous_variant | 0.15 |
gyrA | 9251 | c.1950G>T | synonymous_variant | 0.15 |
gyrA | 9608 | p.Asp769Glu | missense_variant | 0.13 |
gyrA | 9809 | c.2508G>T | synonymous_variant | 0.18 |
fgd1 | 490589 | c.-194G>T | upstream_gene_variant | 0.18 |
fgd1 | 490819 | p.Glu13* | stop_gained | 0.29 |
fgd1 | 490936 | p.Pro52Thr | missense_variant | 0.25 |
fgd1 | 491119 | p.Glu113* | stop_gained | 0.18 |
fgd1 | 491307 | c.525C>A | synonymous_variant | 0.15 |
fgd1 | 491322 | c.540G>A | synonymous_variant | 0.17 |
fgd1 | 491723 | p.Gly314Val | missense_variant | 0.22 |
mshA | 575435 | p.Pro30Thr | missense_variant | 0.15 |
mshA | 575492 | p.Leu49Met | missense_variant | 0.25 |
mshA | 575954 | p.Glu203* | stop_gained | 0.25 |
mshA | 576248 | p.Pro301Thr | missense_variant | 0.12 |
mshA | 576382 | c.1035G>T | synonymous_variant | 0.2 |
mshA | 576419 | p.Val358Phe | missense_variant | 0.22 |
mshA | 576674 | p.Arg443Ser | missense_variant | 0.25 |
ccsA | 619720 | c.-171C>A | upstream_gene_variant | 0.22 |
ccsA | 619949 | p.Ser20* | stop_gained | 0.33 |
ccsA | 620045 | p.Gly52Val | missense_variant | 0.25 |
ccsA | 620095 | p.His69Asn | missense_variant | 0.22 |
ccsA | 620717 | p.Ala276Val | missense_variant | 0.17 |
rpoB | 761205 | p.Arg467Ser | missense_variant | 0.15 |
rpoB | 761533 | p.Ser576* | stop_gained | 0.22 |
rpoB | 761632 | p.Ala609Glu | missense_variant | 0.18 |
rpoB | 761730 | p.Gly642Cys | missense_variant | 0.18 |
rpoB | 761852 | c.2046C>A | synonymous_variant | 0.4 |
rpoB | 761939 | p.Lys711Asn | missense_variant | 0.29 |
rpoB | 761998 | p.Leu731Pro | missense_variant | 1.0 |
rpoB | 762275 | c.2469C>A | synonymous_variant | 0.14 |
rpoC | 762470 | c.-900G>T | upstream_gene_variant | 0.4 |
rpoB | 762559 | p.Arg918Leu | missense_variant | 0.25 |
rpoB | 762609 | p.His935Tyr | missense_variant | 0.25 |
rpoC | 763968 | p.Gly200Val | missense_variant | 0.17 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.4 |
rpoC | 764665 | c.1296C>A | synonymous_variant | 0.22 |
rpoC | 764714 | p.Leu449Met | missense_variant | 0.17 |
rpoC | 765404 | p.Leu679Met | missense_variant | 0.18 |
rpoC | 765611 | p.His748Asn | missense_variant | 0.15 |
rpoC | 765813 | p.Arg815Leu | missense_variant | 0.33 |
rpoC | 767089 | p.Cys1240* | stop_gained | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775668 | p.Trp938Leu | missense_variant | 0.18 |
mmpL5 | 775681 | p.Gly934* | stop_gained | 0.15 |
mmpL5 | 775778 | c.2703C>A | synonymous_variant | 0.15 |
mmpL5 | 775914 | p.Ala856Asp | missense_variant | 0.25 |
mmpL5 | 776087 | c.2394C>A | synonymous_variant | 0.5 |
mmpL5 | 777245 | c.1236G>T | synonymous_variant | 0.25 |
mmpL5 | 777749 | c.732C>T | synonymous_variant | 0.16 |
mmpR5 | 778445 | c.-545G>T | upstream_gene_variant | 0.2 |
mmpS5 | 778613 | p.Ser98Tyr | missense_variant | 0.27 |
mmpL5 | 779064 | c.-584G>T | upstream_gene_variant | 0.17 |
mmpR5 | 779095 | p.Ala36Ser | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781479 | c.-81G>T | upstream_gene_variant | 0.19 |
rpsL | 781745 | p.Glu62Asp | missense_variant | 0.15 |
rpsL | 781792 | p.Ser78* | stop_gained | 0.18 |
rpsL | 781813 | p.Gly85Asp | missense_variant | 0.17 |
rplC | 800771 | c.-38C>A | upstream_gene_variant | 0.17 |
rplC | 800976 | p.Glu56Asp | missense_variant | 0.17 |
rplC | 801186 | c.378C>A | synonymous_variant | 0.17 |
fbiC | 1302782 | c.-149C>A | upstream_gene_variant | 0.25 |
fbiC | 1302811 | c.-120G>A | upstream_gene_variant | 0.15 |
fbiC | 1302823 | c.-108G>T | upstream_gene_variant | 0.15 |
fbiC | 1302825 | c.-106C>A | upstream_gene_variant | 0.15 |
fbiC | 1302937 | p.Gln3Lys | missense_variant | 0.2 |
fbiC | 1304512 | p.Val528Ile | missense_variant | 0.15 |
fbiC | 1304682 | c.1752C>A | synonymous_variant | 0.23 |
fbiC | 1304722 | p.Glu598* | stop_gained | 0.18 |
Rv1258c | 1407057 | p.Gly95Val | missense_variant | 0.15 |
Rv1258c | 1407338 | c.3G>T | start_lost | 0.4 |
Rv1258c | 1407386 | c.-46C>A | upstream_gene_variant | 0.4 |
embR | 1417191 | p.Asp53Tyr | missense_variant | 0.25 |
atpE | 1461089 | c.45G>T | synonymous_variant | 0.18 |
atpE | 1461278 | c.234A>G | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472562 | n.717C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473011 | n.1166G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473196 | n.1351C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473203 | n.1358G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474083 | n.426C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474262 | n.605C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474778 | n.1121C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474873 | n.1217delA | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475596 | n.1939G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475690 | n.2033G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476513 | n.2856G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476725 | n.3068C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476756 | n.3099G>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673180 | c.-260C>A | upstream_gene_variant | 0.2 |
fabG1 | 1673231 | c.-209G>A | upstream_gene_variant | 0.18 |
fabG1 | 1673588 | p.Gly50Glu | missense_variant | 0.22 |
fabG1 | 1673650 | p.Ala71Ser | missense_variant | 0.17 |
fabG1 | 1674066 | p.Lys209Asn | missense_variant | 0.22 |
inhA | 1674328 | c.127C>A | synonymous_variant | 0.29 |
inhA | 1674507 | c.306G>T | synonymous_variant | 0.4 |
inhA | 1674637 | p.Gly146Cys | missense_variant | 0.17 |
rpsA | 1833504 | c.-38_-37insC | upstream_gene_variant | 0.2 |
rpsA | 1833539 | c.-2_-1delAT | upstream_gene_variant | 0.18 |
rpsA | 1834986 | c.1445G>T | stop_lost&splice_region_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918046 | p.Gly36Val | missense_variant | 0.15 |
tlyA | 1918182 | c.243G>A | synonymous_variant | 0.22 |
tlyA | 1918276 | p.Val113Ile | missense_variant | 0.22 |
tlyA | 1918378 | p.Arg147Ser | missense_variant | 0.25 |
tlyA | 1918495 | p.Glu186* | stop_gained | 0.29 |
tlyA | 1918548 | p.Leu203Phe | missense_variant | 0.29 |
