Run ID: ERR4596937
Sample name:
Date: 01-04-2023 06:30:05
Number of reads: 681933
Percentage reads mapped: 16.11
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 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.25 |
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 | 764623 | c.1254C>G | synonymous_variant | 0.12 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.12 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.12 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.15 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 0.16 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.15 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.14 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.14 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.14 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 767317 | c.3948C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776445 | p.Ala679Val | missense_variant | 0.12 |
mmpL5 | 776802 | p.Met560Lys | missense_variant | 0.12 |
mmpL5 | 777436 | p.Ala349Thr | missense_variant | 0.15 |
mmpL5 | 778155 | c.325delT | frameshift_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406698 | p.Gly215Trp | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472972 | n.1127T>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472974 | n.1130_1133delTGGT | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473054 | n.1209C>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473070 | n.1225G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473071 | n.1226C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673283 | c.-157A>C | upstream_gene_variant | 1.0 |
inhA | 1674933 | c.732G>T | synonymous_variant | 0.17 |
tlyA | 1917777 | c.-163A>G | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918106 | p.Thr56Ile | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155557 | c.555C>T | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.94 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2170378 | p.Ala79Thr | missense_variant | 1.0 |
Rv1979c | 2221783 | p.Ala461Glu | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519005 | c.891G>A | synonymous_variant | 0.12 |
eis | 2714199 | p.Lys378Asn | missense_variant | 1.0 |
eis | 2714874 | c.459A>C | synonymous_variant | 0.11 |
ahpC | 2725931 | c.-262_-261insG | upstream_gene_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 1.0 |
pepQ | 2859968 | p.Asp151Asn | missense_variant | 0.13 |
pepQ | 2860504 | c.-86A>T | upstream_gene_variant | 0.14 |
ribD | 2986711 | c.-128G>A | upstream_gene_variant | 0.14 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086963 | c.144G>A | synonymous_variant | 0.17 |
ald | 3087033 | p.Leu72Phe | missense_variant | 0.14 |
ald | 3087872 | c.1053G>A | synonymous_variant | 0.14 |
Rv3083 | 3448442 | c.-62A>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448649 | p.Arg49His | missense_variant | 0.13 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449567 | p.Gly355Val | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474176 | c.174dupC | frameshift_variant | 0.17 |
fprA | 3474502 | p.Leu166Met | missense_variant | 0.13 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612297 | p.Phe274Leu | missense_variant | 0.11 |
Rv3236c | 3613012 | c.105G>A | synonymous_variant | 1.0 |
Rv3236c | 3613116 | p.Val1Leu | missense_variant | 0.17 |
fbiA | 3640636 | p.Ser32Thr | missense_variant | 0.18 |
fbiB | 3640758 | c.-777G>T | upstream_gene_variant | 0.18 |
alr | 3840262 | p.His387Tyr | missense_variant | 1.0 |
clpC1 | 4038558 | p.Ile716Thr | missense_variant | 0.25 |
clpC1 | 4039330 | p.Ala459Thr | missense_variant | 0.14 |
clpC1 | 4039935 | p.Ala257Val | missense_variant | 0.17 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240186 | c.324G>A | synonymous_variant | 0.2 |
embC | 4240569 | p.Leu236Arg | missense_variant | 0.12 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240794 | p.Ala311Asp | missense_variant | 0.18 |
embC | 4241011 | c.1149C>T | synonymous_variant | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242073 | c.2211C>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242898 | c.-335G>A | upstream_gene_variant | 0.13 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244799 | p.Val523Leu | missense_variant | 0.18 |
embA | 4244982 | c.1750T>C | synonymous_variant | 0.12 |
embA | 4245166 | p.Pro645Gln | missense_variant | 1.0 |
embA | 4245907 | p.Leu892Pro | missense_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246095 | p.Ala955Thr | missense_variant | 0.15 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.29 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267886 | c.951C>T | synonymous_variant | 0.18 |
ubiA | 4269025 | p.Leu270Pro | missense_variant | 0.15 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269876 | c.-43C>T | upstream_gene_variant | 0.2 |
ubiA | 4269890 | c.-57G>A | upstream_gene_variant | 0.15 |
whiB6 | 4338386 | p.Asp46Asn | missense_variant | 0.12 |
whiB6 | 4338503 | p.Ala7Thr | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338617 | c.-96C>T | upstream_gene_variant | 0.14 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |