Run ID: ERR6336806
Sample name:
Date: 02-04-2023 02:04:10
Number of reads: 630834
Percentage reads mapped: 99.09
Strain: lineage1.2.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5148 | c.-92C>T | upstream_gene_variant | 0.12 |
gyrB | 5628 | p.Ala130Glu | missense_variant | 0.13 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7801 | p.Pro167His | missense_variant | 0.14 |
gyrA | 8444 | c.1144delC | frameshift_variant | 0.12 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9394 | p.Ser698Trp | missense_variant | 0.25 |
fgd1 | 491645 | p.Ser288Leu | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575538 | p.Asp64Gly | missense_variant | 0.14 |
mshA | 576671 | p.Arg442Trp | missense_variant | 0.25 |
ccsA | 620833 | p.Val315Ile | missense_variant | 0.22 |
rpoB | 759626 | c.-181C>T | upstream_gene_variant | 0.14 |
rpoB | 759972 | p.Glu56Lys | missense_variant | 0.22 |
rpoB | 760370 | c.564C>T | synonymous_variant | 0.22 |
rpoB | 760373 | c.567C>G | synonymous_variant | 0.22 |
rpoB | 760406 | c.600G>A | synonymous_variant | 0.17 |
rpoB | 760641 | p.Glu279Lys | missense_variant | 0.18 |
rpoB | 761467 | p.Leu554Pro | missense_variant | 0.13 |
rpoB | 762976 | p.Phe1057Tyr | missense_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 763942 | c.573C>A | synonymous_variant | 0.33 |
rpoC | 765874 | c.2505G>A | synonymous_variant | 0.13 |
rpoC | 766029 | p.Arg887Leu | missense_variant | 0.16 |
rpoC | 766032 | p.Glu888Ala | missense_variant | 0.18 |
rpoC | 766376 | p.Ile1003Val | missense_variant | 0.5 |
rpoC | 766739 | p.Val1124Met | missense_variant | 0.2 |
rpoC | 767050 | p.Gln1227His | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775925 | c.2556G>A | synonymous_variant | 0.17 |
mmpL5 | 776030 | c.2451G>C | synonymous_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776647 | p.Val612Ile | missense_variant | 0.12 |
mmpL5 | 777066 | p.Ile472Thr | missense_variant | 0.12 |
mmpL5 | 777368 | c.1113G>A | synonymous_variant | 0.12 |
mmpL5 | 777842 | c.639C>T | synonymous_variant | 0.17 |
mmpL5 | 779031 | c.-551G>A | upstream_gene_variant | 0.17 |
mmpR5 | 779247 | c.262dupG | frameshift_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781656 | p.Val33Leu | missense_variant | 0.1 |
fbiC | 1303045 | c.115C>T | synonymous_variant | 0.13 |
fbiC | 1303155 | c.225G>A | synonymous_variant | 0.14 |
fbiC | 1303498 | p.His190Asn | missense_variant | 0.13 |
fbiC | 1303661 | p.Val244Gly | missense_variant | 0.12 |
fbiC | 1303668 | c.738C>T | synonymous_variant | 0.13 |
fbiC | 1303812 | c.882C>T | synonymous_variant | 1.0 |
fbiC | 1304733 | p.Met601Ile | missense_variant | 0.15 |
fbiC | 1305196 | p.Ala756Thr | missense_variant | 0.2 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406641 | p.Thr234Ala | missense_variant | 0.12 |
Rv1258c | 1407095 | c.245delC | frameshift_variant | 0.18 |
embR | 1416856 | c.492G>A | synonymous_variant | 0.29 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417400 | c.-53C>G | upstream_gene_variant | 0.1 |
embR | 1417506 | c.-159T>C | upstream_gene_variant | 0.14 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472797 | n.952A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473916 | n.259C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474209 | n.552G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474893 | n.1236G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475021 | n.1364G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475880 | n.2223C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476621 | n.2964C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1674151 | p.Pro238Thr | missense_variant | 0.18 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
rpsA | 1833851 | p.Lys104Glu | missense_variant | 0.25 |
rpsA | 1834538 | p.Val333Met | missense_variant | 0.13 |
tlyA | 1917838 | c.-102G>A | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918520 | p.Pro194Arg | missense_variant | 0.29 |
ndh | 2102098 | c.945G>A | synonymous_variant | 0.13 |
ndh | 2102125 | c.918G>A | synonymous_variant | 0.14 |
katG | 2154351 | c.1761G>A | synonymous_variant | 0.12 |
katG | 2154556 | p.Arg519His | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154748 | p.Ile455Thr | missense_variant | 0.17 |
katG | 2154867 | c.1245G>A | synonymous_variant | 0.13 |
katG | 2156166 | c.-55T>G | upstream_gene_variant | 0.12 |
PPE35 | 2167693 | p.Gly974Ser | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.14 |
PPE35 | 2169614 | c.999C>T | synonymous_variant | 0.14 |
PPE35 | 2170662 | c.-50G>A | upstream_gene_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222499 | c.666G>C | synonymous_variant | 0.17 |
Rv1979c | 2223159 | c.5delT | frameshift_variant | 0.2 |
Rv1979c | 2223186 | c.-22C>A | upstream_gene_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288707 | p.Ser179Gly | missense_variant | 0.11 |
pncA | 2289660 | c.-419G>A | upstream_gene_variant | 0.12 |
pncA | 2289727 | c.-486G>A | upstream_gene_variant | 0.13 |
pncA | 2289837 | c.-596T>G | upstream_gene_variant | 0.22 |
pncA | 2289925 | c.-684T>A | upstream_gene_variant | 0.13 |
pncA | 2290169 | c.-928C>T | upstream_gene_variant | 0.15 |
kasA | 2517971 | c.-144G>C | upstream_gene_variant | 0.18 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518495 | c.381C>T | synonymous_variant | 0.17 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2714124 | c.1209A>C | stop_lost&splice_region_variant | 0.15 |
eis | 2714704 | p.Gly210Val | missense_variant | 0.13 |
ahpC | 2726041 | c.-152A>G | upstream_gene_variant | 0.11 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746368 | p.Ala411Ser | missense_variant | 0.15 |
folC | 2746649 | p.Ala317Val | missense_variant | 0.15 |
folC | 2746840 | c.759C>T | synonymous_variant | 0.12 |
Rv2752c | 3065045 | p.Phe383Leu | missense_variant | 0.12 |
Rv2752c | 3065094 | c.1098C>T | synonymous_variant | 0.17 |
Rv2752c | 3065454 | c.738G>A | synonymous_variant | 0.18 |
Rv2752c | 3065872 | p.Phe107Tyr | missense_variant | 0.22 |
Rv2752c | 3066996 | c.-805T>C | upstream_gene_variant | 0.13 |
thyX | 3067365 | p.His194Pro | missense_variant | 0.13 |
thyA | 3073786 | p.Lys229Arg | missense_variant | 0.12 |
thyA | 3074594 | c.-123C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087158 | c.339G>A | synonymous_variant | 0.12 |
ald | 3087632 | c.813G>A | synonymous_variant | 0.18 |
ald | 3087772 | p.Met318Thr | missense_variant | 0.14 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339613 | p.Ser166Thr | missense_variant | 0.25 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449218 | p.Val239Ile | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474656 | p.Asp217Val | missense_variant | 0.15 |
fprA | 3474659 | p.Leu218His | missense_variant | 0.15 |
fprA | 3475133 | p.Gln376Arg | missense_variant | 0.12 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612427 | c.690G>A | synonymous_variant | 0.14 |
Rv3236c | 3612905 | p.Leu71Ser | missense_variant | 0.14 |
Rv3236c | 3612915 | c.202T>C | synonymous_variant | 0.14 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640955 | p.Pro138Arg | missense_variant | 0.14 |
fbiA | 3641035 | p.Lys165* | stop_gained | 0.15 |
fbiA | 3641378 | p.Arg279Gln | missense_variant | 0.12 |
fbiB | 3641551 | p.His6Arg | missense_variant | 0.11 |
fbiB | 3641714 | c.180G>A | synonymous_variant | 0.25 |
fbiB | 3641974 | p.Val147Ala | missense_variant | 0.15 |
fbiB | 3642558 | p.Tyr342Asn | missense_variant | 0.14 |
fbiB | 3642752 | c.1218C>T | synonymous_variant | 0.13 |
alr | 3840554 | c.867G>A | synonymous_variant | 0.14 |
alr | 3841221 | p.Ala67Val | missense_variant | 0.12 |
rpoA | 3878239 | p.Asp90Val | missense_variant | 0.29 |
clpC1 | 4038955 | p.Glu584Gln | missense_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.25 |
clpC1 | 4040342 | c.363C>A | synonymous_variant | 0.18 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241285 | p.Pro475Ser | missense_variant | 0.14 |
embC | 4241512 | p.Met550Ile | missense_variant | 0.2 |
embC | 4241668 | c.1806G>A | synonymous_variant | 0.15 |
embC | 4241688 | c.1829delG | frameshift_variant | 0.15 |
embA | 4242247 | c.-986C>T | upstream_gene_variant | 0.15 |
embA | 4242439 | c.-794G>A | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243164 | c.-69G>A | upstream_gene_variant | 0.15 |
embA | 4243320 | p.Ile30Val | missense_variant | 0.14 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245463 | c.2235delC | frameshift_variant | 0.14 |
embB | 4245524 | c.-990G>C | upstream_gene_variant | 0.18 |
embA | 4245933 | p.Pro901Ala | missense_variant | 0.11 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246146 | p.Gly972Arg | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.42 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.38 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.36 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.38 |
embB | 4246984 | c.471C>T | synonymous_variant | 0.22 |
embB | 4247360 | p.Val283Met | missense_variant | 0.13 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248167 | p.Thr552Ala | missense_variant | 0.12 |
embB | 4249018 | c.2505T>C | synonymous_variant | 0.17 |
aftB | 4267637 | c.1200C>T | synonymous_variant | 0.13 |
aftB | 4268498 | c.339T>C | synonymous_variant | 0.18 |
aftB | 4269252 | c.-416C>T | upstream_gene_variant | 0.14 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4327394 | p.Cys27Ser | missense_variant | 0.14 |
ethA | 4327398 | p.Arg26Gly | missense_variant | 0.14 |
ethA | 4327719 | c.-246C>A | upstream_gene_variant | 0.17 |
ethA | 4328458 | c.-985C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408170 | p.Ile11Met | missense_variant | 1.0 |