tlyA | 1918703 | p.Gly255Val | missense_variant | 0.33 |
ndh | 2102152 | c.891C>A | synonymous_variant | 0.18 |
ndh | 2102732 | p.Leu104Pro | missense_variant | 0.11 |
ndh | 2103023 | p.Pro7His | missense_variant | 0.18 |
katG | 2154926 | p.Arg396Ser | missense_variant | 0.33 |
katG | 2155115 | p.Leu333Ile | missense_variant | 0.25 |
katG | 2155569 | c.543C>T | synonymous_variant | 0.22 |
katG | 2155659 | c.453C>A | synonymous_variant | 0.25 |
katG | 2155704 | p.Pro136Ser | missense_variant | 0.2 |
katG | 2155772 | p.Arg114Ser | missense_variant | 0.25 |
katG | 2156372 | c.-261C>A | upstream_gene_variant | 0.2 |
katG | 2156376 | c.-265C>A | upstream_gene_variant | 0.22 |
PPE35 | 2167860 | p.Gly918Val | missense_variant | 0.17 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2168176 | p.Gln813Lys | missense_variant | 0.3 |
PPE35 | 2168442 | p.Trp724Leu | missense_variant | 0.15 |
PPE35 | 2170367 | p.Gln82His | missense_variant | 0.2 |
PPE35 | 2170663 | c.-51G>T | upstream_gene_variant | 0.17 |
Rv1979c | 2222375 | p.Gly264Cys | missense_variant | 0.2 |
Rv1979c | 2222448 | c.717G>T | synonymous_variant | 0.33 |
Rv1979c | 2222499 | c.666G>T | synonymous_variant | 0.17 |
Rv1979c | 2222701 | p.Gly155Val | missense_variant | 0.2 |
Rv1979c | 2222837 | p.Ala110Ser | missense_variant | 0.17 |
Rv1979c | 2223259 | c.-95C>A | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288822 | c.420C>A | synonymous_variant | 0.15 |
pncA | 2289175 | p.Gly23Cys | missense_variant | 0.22 |
pncA | 2289339 | c.-98C>A | upstream_gene_variant | 0.18 |
pncA | 2289549 | c.-308G>T | upstream_gene_variant | 0.19 |
pncA | 2289655 | c.-414G>T | upstream_gene_variant | 0.29 |
kasA | 2517936 | c.-179G>T | upstream_gene_variant | 0.29 |
kasA | 2518074 | c.-41G>T | upstream_gene_variant | 0.22 |
kasA | 2518101 | c.-14G>T | upstream_gene_variant | 0.22 |
kasA | 2518193 | p.Pro27Ser | missense_variant | 0.22 |
kasA | 2518216 | p.Lys34Asn | missense_variant | 0.18 |
kasA | 2518323 | p.Ser70Ile | missense_variant | 0.18 |
kasA | 2518329 | c.218delG | frameshift_variant | 0.2 |
kasA | 2518356 | p.Ser81Leu | missense_variant | 0.17 |
kasA | 2518513 | c.399C>A | synonymous_variant | 0.15 |
kasA | 2519069 | p.Asp319Tyr | missense_variant | 0.25 |
ahpC | 2726192 | c.-1C>A | upstream_gene_variant | 0.19 |
folC | 2746211 | p.Arg463Ile | missense_variant | 0.2 |
folC | 2746265 | p.Ser445* | stop_gained | 0.25 |
folC | 2746452 | p.Gly383Cys | missense_variant | 0.15 |
folC | 2746797 | c.802C>A | synonymous_variant | 0.2 |
folC | 2746918 | c.681G>T | synonymous_variant | 0.2 |
folC | 2747596 | c.3G>T | start_lost | 0.22 |
folC | 2747630 | c.-32G>T | upstream_gene_variant | 0.18 |
pepQ | 2859322 | p.Pro366His | missense_variant | 0.15 |
pepQ | 2859343 | p.Pro359Gln | missense_variant | 0.17 |
pepQ | 2859500 | p.Gly307Cys | missense_variant | 0.29 |
pepQ | 2859776 | p.Gly215Cys | missense_variant | 0.25 |
pepQ | 2860155 | c.264C>A | synonymous_variant | 0.3 |
pepQ | 2860166 | p.Gly85Ser | missense_variant | 0.2 |
ribD | 2986826 | c.-13T>C | upstream_gene_variant | 0.14 |
ribD | 2987032 | p.Pro65His | missense_variant | 0.15 |
ribD | 2987426 | c.588G>T | synonymous_variant | 0.29 |
ribD | 2987609 | p.Lys257Asn | missense_variant | 0.22 |
Rv2752c | 3064647 | c.1545G>T | synonymous_variant | 0.15 |
Rv2752c | 3066006 | c.186G>T | synonymous_variant | 0.18 |
Rv2752c | 3066102 | p.Asn30Lys | missense_variant | 0.13 |
thyA | 3074064 | c.408C>A | synonymous_variant | 0.17 |
thyA | 3074382 | p.Phe30Leu | missense_variant | 0.22 |
thyA | 3074394 | c.78C>A | synonymous_variant | 0.2 |
ald | 3086958 | p.Asp47Asn | missense_variant | 0.17 |
ald | 3087716 | c.897G>T | synonymous_variant | 0.29 |
fbiD | 3338979 | c.-139G>T | upstream_gene_variant | 0.22 |
fbiD | 3339305 | p.Thr63Asn | missense_variant | 0.21 |
fbiD | 3339310 | p.Asp65Asn | missense_variant | 0.17 |
fbiD | 3339317 | p.Ala67Val | missense_variant | 0.17 |
fbiD | 3339335 | p.Ala73Val | missense_variant | 0.14 |
fbiD | 3339580 | p.Gly155Cys | missense_variant | 0.18 |
Rv3083 | 3448328 | c.-176G>A | upstream_gene_variant | 0.5 |
fprA | 3473862 | c.-145C>A | upstream_gene_variant | 0.18 |
fprA | 3473949 | c.-58G>T | upstream_gene_variant | 0.4 |
fprA | 3474193 | p.Ile63Val | missense_variant | 0.2 |
fprA | 3474218 | p.Ala71Gly | missense_variant | 0.18 |
fprA | 3474900 | c.894C>A | synonymous_variant | 0.4 |
fprA | 3475050 | c.1044C>A | synonymous_variant | 0.25 |
fprA | 3475104 | c.1098G>A | synonymous_variant | 0.15 |
whiB7 | 3568729 | c.-50G>T | upstream_gene_variant | 0.17 |
whiB7 | 3568778 | c.-99C>A | upstream_gene_variant | 0.27 |
whiB7 | 3568810 | c.-131G>A | upstream_gene_variant | 0.22 |
Rv3236c | 3611982 | p.Ala379Ser | missense_variant | 0.18 |
Rv3236c | 3612421 | c.696G>T | synonymous_variant | 0.18 |
Rv3236c | 3613175 | c.-59G>T | upstream_gene_variant | 0.2 |
Rv3236c | 3613229 | c.-113G>T | upstream_gene_variant | 0.17 |
fbiA | 3640400 | c.-143G>T | upstream_gene_variant | 0.2 |
fbiA | 3640417 | c.-126C>A | upstream_gene_variant | 0.14 |
fbiA | 3641479 | p.Pro313Thr | missense_variant | 0.22 |
fbiB | 3641559 | p.Ala9Ser | missense_variant | 0.18 |
fbiB | 3641640 | p.Ala36Ser | missense_variant | 0.2 |
fbiB | 3642039 | p.Gly169Cys | missense_variant | 0.25 |
fbiB | 3642714 | p.Gly394Cys | missense_variant | 0.17 |
alr | 3840464 | p.Phe319Leu | missense_variant | 0.17 |
rpoA | 3878409 | c.99C>A | synonymous_variant | 0.14 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
panD | 4044057 | c.225C>A | synonymous_variant | 0.22 |
panD | 4044122 | c.160C>A | synonymous_variant | 0.18 |
panD | 4044174 | c.108C>T | synonymous_variant | 0.22 |
panD | 4044297 | c.-16C>A | upstream_gene_variant | 0.18 |
panD | 4044325 | c.-44C>A | upstream_gene_variant | 0.2 |
embC | 4239949 | c.87C>T | synonymous_variant | 0.22 |
embC | 4239989 | p.Leu43Met | missense_variant | 0.18 |
embC | 4240089 | p.Gly76Val | missense_variant | 0.17 |
embC | 4240465 | p.Phe201Leu | missense_variant | 0.2 |
embC | 4240485 | p.Ala208Glu | missense_variant | 0.18 |
embC | 4240506 | p.Ser215* | stop_gained | 0.2 |
