Run ID: ERR6336803
Sample name:
Date: 02-04-2023 02:03:54
Number of reads: 443568
Percentage reads mapped: 99.33
Strain: lineage1.2.1.2.1
Drug-resistance: Other
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 |
---|---|---|---|---|---|
embB | 4249583 | p.Asp1024Asn | missense_variant | 0.5 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5468 | p.Val77Ile | missense_variant | 0.12 |
gyrB | 5923 | c.684G>A | synonymous_variant | 0.2 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6495 | p.Ala419Glu | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.15 |
gyrA | 8091 | p.Arg264Cys | missense_variant | 0.15 |
gyrA | 8113 | p.Ile271Thr | missense_variant | 0.18 |
gyrA | 8407 | p.Gln369Arg | missense_variant | 0.25 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8554 | p.Arg418Gln | missense_variant | 0.17 |
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 | 9753 | p.Asn818Tyr | missense_variant | 0.17 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 0.43 |
fgd1 | 491395 | p.Glu205Lys | missense_variant | 0.17 |
fgd1 | 491411 | p.Ala210Val | missense_variant | 0.14 |
fgd1 | 491738 | p.Arg319Gln | missense_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.25 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.33 |
mshA | 576498 | p.Gly384Val | missense_variant | 0.4 |
ccsA | 620314 | c.424C>T | synonymous_variant | 0.13 |
ccsA | 620320 | p.Pro144Ser | missense_variant | 0.12 |
ccsA | 620503 | p.Glu205Lys | missense_variant | 0.33 |
ccsA | 620811 | c.921G>A | synonymous_variant | 0.13 |
rpoB | 759836 | c.31delG | frameshift_variant | 0.22 |
rpoB | 760544 | c.738C>T | synonymous_variant | 0.33 |
rpoB | 760742 | c.936G>A | synonymous_variant | 0.33 |
rpoB | 760756 | p.His317Arg | missense_variant | 0.2 |
rpoB | 760901 | c.1095C>T | synonymous_variant | 0.25 |
rpoB | 762322 | p.Gly839Asp | missense_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763353 | c.-17A>T | upstream_gene_variant | 0.13 |
rpoC | 763459 | c.90G>A | synonymous_variant | 0.25 |
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 | 764138 | p.Gly257Arg | missense_variant | 0.22 |
rpoC | 764938 | c.1569G>A | synonymous_variant | 0.2 |
rpoC | 765767 | p.Ile800Val | missense_variant | 0.13 |
rpoC | 765903 | p.Thr845Ile | missense_variant | 0.33 |
rpoC | 767217 | p.Tyr1283Cys | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776683 | c.1798C>T | synonymous_variant | 0.14 |
mmpL5 | 776791 | p.Val564Ile | missense_variant | 0.33 |
mmpL5 | 776821 | p.Val554Ile | missense_variant | 0.33 |
mmpL5 | 776876 | c.1605G>A | synonymous_variant | 0.33 |
mmpL5 | 778212 | p.Ala90Glu | missense_variant | 0.2 |
mmpL5 | 778422 | p.Ala20Val | missense_variant | 0.15 |
mmpL5 | 778426 | p.Ala19Thr | missense_variant | 0.15 |
mmpS5 | 778755 | p.Phe51Leu | missense_variant | 0.15 |
mmpS5 | 779645 | c.-740C>T | upstream_gene_variant | 0.22 |
rpsL | 781384 | c.-176G>A | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303812 | c.882C>T | synonymous_variant | 1.0 |
fbiC | 1304322 | c.1392C>T | synonymous_variant | 0.12 |
fbiC | 1304575 | p.Asn549Asp | missense_variant | 0.14 |
fbiC | 1304731 | p.Met601Val | missense_variant | 0.14 |
fbiC | 1304736 | c.1806G>A | synonymous_variant | 0.14 |
fbiC | 1304873 | p.Ser648Asn | missense_variant | 0.22 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406649 | p.Ile231Asn | missense_variant | 0.12 |
Rv1258c | 1407058 | p.Gly95Arg | missense_variant | 0.11 |
Rv1258c | 1407421 | c.-81A>T | upstream_gene_variant | 0.29 |
embR | 1416316 | c.1032C>A | synonymous_variant | 0.15 |
embR | 1416848 | p.Val167Glu | missense_variant | 0.22 |
embR | 1416916 | c.432A>G | synonymous_variant | 0.13 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460861 | c.-184C>T | 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 | 1471759 | n.-87A>G | upstream_gene_variant | 0.14 |
rrs | 1471768 | n.-78T>C | upstream_gene_variant | 0.12 |
