Run ID: ERR6336766
Sample name:
Date: 02-04-2023 02:02:34
Number of reads: 954853
Percentage reads mapped: 98.93
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 |
---|---|---|---|---|---|
tlyA | 1918487 | p.Pro183Leu | missense_variant | 0.15 | capreomycin |
pncA | 2289036 | p.Pro69Leu | missense_variant | 0.13 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5234 | c.-6C>T | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7376 | c.75G>A | synonymous_variant | 0.13 |
gyrA | 7418 | c.117C>T | synonymous_variant | 0.29 |
gyrA | 7423 | p.Leu41Gln | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7720 | p.Glu140Gly | missense_variant | 0.12 |
gyrA | 7728 | p.Arg143Gly | missense_variant | 0.12 |
gyrA | 7781 | c.480G>C | synonymous_variant | 0.22 |
gyrA | 7795 | p.Val165Ala | missense_variant | 0.22 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8833 | p.Ile511Thr | missense_variant | 0.11 |
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 |
fgd1 | 490864 | p.Glu28Lys | missense_variant | 0.2 |
fgd1 | 491082 | c.300T>G | synonymous_variant | 0.11 |
fgd1 | 491309 | p.Ala176Gly | missense_variant | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 576099 | p.Asp251Gly | missense_variant | 0.67 |
ccsA | 619929 | c.39C>T | synonymous_variant | 0.12 |
ccsA | 620853 | c.963G>C | synonymous_variant | 0.14 |
rpoB | 760937 | c.1131G>A | synonymous_variant | 0.17 |
rpoB | 761164 | p.Gly453Glu | missense_variant | 0.33 |
rpoB | 761502 | p.Pro566Ser | missense_variant | 0.22 |
rpoB | 761701 | p.Ala632Val | missense_variant | 0.29 |
rpoB | 761710 | p.Val635Asp | missense_variant | 0.38 |
rpoB | 761713 | p.Val636Asp | missense_variant | 0.44 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.25 |
rpoB | 762285 | p.Arg827Cys | missense_variant | 0.22 |
rpoC | 762701 | c.-669T>C | upstream_gene_variant | 0.12 |
rpoB | 762954 | p.Pro1050Ser | missense_variant | 0.5 |
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 | 763901 | p.Glu178Lys | missense_variant | 0.25 |
rpoC | 763981 | c.612G>A | synonymous_variant | 0.67 |
rpoC | 764383 | c.1014C>T | synonymous_variant | 0.2 |
rpoC | 764514 | p.Phe382Ser | missense_variant | 0.12 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.25 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.13 |
rpoC | 766258 | c.2889T>A | synonymous_variant | 0.18 |
rpoC | 766444 | c.3075C>T | synonymous_variant | 0.2 |
rpoC | 766468 | p.Glu1033Asp | missense_variant | 0.22 |
rpoC | 766533 | p.Leu1055His | missense_variant | 0.25 |
rpoC | 766604 | p.Lys1079Glu | missense_variant | 0.14 |
rpoC | 766614 | c.3247_3248delCG | frameshift_variant | 0.14 |
rpoC | 766692 | p.Gly1108Asp | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776233 | p.Pro750Ala | missense_variant | 0.13 |
mmpL5 | 776272 | p.Lys737Glu | missense_variant | 0.2 |
mmpL5 | 777170 | p.His437Arg | missense_variant | 0.15 |
mmpL5 | 777514 | p.Cys323Arg | missense_variant | 0.11 |
mmpL5 | 777554 | p.Val309Gly | missense_variant | 0.17 |
mmpL5 | 778161 | p.Ala107Gly | missense_variant | 0.14 |
mmpR5 | 778415 | c.-575C>T | upstream_gene_variant | 0.14 |
mmpL5 | 778452 | p.Thr10Arg | missense_variant | 0.2 |
mmpS5 | 778491 | p.Val139Met | missense_variant | 0.13 |
mmpL5 | 779271 | c.-791C>T | upstream_gene_variant | 0.22 |
mmpR5 | 779276 | p.Arg96Gln | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781688 | c.129G>A | synonymous_variant | 0.13 |
fbiC | 1303450 | p.Val174Met | missense_variant | 0.5 |
fbiC | 1303564 | p.Gly212Ser | missense_variant | 0.13 |
fbiC | 1304288 | p.Ile453Asn | missense_variant | 0.17 |
fbiC | 1304639 | p.Arg570Gln | missense_variant | 0.13 |
fbiC | 1304668 | p.Ser580Pro | missense_variant | 0.25 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406755 | p.Ala196Thr | missense_variant | 0.67 |
Rv1258c | 1407191 | c.150G>A | synonymous_variant | 0.17 |
embR | 1416631 | c.717C>T | synonymous_variant | 0.13 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474425 | n.768A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474428 | n.771C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673913 | c.-289C>G | upstream_gene_variant | 0.15 |
fabG1 | 1674013 | c.575delG | frameshift_variant | 0.18 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674660 | c.459G>A | synonymous_variant | 0.14 |
rpsA | 1833864 | p.Gln108Arg | missense_variant | 0.13 |
rpsA | 1834871 | p.Gly444Ser | missense_variant | 0.67 |
tlyA | 1917857 | c.-83C>T | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918121 | p.Ala61Val | missense_variant | 0.2 |
ndh | 2101665 | p.Lys460Glu | missense_variant | 0.22 |
ndh | 2102397 | p.Ala216Thr | missense_variant | 0.22 |
ndh | 2102469 | c.574C>T | synonymous_variant | 0.14 |
ndh | 2102499 | p.Gly182Ser | missense_variant | 0.14 |
ndh | 2103175 | c.-133G>A | upstream_gene_variant | 0.18 |
katG | 2154431 | p.His561Tyr | missense_variant | 0.18 |
katG | 2154449 | p.Ala555Thr | missense_variant | 0.15 |
katG | 2154612 | c.1500G>A | synonymous_variant | 0.18 |
katG | 2154620 | p.Arg498Gly | missense_variant | 0.22 |
katG | 2154627 | c.1485T>G | synonymous_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156342 | c.-231G>A | upstream_gene_variant | 0.25 |
katG | 2156348 | c.-237A>G | upstream_gene_variant | 0.25 |
katG | 2156521 | c.-410C>T | upstream_gene_variant | 0.4 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
PPE35 | 2170430 | c.183A>G | synonymous_variant | 0.25 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517965 | c.-150C>G | upstream_gene_variant | 0.12 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519051 | p.Thr313Pro | missense_variant | 0.67 |
kasA | 2519273 | p.Gly387Ser | missense_variant | 0.18 |
eis | 2714634 | c.699C>T | synonymous_variant | 0.17 |
eis | 2714735 | c.598C>T | synonymous_variant | 0.29 |
eis | 2715051 | c.282C>G | synonymous_variant | 0.29 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746543 | c.1056C>G | synonymous_variant | 0.29 |
folC | 2747097 | p.Val168Ile | missense_variant | 0.4 |
folC | 2747132 | p.Thr156Ile | missense_variant | 0.33 |
folC | 2747319 | p.Gly94Ser | missense_variant | 0.2 |
folC | 2747651 | c.-53C>T | upstream_gene_variant | 0.5 |
pepQ | 2859620 | p.Gly267Ser | missense_variant | 0.33 |
ribD | 2986797 | c.-42C>T | upstream_gene_variant | 0.15 |
ribD | 2987095 | p.Gly86Val | missense_variant | 0.14 |
ribD | 2987415 | p.Glu193Lys | missense_variant | 0.15 |
Rv2752c | 3064828 | p.Gly455Asp | missense_variant | 0.4 |
Rv2752c | 3064841 | p.Gly451Ser | missense_variant | 0.22 |
Rv2752c | 3065007 | c.1185G>A | synonymous_variant | 0.5 |
Rv2752c | 3065382 | p.Met270Ile | missense_variant | 0.13 |
Rv2752c | 3065515 | p.Ile226Ser | missense_variant | 0.29 |
Rv2752c | 3065538 | c.654G>A | synonymous_variant | 0.33 |
Rv2752c | 3065545 | p.Ser216Asn | missense_variant | 0.25 |
Rv2752c | 3065646 | c.546C>T | synonymous_variant | 0.2 |
thyX | 3067798 | p.Pro50Ser | missense_variant | 0.13 |
thyA | 3074117 | c.355C>T | synonymous_variant | 0.14 |
thyA | 3074454 | c.18C>T | synonymous_variant | 0.14 |
thyA | 3074492 | c.-21T>C | upstream_gene_variant | 0.29 |
thyA | 3074493 | c.-22C>A | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087749 | c.930C>T | synonymous_variant | 0.14 |
fbiD | 3339099 | c.-19A>G | upstream_gene_variant | 0.12 |
fbiD | 3339135 | c.18C>T | synonymous_variant | 0.12 |
fbiD | 3339246 | c.129C>T | synonymous_variant | 0.33 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448565 | p.Cys21Tyr | missense_variant | 0.25 |
Rv3083 | 3448573 | p.Thr24Ser | missense_variant | 0.33 |
Rv3083 | 3448627 | p.Gly42Ser | missense_variant | 0.13 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448747 | c.244C>A | synonymous_variant | 0.2 |
Rv3083 | 3448825 | p.Glu108Lys | missense_variant | 0.17 |
Rv3083 | 3449230 | p.Gly243Ser | missense_variant | 0.2 |
fprA | 3473888 | c.-119G>A | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474225 | c.219C>T | synonymous_variant | 0.12 |
fprA | 3474252 | c.246G>A | synonymous_variant | 0.15 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612113 | c.1003delG | frameshift_variant | 0.18 |
Rv3236c | 3612169 | c.947delA | frameshift_variant | 0.33 |
Rv3236c | 3612533 | p.Ala195Val | missense_variant | 0.14 |
Rv3236c | 3612664 | c.453G>A | synonymous_variant | 0.5 |
Rv3236c | 3613221 | c.-105C>T | upstream_gene_variant | 0.2 |