embC | 4241054 | p.Pro398Thr | missense_variant | 0.25 |
embC | 4241069 | p.Ala403Thr | missense_variant | 0.25 |
embC | 4241388 | p.Ser509Ile | missense_variant | 0.18 |
embC | 4241431 | p.Phe523Leu | missense_variant | 0.25 |
embC | 4241455 | c.1593C>A | synonymous_variant | 0.33 |
embC | 4241490 | p.Ala543Glu | missense_variant | 0.17 |
embC | 4241777 | p.Gly639Cys | missense_variant | 0.22 |
embC | 4241808 | p.Pro649Gln | missense_variant | 0.17 |
embA | 4242313 | c.-920C>A | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243410 | c.182delC | frameshift_variant | 0.2 |
embA | 4243574 | c.342C>A | synonymous_variant | 0.29 |
embA | 4243785 | p.Leu185Met | missense_variant | 0.17 |
embA | 4243808 | p.Asp192Glu | missense_variant | 0.18 |
embA | 4244859 | p.Gly543Trp | missense_variant | 0.18 |
embA | 4245508 | p.Gly759Val | missense_variant | 0.33 |
embA | 4245582 | p.Asp784Tyr | missense_variant | 0.38 |
embA | 4246047 | p.Ala939Thr | missense_variant | 0.25 |
embA | 4246279 | p.Ala1016Val | missense_variant | 0.2 |
embA | 4246396 | p.Gly1055Val | missense_variant | 0.18 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.22 |
embB | 4246849 | p.Gln112His | missense_variant | 0.33 |
embB | 4247005 | c.492C>A | synonymous_variant | 0.22 |
embB | 4247125 | c.612G>T | synonymous_variant | 0.22 |
embB | 4247632 | c.1119C>A | synonymous_variant | 0.18 |
embB | 4247890 | c.1377C>A | synonymous_variant | 0.17 |
embB | 4247999 | p.Asp496Tyr | missense_variant | 0.18 |
embB | 4248343 | c.1830G>T | synonymous_variant | 0.18 |
embB | 4249109 | p.Pro866Thr | missense_variant | 0.15 |
aftB | 4266978 | p.Gly620Val | missense_variant | 0.2 |
aftB | 4267183 | p.Gly552Cys | missense_variant | 0.4 |
aftB | 4267354 | p.Gly495Cys | missense_variant | 0.2 |
aftB | 4267586 | c.1251C>A | synonymous_variant | 0.29 |
aftB | 4267634 | c.1203G>T | synonymous_variant | 0.22 |
aftB | 4268254 | p.Leu195Met | missense_variant | 0.18 |
aftB | 4268903 | c.-68delC | upstream_gene_variant | 0.25 |
aftB | 4269012 | c.-176G>T | upstream_gene_variant | 0.17 |
ubiA | 4269484 | p.Ala117Val | missense_variant | 0.15 |
ubiA | 4269648 | p.Phe62Leu | missense_variant | 0.22 |
aftB | 4269804 | c.-968G>T | upstream_gene_variant | 0.15 |
ethA | 4326224 | p.Val417Ala | missense_variant | 0.1 |
ethA | 4326326 | p.Thr383Met | missense_variant | 0.15 |
ethA | 4326418 | c.1056G>T | synonymous_variant | 0.18 |
ethA | 4326483 | p.Arg331Ser | missense_variant | 0.22 |
ethA | 4326657 | p.Pro273Ser | missense_variant | 0.2 |
ethA | 4326897 | p.Ala193Ser | missense_variant | 0.22 |
ethA | 4327216 | p.Lys86Asn | missense_variant | 0.17 |
ethR | 4327228 | c.-321G>T | upstream_gene_variant | 0.2 |
ethA | 4327257 | p.Gln73Lys | missense_variant | 0.2 |
ethR | 4327882 | p.Glu112Gln | missense_variant | 0.13 |
gid | 4407698 | p.Asp169Tyr | missense_variant | 0.27 |
gid | 4407786 | c.417G>T | synonymous_variant | 0.15 |
gid | 4408372 | c.-170G>C | upstream_gene_variant | 0.2 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |