Run ID: ERR4818637
Sample name:
Date: 01-04-2023 15:40:09
Number of reads: 495018
Percentage reads mapped: 90.01
Strain: lineage4.8
Drug-resistance: Other
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 1.0 | streptomycin |
gid | 4407952 | p.Pro84Leu | missense_variant | 0.18 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5205 | c.-35G>A | upstream_gene_variant | 0.25 |
gyrB | 5234 | c.-6C>T | upstream_gene_variant | 0.2 |
gyrB | 5642 | p.Leu135Ile | missense_variant | 0.25 |
gyrB | 5863 | c.624G>A | synonymous_variant | 0.22 |
gyrB | 6227 | p.Lys330* | stop_gained | 0.25 |
gyrB | 6432 | p.Ala398Asp | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7434 | p.Arg45Cys | missense_variant | 0.18 |
gyrA | 7847 | c.546G>T | synonymous_variant | 0.2 |
fgd1 | 490670 | c.-113G>T | upstream_gene_variant | 0.4 |
fgd1 | 490878 | p.Met32Ile | missense_variant | 0.15 |
fgd1 | 491030 | p.Pro83His | missense_variant | 0.33 |
fgd1 | 491746 | p.Glu322* | stop_gained | 0.17 |
mshA | 575983 | c.636G>A | synonymous_variant | 0.29 |
mshA | 576427 | c.1080G>A | synonymous_variant | 0.14 |
mshA | 576576 | p.Ala410Val | missense_variant | 0.12 |
ccsA | 620176 | p.Val96Leu | missense_variant | 0.2 |
rpoB | 759682 | c.-125G>T | upstream_gene_variant | 0.17 |
rpoB | 760565 | c.759A>T | synonymous_variant | 0.14 |
rpoB | 760657 | p.Glu284Gly | missense_variant | 0.2 |
rpoB | 760681 | p.Asn292Ser | missense_variant | 1.0 |
rpoB | 761012 | p.Asp402Glu | missense_variant | 0.14 |
rpoB | 761540 | c.1734C>A | synonymous_variant | 0.5 |
rpoB | 761929 | p.Ala708Val | missense_variant | 0.22 |
rpoB | 762021 | p.Asp739Tyr | missense_variant | 0.18 |
rpoB | 762681 | p.Glu959* | stop_gained | 0.18 |
rpoB | 762748 | p.Gly981Ala | missense_variant | 0.17 |
rpoC | 763977 | p.Arg203His | missense_variant | 0.2 |
rpoC | 764671 | c.1302G>A | synonymous_variant | 0.22 |
rpoC | 764854 | c.1485G>T | synonymous_variant | 0.17 |
rpoC | 765374 | p.Gly669Cys | missense_variant | 0.18 |
rpoC | 765403 | c.2034G>A | synonymous_variant | 0.2 |
rpoC | 765448 | p.Gln693His | missense_variant | 0.33 |
rpoC | 766053 | p.Arg895His | missense_variant | 0.17 |
rpoC | 766616 | c.3247C>A | synonymous_variant | 0.15 |
mmpL5 | 775634 | c.2847G>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776247 | p.Ala745Asp | missense_variant | 0.2 |
mmpL5 | 776378 | p.Phe701Leu | missense_variant | 0.33 |
mmpL5 | 776923 | p.Ala520Ser | missense_variant | 0.67 |
mmpL5 | 777182 | c.1299C>A | synonymous_variant | 0.29 |
mmpL5 | 777521 | c.960C>G | synonymous_variant | 0.22 |
mmpL5 | 777655 | p.Asp276Tyr | missense_variant | 0.22 |
mmpL5 | 777948 | p.Pro178Leu | missense_variant | 0.2 |
mmpS5 | 779682 | c.-777G>T | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800789 | c.-20G>A | upstream_gene_variant | 0.15 |
rplC | 801022 | p.Ala72Thr | missense_variant | 0.29 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.15 |
fbiC | 1304927 | p.Gly666Val | missense_variant | 0.2 |
fbiC | 1305086 | p.Trp719Leu | missense_variant | 0.17 |
fbiC | 1305193 | p.Gly755Cys | missense_variant | 0.17 |
Rv1258c | 1407350 | c.-10C>T | upstream_gene_variant | 0.13 |
Rv1258c | 1407446 | c.-106G>A | upstream_gene_variant | 0.17 |
embR | 1416348 | p.Asp334Tyr | missense_variant | 0.22 |
embR | 1416645 | p.Leu235Met | missense_variant | 0.22 |
embR | 1417050 | p.Gly100Ser | missense_variant | 0.25 |
embR | 1417212 | p.Arg46Cys | missense_variant | 0.15 |
embR | 1417242 | p.Arg36Trp | missense_variant | 0.15 |
embR | 1417496 | c.-149C>T | upstream_gene_variant | 0.2 |
atpE | 1460916 | c.-129G>A | upstream_gene_variant | 0.33 |