rrs | 1472717 | n.872C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473516 | n.-142G>T | upstream_gene_variant | 0.25 |
rrl | 1474425 | n.768A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474428 | n.771C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475226 | n.1569C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475250 | n.1593C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475478 | n.1821G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475711 | n.2054T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475744 | n.2087A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476274 | n.2617G>A | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673251 | c.-189T>A | upstream_gene_variant | 0.18 |
inhA | 1673718 | c.-484G>T | upstream_gene_variant | 0.2 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
rpsA | 1834060 | c.519C>T | synonymous_variant | 0.15 |
rpsA | 1834330 | c.789C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918215 | c.276G>A | synonymous_variant | 0.25 |
tlyA | 1918367 | p.Ala143Val | missense_variant | 0.25 |
tlyA | 1918670 | p.Arg244His | missense_variant | 0.18 |
ndh | 2102221 | c.821delA | frameshift_variant | 0.2 |
ndh | 2102659 | c.384C>T | synonymous_variant | 0.22 |
katG | 2154056 | p.Lys686Glu | missense_variant | 0.15 |
katG | 2154271 | p.Ala614Val | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155107 | c.1005C>T | synonymous_variant | 0.12 |
katG | 2155785 | c.327T>G | synonymous_variant | 0.4 |
katG | 2156215 | c.-104G>A | upstream_gene_variant | 0.15 |
katG | 2156360 | c.-249T>C | upstream_gene_variant | 0.15 |
katG | 2156364 | c.-253T>G | upstream_gene_variant | 0.17 |
katG | 2156501 | c.-390C>T | upstream_gene_variant | 0.2 |
PPE35 | 2167693 | p.Gly974Ser | missense_variant | 1.0 |
PPE35 | 2167836 | p.Gly926Glu | missense_variant | 0.18 |
PPE35 | 2167898 | c.2715G>A | synonymous_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168079 | p.Thr845Ile | missense_variant | 0.12 |
PPE35 | 2169003 | p.Leu537Ser | missense_variant | 0.29 |
PPE35 | 2169466 | p.Asn383Asp | missense_variant | 0.5 |
PPE35 | 2170223 | c.390T>C | synonymous_variant | 0.38 |
PPE35 | 2170678 | c.-66C>T | upstream_gene_variant | 0.14 |
Rv1979c | 2221820 | p.Ile449Phe | missense_variant | 0.18 |
Rv1979c | 2222169 | c.996C>T | synonymous_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222336 | p.Leu277Phe | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288905 | p.Gly113Ser | missense_variant | 0.14 |
pncA | 2289102 | p.Thr47Ile | missense_variant | 0.15 |
pncA | 2289541 | c.-300G>A | upstream_gene_variant | 0.12 |
pncA | 2289897 | c.-656G>T | upstream_gene_variant | 0.13 |
pncA | 2289987 | c.-746C>T | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518322 | p.Ser70Gly | missense_variant | 0.17 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519076 | p.Ala321Val | missense_variant | 0.22 |
eis | 2714207 | p.Arg376Cys | missense_variant | 0.2 |
eis | 2714501 | c.832C>T | synonymous_variant | 0.2 |
eis | 2714528 | p.Thr269Ser | missense_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726515 | c.326delC | frameshift_variant | 0.22 |
ahpC | 2726670 | p.Glu160Gln | missense_variant | 0.18 |
folC | 2746147 | c.1452T>C | synonymous_variant | 0.14 |
pepQ | 2859914 | p.Glu169Lys | missense_variant | 0.22 |
Rv2752c | 3065220 | c.972C>T | synonymous_variant | 0.14 |
Rv2752c | 3065398 | p.Ser265Leu | missense_variant | 0.14 |
Rv2752c | 3065646 | c.546C>T | synonymous_variant | 0.29 |
Rv2752c | 3066035 | p.Asp53Asn | missense_variant | 0.2 |
thyX | 3067661 | c.285C>T | synonymous_variant | 0.14 |
thyA | 3074367 | c.105C>G | synonymous_variant | 0.2 |
thyA | 3074567 | c.-96C>T | upstream_gene_variant | 0.13 |
thyA | 3074594 | c.-123C>T | upstream_gene_variant | 1.0 |
ald | 3086769 | c.-50delT | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087313 | p.Gly165Val | missense_variant | 0.15 |