Rv3236c | 3613291 | c.-175G>A | upstream_gene_variant | 0.2 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3641048 | p.Phe169Tyr | missense_variant | 0.15 |
fbiB | 3641760 | p.Lys76Glu | missense_variant | 0.12 |
alr | 3840284 | p.Trp379* | stop_gained | 0.12 |
alr | 3840338 | c.1083C>T | synonymous_variant | 0.13 |
alr | 3840380 | p.Met347Ile | missense_variant | 0.17 |
alr | 3840547 | p.Gly292Ser | missense_variant | 0.24 |
alr | 3840619 | p.Asp268Asn | missense_variant | 0.2 |
alr | 3840683 | c.738G>A | synonymous_variant | 0.17 |
alr | 3841229 | c.192G>T | synonymous_variant | 0.22 |
rpoA | 3877558 | p.Pro317His | missense_variant | 0.4 |
rpoA | 3877612 | p.Ile299Asn | missense_variant | 0.13 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.11 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.25 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.33 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.29 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.29 |
rpoA | 3878707 | c.-200C>G | upstream_gene_variant | 0.12 |
clpC1 | 4038198 | p.Gly836Glu | missense_variant | 0.25 |
clpC1 | 4038943 | p.Arg588Trp | missense_variant | 0.13 |
clpC1 | 4039009 | c.1696C>T | synonymous_variant | 0.14 |
clpC1 | 4039034 | c.1671C>T | synonymous_variant | 0.17 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.22 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.11 |
clpC1 | 4040095 | p.Leu204Phe | missense_variant | 0.17 |
clpC1 | 4040331 | p.Val125Ala | missense_variant | 0.13 |
clpC1 | 4040345 | c.360C>T | synonymous_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044437 | c.-156C>T | upstream_gene_variant | 0.29 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240962 | p.Leu367Pro | missense_variant | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241427 | p.Leu522Pro | missense_variant | 0.2 |
embC | 4241665 | c.1803G>A | synonymous_variant | 0.5 |
embC | 4242260 | p.Met800Val | missense_variant | 0.22 |
embA | 4242427 | c.-806A>G | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242962 | p.Gly1034Ser | missense_variant | 0.15 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243715 | c.483C>G | synonymous_variant | 0.2 |
embA | 4244040 | p.Thr270Ala | missense_variant | 0.17 |
embA | 4244048 | c.816C>T | synonymous_variant | 0.15 |
embA | 4244076 | c.847delG | frameshift_variant | 0.11 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244913 | c.1681C>T | synonymous_variant | 0.18 |
embB | 4245719 | c.-795G>A | upstream_gene_variant | 0.25 |
embA | 4245858 | p.Ala876Thr | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246925 | p.Glu138Gln | missense_variant | 0.14 |
embB | 4246944 | p.Gln144Pro | missense_variant | 0.2 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247755 | c.1242C>T | synonymous_variant | 0.25 |
embB | 4247999 | p.Asp496Asn | missense_variant | 0.14 |
embB | 4248575 | p.Phe688Leu | missense_variant | 0.33 |
embB | 4248850 | c.2337G>T | synonymous_variant | 0.22 |
embB | 4249116 | p.Pro868Arg | missense_variant | 0.13 |
embB | 4249596 | p.Trp1028* | stop_gained | 0.22 |
aftB | 4267462 | p.Gln459* | stop_gained | 0.17 |
aftB | 4267506 | p.Asn444Ile | missense_variant | 0.13 |
aftB | 4267512 | p.Leu442Arg | missense_variant | 0.13 |
aftB | 4267528 | p.Ala437Thr | missense_variant | 0.15 |
aftB | 4267554 | p.Asp428Gly | missense_variant | 0.15 |
aftB | 4267637 | c.1200C>T | synonymous_variant | 0.17 |
aftB | 4267862 | p.Tyr325* | stop_gained | 0.12 |
aftB | 4268622 | p.Trp72* | stop_gained | 0.18 |
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 |
ubiA | 4270026 | c.-193C>A | upstream_gene_variant | 0.33 |
ethA | 4327908 | c.-435T>C | upstream_gene_variant | 0.15 |
whiB6 | 4338276 | c.246C>T | synonymous_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 | 4407720 | c.483C>T | synonymous_variant | 0.13 |
gid | 4407796 | p.Ser136Leu | missense_variant | 0.13 |
gid | 4407852 | c.351G>A | synonymous_variant | 0.12 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407964 | p.Ala80Val | missense_variant | 0.2 |
gid | 4408036 | p.Gly56Asp | missense_variant | 0.13 |
gid | 4408079 | p.Gly42Ser | missense_variant | 0.14 |