rrs | 1472094 | n.249T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472100 | n.255T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473364 | n.1519G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475154 | n.1497C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673536 | p.Gln33Lys | missense_variant | 0.67 |
inhA | 1674993 | c.792G>A | synonymous_variant | 1.0 |
rpsA | 1833354 | c.-188G>A | upstream_gene_variant | 0.25 |
rpsA | 1834595 | p.Asp352Tyr | missense_variant | 0.2 |
tlyA | 1918474 | p.Pro179Ser | missense_variant | 0.17 |
tlyA | 1918602 | c.663C>T | synonymous_variant | 0.22 |
ndh | 2102218 | c.825C>T | synonymous_variant | 0.22 |
ndh | 2103020 | p.Thr8Ile | missense_variant | 0.29 |
ndh | 2103209 | c.-167C>T | upstream_gene_variant | 0.17 |
katG | 2155740 | c.372C>A | synonymous_variant | 0.5 |
katG | 2156236 | c.-125C>A | upstream_gene_variant | 0.33 |
katG | 2156483 | c.-372C>A | upstream_gene_variant | 0.18 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169393 | p.Ala407Asp | missense_variant | 0.18 |
PPE35 | 2169458 | c.1155C>A | synonymous_variant | 0.4 |
PPE35 | 2169908 | p.Asn235Lys | missense_variant | 0.5 |
PPE35 | 2170463 | c.150C>A | synonymous_variant | 0.2 |
Rv1979c | 2221893 | c.1272C>A | synonymous_variant | 0.25 |
Rv1979c | 2222132 | p.Gln345Lys | missense_variant | 0.2 |
Rv1979c | 2222502 | p.Met221Ile | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288825 | c.417G>T | synonymous_variant | 0.2 |
kasA | 2518970 | p.Arg286Cys | missense_variant | 0.33 |
eis | 2714944 | p.Gly130Asp | missense_variant | 0.2 |
eis | 2714969 | p.Glu122Lys | missense_variant | 0.33 |
eis | 2715492 | c.-160G>T | upstream_gene_variant | 0.29 |
eis | 2715528 | c.-196G>T | upstream_gene_variant | 0.5 |
ahpC | 2725963 | c.-230G>T | upstream_gene_variant | 0.22 |
ahpC | 2726192 | c.-1C>A | upstream_gene_variant | 0.25 |
folC | 2746159 | c.1440C>A | synonymous_variant | 0.22 |
folC | 2746287 | p.Asp438His | missense_variant | 0.33 |
pepQ | 2860217 | p.Ala68Ser | missense_variant | 0.29 |
pepQ | 2860297 | p.Gly41Val | missense_variant | 0.33 |
pepQ | 2860365 | c.54G>A | synonymous_variant | 0.18 |
ribD | 2986878 | p.Leu14Ile | missense_variant | 0.13 |
ribD | 2987549 | c.711G>A | synonymous_variant | 0.14 |
ribD | 2987556 | p.Cys240Ser | missense_variant | 0.15 |
Rv2752c | 3064581 | c.1611C>A | synonymous_variant | 0.25 |
Rv2752c | 3064753 | p.Arg480Lys | missense_variant | 0.17 |
Rv2752c | 3064820 | p.Gly458Ser | missense_variant | 0.22 |
Rv2752c | 3065306 | p.Ala296Thr | missense_variant | 0.12 |
Rv2752c | 3065322 | c.870C>T | synonymous_variant | 0.14 |
Rv2752c | 3066360 | c.-170delG | upstream_gene_variant | 0.17 |
thyX | 3067436 | c.510C>T | synonymous_variant | 0.15 |
thyA | 3074403 | c.69C>A | synonymous_variant | 0.29 |
ald | 3087069 | p.Arg84Ser | missense_variant | 0.2 |
ald | 3087152 | c.333C>A | synonymous_variant | 1.0 |
ald | 3087203 | c.384C>A | synonymous_variant | 0.29 |
ald | 3087243 | p.Ala142Ser | missense_variant | 0.29 |
ald | 3087287 | c.468C>T | synonymous_variant | 0.25 |
ald | 3087460 | p.Arg214Gln | missense_variant | 0.33 |
fbiD | 3339008 | c.-110A>G | upstream_gene_variant | 0.13 |
fbiD | 3339506 | p.Ser130Leu | missense_variant | 0.25 |
Rv3083 | 3448350 | c.-154G>A | upstream_gene_variant | 0.12 |
Rv3083 | 3448361 | c.-143G>A | upstream_gene_variant | 0.18 |
fprA | 3473999 | c.-8G>T | upstream_gene_variant | 0.2 |
fprA | 3474511 | p.Asp169Tyr | missense_variant | 0.2 |
fprA | 3474711 | p.Asp235Glu | missense_variant | 0.29 |
fprA | 3474834 | c.828C>T | synonymous_variant | 0.15 |
fprA | 3474885 | c.879G>A | synonymous_variant | 0.22 |
whiB7 | 3568431 | c.249C>T | synonymous_variant | 0.13 |
whiB7 | 3568822 | c.-143C>G | upstream_gene_variant | 0.17 |
Rv3236c | 3612351 | p.Ala256Thr | missense_variant | 0.15 |
Rv3236c | 3612877 | c.240C>T | synonymous_variant | 0.4 |
fbiA | 3640714 | p.Val58Phe | missense_variant | 0.12 |
fbiA | 3641503 | p.Arg321Cys | missense_variant | 0.2 |
fbiB | 3641608 | p.Pro25His | missense_variant | 0.2 |
alr | 3840409 | p.Val338Leu | missense_variant | 0.17 |
alr | 3840459 | p.Ser321Leu | missense_variant | 0.29 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.15 |
alr | 3841059 | p.Gly121Glu | missense_variant | 0.13 |
alr | 3841084 | p.Leu113Met | missense_variant | 0.12 |
alr | 3841185 | c.235delC | frameshift_variant | 1.0 |
rpoA | 3877539 | c.969C>T | synonymous_variant | 0.15 |
rpoA | 3877959 | c.549C>T | synonymous_variant | 0.33 |
ddn | 3986753 | c.-91G>T | upstream_gene_variant | 0.22 |
ddn | 3986843 | c.-1C>A | upstream_gene_variant | 0.33 |
ddn | 3987173 | c.330C>T | synonymous_variant | 0.17 |
clpC1 | 4038383 | c.2322G>A | synonymous_variant | 0.13 |
clpC1 | 4038771 | p.Gly645Val | missense_variant | 0.33 |
clpC1 | 4039671 | p.Val345Glu | missense_variant | 0.15 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
clpC1 | 4040896 | c.-192C>T | upstream_gene_variant | 0.22 |
embC | 4240320 | p.Gln153Arg | missense_variant | 0.22 |
embC | 4241137 | c.1275G>T | synonymous_variant | 0.33 |
embC | 4241197 | c.1335G>T | synonymous_variant | 0.22 |
embC | 4242216 | p.Phe785Ser | missense_variant | 0.4 |
embC | 4242491 | p.Arg877Trp | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242675 | p.Ser938Asn | missense_variant | 0.33 |
embA | 4242724 | c.-509G>A | upstream_gene_variant | 0.25 |
embC | 4242762 | p.Arg967Leu | missense_variant | 0.14 |
embA | 4242997 | c.-236G>A | upstream_gene_variant | 0.4 |
embA | 4243846 | p.Ala205Asp | missense_variant | 0.18 |
embA | 4244195 | c.963C>A | synonymous_variant | 0.14 |
embA | 4245098 | c.1866C>T | synonymous_variant | 0.15 |
embA | 4245314 | c.2082G>A | synonymous_variant | 0.25 |
embA | 4246265 | p.His1011Gln | missense_variant | 0.13 |
embB | 4246821 | p.Pro103His | missense_variant | 0.18 |
embB | 4246979 | p.Gly156Ser | missense_variant | 0.17 |
embB | 4247606 | c.1093C>T | synonymous_variant | 0.18 |
embB | 4247689 | c.1176G>A | synonymous_variant | 0.13 |
embB | 4248298 | p.His595Gln | missense_variant | 0.15 |
embB | 4249077 | p.Gln855Leu | missense_variant | 0.14 |
embB | 4249151 | p.Ala880Ser | missense_variant | 0.15 |
aftB | 4266961 | p.Arg626Trp | missense_variant | 0.14 |
aftB | 4267061 | p.Leu592Phe | missense_variant | 0.14 |
aftB | 4267128 | p.Ala570Glu | missense_variant | 0.4 |
aftB | 4267284 | p.Thr518Ile | missense_variant | 0.14 |
aftB | 4268332 | p.Gln169Lys | missense_variant | 0.14 |
aftB | 4268350 | p.Arg163Trp | missense_variant | 0.14 |
ubiA | 4269309 | p.Trp175Cys | missense_variant | 1.0 |
ubiA | 4269490 | p.Ala115Asp | missense_variant | 0.33 |
aftB | 4269621 | c.-785C>A | upstream_gene_variant | 0.17 |
ubiA | 4269959 | c.-126C>A | upstream_gene_variant | 0.29 |
ethA | 4326762 | p.Val238Ile | missense_variant | 0.18 |
ethA | 4328184 | c.-711G>A | upstream_gene_variant | 0.22 |
ethA | 4328215 | c.-742C>A | upstream_gene_variant | 0.15 |
ethA | 4328282 | c.-809C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338383 | p.Asp47Tyr | missense_variant | 0.2 |
whiB6 | 4338399 | p.Trp41Cys | missense_variant | 0.22 |
whiB6 | 4338435 | c.87C>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338646 | c.-125A>T | upstream_gene_variant | 0.22 |
gid | 4407914 | p.Arg97Cys | missense_variant | 0.18 |
gid | 4408260 | c.-58A>G | upstream_gene_variant | 0.2 |