ald | 3087615 | p.Asp266Asn | missense_variant | 0.17 |
fbiD | 3339155 | p.Ile13Thr | missense_variant | 0.2 |
fbiD | 3339222 | c.105C>T | synonymous_variant | 0.17 |
fbiD | 3339264 | c.147C>T | synonymous_variant | 0.18 |
fbiD | 3339327 | c.210T>A | synonymous_variant | 0.14 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
Rv3083 | 3448454 | c.-50C>T | upstream_gene_variant | 0.15 |
Rv3083 | 3448707 | c.204G>A | synonymous_variant | 0.17 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448758 | c.255C>T | synonymous_variant | 0.17 |
Rv3083 | 3449134 | p.Gln211* | stop_gained | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474646 | p.Glu214Lys | missense_variant | 0.14 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612338 | p.Arg260His | missense_variant | 0.12 |
Rv3236c | 3612816 | p.Ala101Thr | missense_variant | 0.22 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiB | 3642180 | p.Val216Met | missense_variant | 0.18 |
fbiB | 3642513 | p.Pro327Ala | missense_variant | 0.15 |
fbiB | 3642525 | p.Ile331Val | missense_variant | 0.2 |
alr | 3840227 | c.1194C>T | synonymous_variant | 0.15 |
alr | 3840323 | c.1098C>T | synonymous_variant | 0.2 |
alr | 3840630 | p.Pro264Leu | missense_variant | 0.29 |
ddn | 3987044 | c.201G>C | synonymous_variant | 0.22 |
ddn | 3987050 | c.207C>T | synonymous_variant | 0.25 |
clpC1 | 4040014 | p.Gln231* | stop_gained | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239847 | c.-16C>T | upstream_gene_variant | 0.25 |
embC | 4240038 | p.Leu59Ser | missense_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240932 | p.Trp357* | stop_gained | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242209 | p.Glu783Lys | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243034 | p.Gly1058Ser | missense_variant | 0.22 |
embA | 4243304 | c.73delC | frameshift_variant | 0.2 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244019 | p.Leu263Val | missense_variant | 0.4 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244995 | p.Thr588Ile | missense_variant | 0.25 |
embA | 4245753 | p.Gly841Ser | missense_variant | 0.17 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.6 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.43 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.43 |
embB | 4247123 | p.Ala204Thr | missense_variant | 0.5 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247679 | p.Met389Thr | missense_variant | 0.11 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.38 |
embB | 4248913 | p.Glu800Asp | missense_variant | 0.17 |
embB | 4248979 | c.2466G>A | synonymous_variant | 0.12 |
embB | 4249026 | p.Asp838Gly | missense_variant | 0.13 |
aftB | 4267392 | p.Pro482Leu | missense_variant | 0.13 |
aftB | 4267589 | p.Gln416His | missense_variant | 0.2 |
aftB | 4268064 | p.Ser258Trp | missense_variant | 0.14 |
aftB | 4268826 | c.10dupG | frameshift_variant | 0.13 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269436 | c.397delG | frameshift_variant | 0.22 |
ubiA | 4269445 | p.Val130Gly | missense_variant | 0.22 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269773 | p.Ile21Val | missense_variant | 0.11 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4326379 | c.1095G>A | synonymous_variant | 0.14 |
ethA | 4326605 | p.Asp290Gly | missense_variant | 0.18 |
ethA | 4327359 | p.Glu39Lys | missense_variant | 0.29 |
ethA | 4328187 | c.-714G>A | upstream_gene_variant | 0.25 |
ethA | 4328193 | c.-720G>A | upstream_gene_variant | 0.33 |
whiB6 | 4338214 | p.Gly103Asp | missense_variant | 0.25 |
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 | 4407626 | p.Ala193Thr | missense_variant | 0.14 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408004 | p.Asp67Tyr | missense_variant | 0.17 |
gid | 4408044 | c.159C>T | synonymous_variant | 0.14 |
gid | 4408170 | p.Ile11Met | missense_variant | 1.0 |